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Anki Immunosero
Anki Immunosero
/c1 inhibitor
/anaphylatoxin inactivator
/MAC inhibitor
/complement type receptor type 1
(immunecomplex) reactions,
immune complexes are deposited on
(CRI or CD35): CRI binds C3b and C4b and inhibits tissues, causing inflammation.
the amplification loop. what control mechanism?
type I hypersensitivity
/c1 inhibitor type II hypersensitivity
/anaphylatoxin inactivator type III hypersensitivity
/MAC inhibitor type IV hypersensitivity
/complement type receptor type 1
Type III hypersensitivity
complement type receptor type 1
type I hypersensitivity - reaction is
/c1 inhibitor - (C1INH) combines with Clr and Cls (____ or CD35):____ binds C3b and C4b and classified as an immediate
to block Cl activities. A deficiency in C1INH results inhibits the amplification loop. what hypersensitivity reaction because it
in the syndrome hereditary angioedema, an complement receptor? occurs within minutes after reexposure to
autosomal dominant disease. The disease is CS1 an allergen
characterized by unregulated classical pathway CR1
activation, resulting in vascular permeability and CS2 type II hypersensitivity - reaction is
swollen mucous membranes in airways, which can CR2 due to IgG or IgM antibodies
become blocked. directed against cell surface
CR1 antigens
/anaphylatoxin inactivator - This compound
removes a single amino acid from C4a, C3a, and type III
C5a, rendering them useless as anaphylatoxins. hypersensitivity - (immunecomplex)
reactions, immune complexes are
/MAC inhibitor - MAC is not formed because S deposited on tissues, causing
protein binds to C5b-7 complex. inflammation.
EIA
Direct EIA
Indirect EIA
Solid Phase
Direct EIA
1-3% of circulating WBCs
10% of total serum immunoglobulins EIA - Any immunoassay that uses an
enzyme as label. A substrate is added
neutrophils
IgM to measure enzyme activity.
eosinophils
IgG
monocytes
IgE Direct EIA - 1st type of EIA developed.
basophils
IgD Competitive. Enzyme-labeled reagent
lymphocytes
is part of initial ag-ab rxn. All
IgM reactants added at same time. 1
eosinophil
incubation & 1 wash.
neutrophils
2 broad classes of T cells 2 types of phagocytes
eosinophils
monocytes
helper T cells monocyte
basophils
cytotoxic T cells neutrophils
lymphocytes
lymphocytes
ELISA
Sandwich ELISA or capture assay
Rapid ELISA
Ab to HIV. Sensitivity & specificity
Enzyme-multiplied immunoassay technique
comparable to Western blot. Not
(EMIT)
frequently used. Expensive, subjective.
Sandwich ELISA or capture assay
SB
WB
ELISA - Ag attached to solid phase. Ab in
IFA
specimen attaches. Unbound ab removed by
NAAT
washing. Enzyme-labeled antiglobulin
ASO titer begins to increase approximately how
added. Attaches to ab on solid phase.
many days after infection and peaks after 4 to 6 Indirect immunofluorescent assays
Substrate added. Color directly
weeks. (IFA)
proportional to ab concentration. More
2 days
sensitive than competitive EIA. One of most
7 days Western blot (WB) - Ab to
common immunoassays.
14 days HIV. Traditional confirmatory test
21 days but not as sensitive as 4th-gen EIA
Sandwich ELISA or capture assay - Ab
or NAAT.
attached to solid phase. Ag in specimen
7 days
attaches. Enzyme-labeled ab added,
Indirect immunofluorescent assays
attaches to different
(IFA) - Ab to HIV. Sensitivity &
determinant. Enzymatic activity directly
specificity comparable to Western
proportional to amount of ag in sample.
blot. Not frequently used. Expensive,
subjective.
Rapid ELISA - Reagent ag or ab bound to
membrane in single use cassette. Sample
NAAT - HIV RNA. Qualitative test used
added. Presence of ag-ab complex indicated
for confirmation
by colored rxn.
Enzyme-multiplied immunoassay
technique (EMIT) - Ag in specimen &
enzyme-labeled ag compete for binding
sites on reagent ab. When enzyme-labeled ag
binds, enzyme activity inhibited. Enzyme
activity is directly proportional to concentration
of ag in specimen
Absence of these enzymes causes an
accumulation of nucleotide metabolites in all
cells, which is particularly toxic to T and B cells.
what severe combined immune deficiency?
Ab to HIV. Traditional confirmatory test but
-ADA or PNP
not as sensitive as 4th-gen EIA or NAAT.
-Bare lymphocyte syndrome
-Wiskott-aldrich syndrome
WB
IFA Accounts for 15-20% of total serum
-ADA or PNP
NAAT antibody. what immunoglobulin?
Bare lymphocyte syndrome - With
Western blot (WB) IgM
an MHC class II deficiency, T helper cells
IgA
fail to develop. Patients present with
Western blot (WB) - Ab to HIV. Traditional IgG
hypogammaglobulinemia and no CMI response
confirmatory test but not as sensitive as 4th- IgD
gen EIA or NAAT.
Wiskott-aldrich syndrome - Mutation in
IgA
the gene that codes for , a protein involved
Indirect immunofluorescent assays (IFA)
with cytoskeletal reorganization
- Ab to HIV. Sensitivity & specificity IgG - 75%
necessary for delivering cytokines. The
comparable to Western blot. Not frequently IgM - 10%
defect prevents T helper cells from delivering
used. Expensive, subjective.
lymphokines to B cells, macrophages, and other
target cells.
NAAT - HIV RNA. Qualitative test used for
confirmation
ADA or PNP - Absence of these
enzymes causes an accumulation of nucleotide
metabolites in all cells, which is particularly
toxic to T and B cells. what severe combined
immune deficiency?
Ag attached to solid phase. Ab in
specimen attaches. Unbound ab removed
by washing. Enzyme-labeled antiglobulin
added. Attaches to ab on solid phase.
Acute, chronic, or previous infection. Pos Substrate added. Color directly
should be confirmed by recombinant proportional to ab concentration. More
Acute or chronic infection. HDV is a defective
immunoblot assay (RIBA) or molecular sensitive than competitive EIA. One of
virus that can only occur in presence of HBV.
method most common immunoassays. what
EIA?
HBV DNA
HBV DNA
Hepatitis C Anti-HCV
Hepatitis C Anti-HCV ELISA
HCV RNA
HCV RNA Sandwich ELISA or capture assay
Hepatitis D (delta hepatitis)
Hepatitis D (delta hepatitis) Rapid ELISA
IgM anti-HDV
IgM anti-HDV Enzyme-multiplied immunoassay
IgG anti-HDV
IgG anti-HDV technique (EMIT)
HDV RNA
HDV RNA
Hepatitis E
Hepatitis E ELISA
Hepatitis D / (delta hepatitis) IgM anti-HDV
Hepatitis C / Anti-HCV ELISA - Ag attached to solid phase.
Ab in specimen attaches. Unbound
HBV DNA - Current infection. Detectable 21
HBV DNA - Current infection. Detectable 21 ab removed by washing. Enzyme-
days before HBsAg. Used to monitor viral load &
days before HBsAg. Used to monitor viral labeled antiglobulin added. Attaches
therapy.
load & therapy. to ab on solid phase. Substrate added.
Color directly proportional to ab
Hepatitis C / Anti-HCV - Acute, chronic, or
Hepatitis C / Anti-HCV - Acute, chronic, or concentration. More sensitive than
previous infection. Pos should be confirmed by
previous infection. Pos should be confirmed competitive EIA. One of most common
recombinant immunoblot assay (RIBA) or
by recombinant immunoblot assay immunoassays.
molecular method
(RIBA) or molecular method
Sandwich ELISA or capture assay
HCV RNA - Current infection. Used for viral
HCV RNA - Current infection. Used for viral - Ab attached to solid phase. Ag in
load testing, blood/organ donor screening. HCV
load testing, blood/organ donor screening. specimen attaches. Enzyme-labeled ab
genotyping to determine optimal treatment.
HCV genotyping to determine optimal added, attaches to different determinant.
treatment. Enzymatic activity directly
Hepatitis D / (delta hepatitis) IgM anti-
proportional to amount of ag in
HDV - Acute or chronic infection. HDV is a
Hepatitis D . (delta hepatitis) IgM anti- sample.
defective virus that can only occur in
HDV - Acute or chronic infection. HDV is a
presence of HBV.
defective virus that can only occur in Rapid ELISA - Reagent ag or ab
presence of HBV. bound to membrane in single use
IgG anti-HDV - Recovery or chronic
cassette. Sample added. Presence of ag-
infection. Marker of active viral replication.
IgG anti-HDV - Recovery or chronic ab complex indicated by colored rxn.
Used to monitor therapy.
infection. Marker of active viral
replication. Used to monitor therapy. Enzyme-multiplied immunoassay
HDV RNA - Current infection
technique (EMIT) - Ag in specimen
HDV RNA - Current infection & enzyme-labeled ag compete for
binding sites on reagent ab. When
enzyme-labeled ag binds, enzyme activity
inhibited. Enzyme activity is directly
proportional to concentration of ag in
specimen
Ag in specimen & enzyme-labeled ag
compete for binding sites on reagent ab.
When enzyme-labeled ag binds, enzyme activity
inhibited. Enzyme activity is directly proportional to
concentration of ag in specimen. what EIA?
ELISA
Sandwich ELISA or capture assay
Rapid ELISA
Enzyme-multiplied immunoassay technique (EMIT)
neoplasm
benign tumor
malignant tumor
metastatic tumor
Although poor response to platelet transfusion
is multifactorial, antibodies to ____ antigens
Also known as antigen-recognition unit. Neoplasm
are the primary cause of immune-mediated
Responsible for Ig specificity.
platelet transfusion refractoriness. which
Neoplasm - An abnormal mass of tissue
class?
constant region that results from the uncontrolled growth
hinge region of normal cells even after the growth
class I HLA
variable region stimulus is removed.
class II HLA
fab fragment
class III HLA
benign tumor - Typically a mild and
class IV HLA
variable region nonprogressive tumor that pushes aside
normal tissue, but does not invade it, as
class I HLA
the tumor expands
-sequestered-antigen theory
-immunologic deficiency theory
-cross reactivity theory
-polyclonal b cell activation
-forbidden-clone theory
An allergen is injected intradermally. example
of type III hypersensitivity
immunologic deficiency theory
-arthus reaction
-immunologic deficiency theory - An
-immune complex disorder(serum sickness)
An amyloid protein is a nonstructural protein individual can make antibodies or reactive
-glomerulonephritis
that becomes insoluble after an alteration in its T cells to an infectious agent that cross
-vasculitis
secondary structure. In amyloidosis, these react with self antigens
proteins accumulate in organs and tissue.
-arthus reaction
-cross reactivity theory - Some
-primary amyloidosis antigens are hidden from the immune
immune complex disorder(serum sickness)
-secondary amyloidosis system during fetal development. When
- Patients develop antibodies against heterologous
-tertiary amyloidosis the tissue is damaged, the "hidden cells"
serum proteins. example of type III hypersensitivity
-quarternary amyloidosis are exposed to the immune system and
antibodies are produced against these
glomerulonephritis - Immune complexes are
primary amyloidosis cells.
deposited on renal glomeruli. example of type III
hypersensitivity
-polyclonal b cell activation - A
number of bacteria and viruses are known
vasculitis - Inflammation of the blood vessel
to nonspecifically stimulate B cells. If
walls. example of type III hypersensitivity
these B cells have activity against self
antigens, an autoimmune disease can
result
-RA
-SLE
-sjorgen syndrome Antibodies are composed of?
-autoimmune hemolytic anemia Antibodies against treponemal antigens and
nontreponemal __________ develop and -two heavy polypeptide chains and two
sjorgen syndrome elicit a cell-mediated and humoral Ir, which light polypeptide chains.
results in the formation of immune complexes. -two heavy polypeptide chains and one
-RA - IgM binds to abnormal IgG light polypeptide chains.
alloantigens -one heavy polypeptide chains and two
-SLE - Chronic, noninfectious inflammatory disease lipoidal antigens light polypeptide chains.
involving many organs hla-antigens -one heavy polypeptide chains and one
cardiolipin antigens (Wasser-mann antigens) light polypeptide chains.
-sjorgen syndrome - An inflammation of
the salivary and lacrimal cardiolipin antigens (Wasser-mann antigens) two heavy polypeptide chains and two
glands causing dryness of the mouth and light polypeptide chains.
eyes. and positive RF, ANA (speckled or diffuse
pattern), anti-SSA, and anti-SSB
Immunofluorescence
Direct fluorescent antibody (DFA)
staining
Indirect fluorescent antibody (IFA) Antibodies to ____ are present in
staining many systemic autoimmune diseases,
Fluorescence polarization immunoassay such as systemic lupus
(FPIA) erythematosus, mixed connective tissue
Antibodies have only one type of light chain or two
disease, and rheumatoid arthritis
light chains?
Immunofluorescence
/ANA
alpha, beta
Immunofluorescence - Antibodies labeled /IgM that binds to the Fc portion of
epsilon, kappa
with a fluorescent dye are used to detect an abnormal IgG. usually detected by latex
omega, delta
antibody or antigen agglutinations
kappa, lambda
/proteinsh that reversibly preipitate at 4C
Direct fluorescent antibody (DFA) /autoantibodies against the salivary
one light chain (kappa or lambda)
staining - Conjugated (fluorescent glands; and positive RF, ANA (speckled or
labeled) reagent antibody reacts with an diffuse pattern), anti-SSA, and anti-SSB
antigen in a clinical sample to form an
antigenantibody complex ANA
EIA
Approximately how many proteins involved in Assays involving antibody-antigen
EIA - Any immunoassay that uses an enzyme as
three separate pathways of activation? reactions are called?
label. A substrate is added to measure enzyme
10
activity.
20 agglutination
30 precipitation
Direct EIA - 1st type of EIA developed.
40 immunoassays
Competitive. Enzyme-labeled reagent is part of
labeled reaction
initial ag-ab rxn. All reactants added at same
time. 1 incubation & 1 wash.
20 immunoassays
Indirect EIA - Noncompetitive EIA. Enzyme-
labeled reagent isn’t involved in initial ag-ab
rxn. 2 incubations & 2 washes. More sensitive than
direct assays. Also known as enzyme-linked
immunosorbent assay (ELISA)
-RA
-SLE
-sjorgen syndrome
-cryoglobulins B cells express surface molecules such as
what cd marker?
SLE
cd 4,8
-RA - IgM binds to abnormal IgG cd 19,20
B cells differentiate into either a ____, whose cd 2, 3
-SLE - Chronic, noninfectious inflammatory disease role is to produce antibody, or a memory B cell cd 25
involving many organs. Associated with
systemic lupus erythematosus (SLE), mixed plasma cell cd 19,20
connective tissue disease
(MCTD), and rheumatoid arthritis (RA). what cd 2,3 - t cell
autoimmune disease? cd 4,8 - helper t cell (2/3 of t cells), ctl
I(1/3 of t cells)
-sjorgen syndrome - An inflammation of cd 25 - activated t cell
the salivary and lacrimal
glands causing dryness of the mouth and
eyes. and positive RF, ANA (speckled or diffuse
pattern), anti-SSA, and anti-SSB
-sequestered-antigen theory
-immunologic deficiency theory
-cross reactivity theory
-polyclonal b cell activation
-forbidden-clone theory
forbidden-clone theory
Because T cells are involved in both humoral- and
cell-mediated responses, individuals with T helper -immunologic deficiency theory - An By complexing with ___, the osmotic
cell deficiencies can have a severe combined individual can make antibodies or reactive T cytolytic reaction is accelerated
immunodeficiency. what immune deficiency? cells to an infectious agent that cross react with
self antigens C9
Cellular immune deficiencies C19
humoral immune deficiencies -cross reactivity theory - Some antigens are C21
systemic immune deficiencies hidden from the immune system during fetal C24
intracellular immune deficiencies development. When the tissue is damaged, the
"hidden cells" are exposed to the immune C9
Cellular immune deficiencies system and antibodies are produced against
these cells.
viruses, fungi
CD4+ are what type lymphocyte? CD8+ are called
Rickettsia, and fungi
viruses, Rickettsia,
helper T cells cytotoxic T cells
viruses, Rickettsia, fungi
class I
Combination of inherited HLA alleles?
class II
class III Components are synthesized in the
haplotype
class IV ____ (what organ?) , except Cl, which is
genotype
synthesized in the epithelial cells of the
class III intestine.
haplotype
class I - Molecules found on nearly every spleen
phenotype - set of observable characteristics of an
nucleated cell surface liver
individual from the interaction of its genotype with
thyroid
the enviroment
class II - Molecules located on the surface of kidney
monocytes, macrophages, B cells,
genotype - Two haplotypes (one from each parent)
activated T cells, dendritic cells, liver
Langerhans' cells, and some epithelial
haplotype - Combination of inherited HLA alleles
cells
HBV DNA
Hepatitis C Anti-HCV
HCV RNA
Hepatitis D (delta hepatitis)
IgM anti-HDV
IgG anti-HDV
HDV RNA
Hepatitis E
HCV RNA
Defect in oxidative pathway (respiratory Derived from mesodermal connective
HBV DNA - Current infection. Detectable 21
pathway) phagocytes use to create tissues
days before HBsAg. Used to monitor viral load &
hydrogen peroxide, which is used to kill
therapy.
bacteria. what neutrophil defect? sarcoma
muscle tissue
Hepatitis C / Anti-HCV - Acute, chronic, or
-chronic granulamatous disease nerve endings
previous infection. Pos should be confirmed by
-mpo
recombinant immunoblot assay (RIBA) or
molecular method
Chronic granulomatous disease sarcoma
HCV RNA - Current infection. Used for viral
load testing, blood/organ donor screening. HCV
genotyping to determine optimal treatment.
EIA
During the latent phase, no antibody is ELISA
produced for about how many days?. During EMIT
Drug of choice is ___ (semisynthetic derivative of this time, the host is producing plasma cells
tetracycline), which one takes a minimum of 4 to 6 that will secrete antibodies ELISA
weeks. for lyme disease. borellia
1-2 days EIA - Any immunoassay that uses an
penicilin 3-5 days enzyme as label. A substrate is added to
doxycycline 5-7 days measure enzyme activity. A substrate is
metronidazole 7-9 days added to measure enzyme activity.
tetrazolium
5-7 days ELISA - Enzyme-labeled reagents are
doxycycline used to detect antigens or
3-5 days - secondary response has a short latent antibodies. Enzyme must be stable,
phase specific, and cannot bind to antigen or
antibody independently. A colorless
substrate is metabolized by the enzyme
into a colored compound. The intensity
of the color is directly proportional
to the amount of enzyme present.
CA19-9
CA-125
CA15-3
AFP
B-HCG
CEA
CA-125
Every heavy chain and light chain consists of?
CA19-9 - aids in diagnosing colon,
-one variable domain and two constant domain.
gastric, hepatobiliary, and
-one variable domain and one or more constant Express surface molecules such as CD2 and
pancreatic cancer.
domain. CD3
-one or more variable domain and one or more B cell
CA-125 - Expressed in most
constant domain. T cell
nonmucinous epithelial ovarian
-two variable domain and one or more constant
tumors.
domain. T cell
CA15-3 - tumor marker for detection
one variable domain and one or more constant
of breast cancer
domain
AFP - liver tumors, and germ cell
tumors such as testicular cancer.
WB
IFA
NAAT
NAAT
HIV causes? HIV infects what CD markers?
Western blot (WB) - Ab to HIV. Traditional
confirmatory test but not as sensitive as 4th-
AIDS CD4
gen EIA or NAAT.
-opsonization
-immune adherence
-chemotaxis
-anaphylatoxins
If a microorganism overwhelms the body’s
-opsonization If specific antibodies have been formed to
natural resistance, a third line of defensive
antigenic stimulation, they are available
resistance exists
Immune adherence - C3b adheres to immune to protect the body against foreign
complexes and surfaces of substances to substances
adaptive immunity
facilitate clearing of these molecules.
acquired immunity
humoral-mediated immunity
adaptive or acquired immunity
anaphylatoxins - C4a, C3a, and C5a cause cell-mediated immunity
nota
basophils and mast cells to release histamine and
also cause smooth muscle contraction and increased humoral-mediated immunity
adaptive or acquired immunity
vascular permeability.
-arthus reaction
-immune complex disorder(serum
sickness)
-glomerulonephritis
Immortal, progressively invasive, CANCER, invades -vasculitis
Immune complex removes complement?
normal tissues
-glomerulonephritis
classic component
carcinoma cell
advance component
malignant cell immune complex disorder(serum
primary component
neoplasm cell sickness) - Patients develop antibodies
secondary component
tumor cell against heterologous serum proteins.
example of type III hypersensitivity
Classic component
malignant cell
glomerulonephritis - Immune
complexes are deposited on renal
glomeruli. example of type III
hypersensitivity
CA19-9
CA-125
CA15-3
AFP
B-HCG Inactivation of complement starts at what
CEA temperature and how mnay min?
In the peripheral blood, this cell is a ____; in
CEA 37°C for 30 min
the tissue, it is a macrophage
56°C for 30 min
CA19-9 - aids in diagnosing colon, gastric, 37°C for 15 min
monocyte
hepatobiliary, and pancreatic cancer. 56°C for 15 min
CA-125 - Expressed in most
nonmucinous epithelial ovarian tumors. 56°C for 30 min
CA15-3 - tumor marker for detection of breast
cancer
AFP - liver tumors, and germ cell tumors
such as testicular cancer.
B-HCG - may be produced by neoplastic cells of
testicular
cancer and various other tumors.
CEA - colon cancer, colitis, pancreatitis, and
prostate cancer.
primary syphylis
secondary syphylis
Inflammation of the blood vessel tertiary syphilis
walls. example of type III hypersensitivity latent stage syphilis
-hashimoto disease
-graves disease
-myasthenia gravis
-multiple sclerosis
-type 1 diabetes
-type 1 diabetes
multiple sclerosis - Considered a
chronic progressive inflammatory disease
with demyelinization of the nerves. Most
patients with MS have increased IgG
concentrations in the cerebrospinal fluid
(CSF). Oligoclonal bands in CSF on
high-resolution electrophoresis are
also indicative of MS, but patients with
other conditions (SLE, viral meningitis,
neurosyphilis, etc.) can have oligoclonal
bands in the CSF. anti myelsin sheat
bands
Polyclonal Hypergammaglobulinemia
Monoclonal Hypergammaglobulinemia
waldenstrom macroglobulinemia
primary amyloidosis
Laboratory findings include positive direct
Laboratory findings include positive direct primary amyloidosis
antiglobulin test and sometimes cold
antiglobulin test and sometimes cold agglutinins
agglutinins. what autoimmune disease?
Monoclonal
-RA Hypergammaglobulinemia - This
systemic lupus erythromatosus
-SLE causes a narrow peak on serum protein
mycoplasma
-sjorgen syndrome electrophoresis.
chronic lymphocytic leukemia
-autoimmune hemolytic anemia
autoimmune hemolytic anemia
multiple myeloma - Laboratory
autoimmune hemolytic anemia findings: Monoclonal gammopathy and
autoimmune hemolytic anemia
plasma cell infiltrate in bone marrow
-RA - IgM binds to abnormal IgG e. Monoclonal immunoglobulins (M
sle - Chronic, noninfectious
-SLE - Chronic, noninfectious inflammatory disease proteins)
inflammatory disease involving many
involving many organs 1) Diagnostic of multiple myeloma,
organs Disease is more likely to occur in
-sjorgen syndrome - An inflammation of Waldenstrom macroglobulinemia, chronic
women than men and in blacks than
the salivary and lacrimal lymphocytic leukemia, or lymphoma
whites. Tissue injury is caused by
glands causing dryness of the mouth and 2) Immunoglobulin type determination is
autoantibodies and immune
eyes. and positive RF, ANA (speckled or diffuse necessary for diagnosis and prognosis.
complexes deposited in the tissues. Depressed
pattern), anti-SSA, and anti-SSB
suppressor T cell function allows production of
primary amyloidosis - Laboratory
antibodies against "self". Associated with
-autoimmune hemolytic anemia - Laboratory findings: Frequent abnormalities of
systemic lupus erythematosus (SLE),
findings include positive direct antiglobulin test and serum immunoglobulins and presence of
mixed connective tissue disease
sometimes cold agglutinins Bence Jones proteins
(MCTD), and rheumatoid arthritis (RA)
waldenstrom macroglobulinemia
- Symptoms: Weakness, fatigue,
headache, and weight loss d. Laboratory
findings: A spike in the beta or gamma
region on serum protein electrophoresis,
increased plasma viscosity, and abnormal
accumulation of lymphoid cells in the
bone marrow and tissues
-lymphocytosis
MAC is not formed because what protein binds MHC located on chromosome number?
-primary amyloidosis
to C5b-7 complex? a mac inhibitor
-multiple myeloma
protein A 6
-waldenstrom macroglobulinemia
protein F 14
protein H 21
Multiple myeloma
protein S 23
Laboratory findings: Monoclonal gammopathy
protein S 6
and plasma cell infiltrate in bone marrow
Monoclonal immunoglobulins (M proteins)
1) Diagnostic of multiple myeloma, Waldenstrom
macroglobulinemia, chronic lymphocytic leukemia,
or lymphoma
2) Immunoglobulin type determination is necessary
for diagnosis and prognosis.
-hashimoto disease
-graves disease
-myasthenia gravis
Noncompetitive EIA. Enzyme-labeled
-multiple sclerosis
reagent isn’t involved in initial ag-
Mutation in the gene that codes for the _______ , -type 1 diabetes
ab rxn. 2 incubations & 2 washes. More
a protein involved with cytoskeletal
sensitive than direct assays. Also known
reorganization necessary for delivering -myasthenia gravis
as enzyme-linked immunosorbent assay
cytokines
(ELISA) . what enzyme immunoassay?
The defect prevents T helper cells from hashimoto disease - Antithyroid
EIA
delivering lymphokines to B cells, antibodies detected include antithyroglobulin,
Direct EIA
macrophages, and other target cells. what antithyroid peroxidase (microsomal antigen),
Indirect EIA
severe combined immune deficiency? and second colloid antigen (CA-2).
Solid Phase
-ADA or PNP graves disease - characterized
Indirect EIA
-Bare lymphocyte syndrome by hyperplasia and diffuse goiter caused
-Wiskott-aldrich syndrome by an autoantibody reacting with thyroid
EIA - Any immunoassay that uses an
receptor on cells that overstimulates
enzyme as label. A substrate is added to
Wiskott-aldrich syndrome the thyroid gland. The autoantibody mimics
measure enzyme activity.
the activity of thyroid-stimulating
Bare lymphocyte syndrome - With an MHC hormone (TSH).
Direct EIA - 1st type of EIA developed.
class II deficiency, T helper cells fail to
Competitive. Enzyme-labeled reagent
develop. Patients present with myasthenia gravis - Neuromuscular
is part of initial ag-ab rxn. All
hypogammaglobulinemia and no CMI response disease in which the nerve muscles do
reactants added at same time. 1
not function normally. Most
incubation & 1 wash.
Wiskott-aldrich syndrome - Mutation in the patients exhibit antibodies to
gene that codes for , a protein involved with acetylcholine receptors. These
Indirect EIA - Noncompetitive
cytoskeletal reorganization necessary for autoantibodies block nerve impulses and can
EIA. Enzyme-labeled reagent isn’t
delivering cytokines. The defect prevents T initiate damage to neurons
involved in initial ag-ab rxn. 2
helper cells from delivering lymphokines to B cells,
incubations & 2 washes. More sensitive
macrophages, and other target cells. multiple sclerosis - Considered a chronic
than direct assays. Also known as
progressive inflammatory disease with
enzyme-linked immunosorbent assay
ADA or PNP - Absence of these demyelinization of the nerves. Most patients
(ELISA)
enzymes causes an accumulation of with MS have increased IgG concentrations in
nucleotide metabolites in all cells, which is the cerebrospinal fluid (CSF). Oligoclonal
Solid phase - Reagent ag or ab
particularly toxic to T and B cells. what severe bands in CSF on high-resolution
bound to support medium, e.g.,
combined immune deficiency? electrophoresis are also indicative of MS, but
polystyrene test tubes, microtiter plates,
patients with other conditions (SLE, viral
cellulose membranes, glass beads.
meningitis, neurosyphilis, etc.) can have
oligoclonal bands in the CSF. anti myelsin
sheat bands
-double immunodiffusion
-electrophoresis
-immunofixation electrophoresis
-countercurrent immunoelectrophoresis
Countercurrent
Numerous evenly distributed stained
immunoelectrophoresis (CIE)
speckles within the nuclei associated with
antibodies to extractable nuclear antigens—
double immunodiffusion - Antigen
Nonspecific response to tissue damage nuclear ribonucleoprotein (RNP) and anti-
and antibody are placed in wells in
Smith (Sm). what Interpretation of indirect
the gel and diffuse toward each
injury immunofluorescence results?
other. When optimum concentrations
bleeding
are met (at the zone of equivalence), a
inflammation -homogenous
precipitate line forms
bruising -peripheral
-speckled
electrophoresis - Separate molecules
inflammation -nucleolar
according to their electrical charge
-centromere
immunofixation
-speckled
electrophoresis - Serum, urine, or
CSF is electrophoresed. type of
precipitation reaction. Detects
the presence of an immunoglobulin in
serum or urine
countercurrent
immunoelectrophoresis - On an agar
gel plate or slide, antigen is added to
one well and antibody is added to
another well. An electric current
accelerates the movement of the
antigen and antibody toward each
other, resulting in precipitation sooner
than if an electric current is not applied.
type of precipitation reactio
hypersensitivity reaction
type I hypersensitivity reaction
type II hypersensitivity reaction
type III hypersensitivity reaction PMNs adhere to activated ____ to move
between to go to the site of tissue damage
hypersensitivity reaction
tissue cells PRRs are found in
type I hypersensitivity - reaction is classified as endothelial cells
an immediate hypersensitivity reaction because smooth muscle cells plants and animals
it occurs within minutes after reexposure to an fibrins
allergen
endothelial cells
type II hypersensitivity - reaction is due to IgG
or IgM antibodies directed against cell
surface antigens
-turbidimetry
-nephelometry
-Fluid-phase precipitation
-precipitation reactions in agar gel
-rocket immunoelectrophoresis Patients present with small amounts or
-Immunofixation electrophoresis absence of serum and secretory IgA.
Patients develop antibodies against
what humoral immune deficiency?
heterologous serum proteins. example of type
Fluid-phase precipitation
III hypersensitivity
-Bruton X-linked agammaglobulinemia
turbidimetry - is the measurement of light -Hyper-IgM syndrome
-arthus reaction
transmitted through a suspension of -Selective IgA deficiency
-immune complex disorder(serum sickness)
particles -Ataxia-telangiectasia
-glomerulonephritis
-vasculitis
nephelometry - is a direct measure of light -Selective IgA deficiency
scattered by particles suspended in solution
-immune complex disorder(serum sickness)
-Bruton X-linked
Fluid-phase precipitation - Passive diffusion agammaglobulinemia - marked
immune complex disorder(serum
of soluble antigen and antibody deficiency of all classes of
sickness) - Patients develop antibodies against
immunoglobulins is detected after
heterologous serum proteins. example of type
precipitation reactions in agar gel - Antigen about 6 months of age
III hypersensitivity
and antibody diffuse through the agar gel and
precipitate when they reach the zone of -Ataxia-telangiectasia - defect in a
glomerulonephritis - Immune complexes
equivalence. Molecular size determines the speed of kinase gene that regulates the cell
are deposited on renal glomeruli. example of
travel through the gel. cycle. The B and T helper cells are
type III hypersensitivity
affected.
rocket immunoelectrophoresis - Used to
vasculitis - Inflammation of the blood vessel
quantify antigens. Antigens are electrophoresed -hyper-IgM syndrome = X-linked
walls. example of type III hypersensitivity
in agar-containing antibody. A pH is selected so that genetic disease. what humoral immune
the antibodies are immobile. deficiency
height of the rocket is proportional to the
concentration of antigen in the specimen.
immunofixation electrophoresis - Serum,
urine, or CSF is electrophoresed. type of
precipitation reaction. Detects the presence of an
immunoglobulin in serum or urine
Reagent ag or ab bound to
membrane in single use cassette.
Sample added. Presence of ag-ab
Reagent ag on glass slide overlaid with
complex indicated by colored
patient serum. If corresponding ab present in
rxn. what EIA?
serum, attaches to ag. When fluorescein-labeled
antihuman globulin added, attaches to ab.
ELISA
Fluorescence observed with fluorescent
Sandwich ELISA or capture assay
microscope. what method?
Rapid ELISA
Enzyme-multiplied immunoassay
Direct fluorescent antibody (DFA)
technique (EMIT)
staining
Indirect fluorescent antibody (IFA)
Rapid ELISA
staining
Fluorescence polarization immunoassay
ELISA - Ag attached to solid phase.
(FPIA)
Ab in specimen attaches. Unbound ab
removed by washing. Enzyme-
Indirect fluorescent antibody (IFA)
Reagent ab attached to carrier bacteria. labeled antiglobulin added. Attaches
staining
(Staphylococcus aureus most frequently used as to ab on solid phase. Substrate
carrier). rapid id of bacteria. what agglutination added. Color directly proportional to
Direct fluorescent antibody (DFA)
method? ab concentration. More sensitive than
staining - Specimen on glass slide
competitive EIA. One of most common
overlaid with fluoresceinlabeled ab. If
agglutination immunoassays.
corresponding ag present, labeled ab binds.
hemeagglutination
Fluorescence observed with fluorescent
coagglutination Sandwich ELISA or capture
microscope.
biagglutination assay - Ab attached to solid phase. Ag in
specimen attaches. Enzyme-labeled ab
Indirect fluorescent antibody (IFA)
coagglutination added, attaches to different
staining - Reagent ag on glass slide
determinant. Enzymatic activity
overlaid with patient serum. If
directly proportional to amount of
corresponding ab present in serum, attaches to
ag in sample.
ag. When fluorescein-labeled antihuman
globulin added, attaches to ab. Fluorescence
Rapid ELISA - Reagent ag or ab
observed with fluorescent microscope.
bound to membrane in single use
cassette. Sample added. Presence of ag-
Fluorescence polarization immunoassay
ab complex indicated by colored rxn.
(FPIA) - Labeled ag competes with ag in
specimen for sites on reagent ab. Free
Enzyme-multiplied immunoassay
labeled ag rotates rapidly, emits little polarized
technique (EMIT) - Ag in specimen
light. Bound labeled ag rotates more slowly,
& enzyme-labeled ag compete for
emits more polarized light. Amount of polarized
binding sites on reagent ab. When
light is inversely proportional to concentration
enzyme-labeled ag binds, enzyme activity
of ag in specimen.
inhibited. Enzyme activity is directly
proportional to concentration of ag in
specimen
Recovery or chronic infection. Marker
of active viral replication. Used to
monitor therapy.
HBV DNA
Hepatitis C Anti-HCV
HCV RNA
Reagent ag or ab bound to support medium, Hepatitis D (delta hepatitis)
e.g., polystyrene test tubes, microtiter plates, IgM anti-HDV
cellulose membranes, glass beads. what enzyme IgG anti-HDV
immunoassay? HDV RNA
EIA Hepatitis E
Direct EIA
Indirect EIA IgG anti-HDV
Solid Phase
HBV DNA - Current
Reagin antibodies are formed after exposure to
Solid phase infection. Detectable 21 days before
Treponema pallidum and react with lipoidal
HBsAg. Used to monitor viral load &
antigens used in screening tests for syphilis. test
EIA - Any immunoassay that uses an enzyme as therapy.
for syphilis?
label. A substrate is added to measure
enzyme activity. Hepatitis C / Anti-HCV - Acute,
RPR
chronic, or previous infection. Pos should
VDRL
Direct EIA - 1st type of EIA developed. be confirmed by recombinant
FTA-ABS
Competitive. Enzyme-labeled reagent is part of immunoblot assay (RIBA) or molecular
TP-PA
initial ag-ab rxn. All reactants added at same method
NAD
time. 1 incubation & 1 wash.
HCV RNA - Current infection. Used for
nontreponemal antibody detection
Indirect EIA - Noncompetitive EIA. Enzyme- viral load testing, blood/organ donor
labeled reagent isn’t involved in initial ag-ab screening. HCV genotyping to determine
rxn. 2 incubations & 2 washes. More sensitive than optimal treatment.
direct assays. Also known as enzyme-linked
immunosorbent assay (ELISA) Hepatitis D . (delta hepatitis) IgM
anti-HDV - Acute or chronic
Solid phase - Reagent ag or ab bound to infection. HDV is a defective virus
support medium, e.g., polystyrene test tubes, that can only occur in presence of
microtiter plates, cellulose membranes, glass beads. HBV.
Anti-DNAse B (AD-B)
SLO is added to serial dilutions of patient
ASO neutralization test
serum, along with group O RBCs as indicator
ASO rapid latex agglutination test
cells. If the patient serum contains antibodies
Streptozyme
against SLO, the antibodies will complex with
culture
the corresponding antigens
Streptozyme
-streptolysin O
-streptolysin S
Anti-DNAse B (AD-B) - Streptococci
-streptolysin A
produce the enzyme deoxyribonuclease.
-ASO titer
Responsible for nonspecific response ASO neutralization test - Streptolysin
Antistreptolysin O (ASO) titer
-immune system O is a hemolysin produced by most beta-
-myeloid cells hemolytic group A streptococci. Infected
-streptolysin O - oxygen-labile
-leukocytes individuals produce antibody to
enzyme that causes hemolysis by binding to
-granulocytes Streptolysin O. The classic ASO test is a
cholesterol in the RBC membrane
neutralization assay. Antibodies to
myeloid cells Streptolysin O prevent hemolysis.
-streptolysin S - is a nonantigenic,
oxygen-stable enzyme. It causes hemolysis
ASO rapid latex agglutination test
by disrupting the selective permeability of the
- Latex particles coated with Streptolysin
RBC membrane.
O agglutinate when mixed with patient's
serum containing ASO antibody
-ASO - SLO is added to serial dilutions of
patient serum, along with group O RBCs as
Streptozyme - Screening test produced
indicator cells. If the patient serum contains
by Wampole Laboratories (Cranbury,
antibodies against SLO, the antibodies will
New Jersey) that detects antibodies to five
complex with the corresponding antigens
S. pyogenes proteins: DNase B,
hyaluronidase, NADase, streptokinase,
and Streptolysin
O. Principle: Streptozyme is a passive
hemagglutination assay. Newer methods
use latex as the earner particle.
Immunonephelometry assays are also
available.
-turbidimetry
-nephelometry
-Fluid-phase precipitation
-precipitation reactions in agar gel
-rocket immunoelectrophoresis
-Immunofixation electrophoresis
Secondary tumor derived from a malignant primary
tumor Immunofixation electrophoresis
immunofixation
electrophoresis - Serum, urine, or CSF
is electrophoresed. type of precipitation
reaction. Detects the presence of an
immunoglobulin in serum or urine
Some antigens are hidden from the immune
system during fetal development. When the
tissue is damaged, the "hidden cells" are
exposed to the immune system and antibodies
are produced against these cells. what
autoimmune theory?
-sequestered-antigen theory
-immunologic deficiency theory
Soluble antigen and soluble antibody react to form -cross reactivity theory Some mediators that act between
an insoluble product -polyclonal b cell activation leukocytes are called
-forbidden-clone theory -interferon
agglutination -TNF
precipitation sequestered-antigen theory -interleukins
hemolysis
cross reactivity -immunologic deficiency theory - An interleukins
labeled reaction individual can make antibodies or reactive T
cells to an infectious agent that cross react with interferon - family of proteins
precipitation reaction self antigens produced rapidly by many cells in
response to viral infection
agglutination -Soluble antibody reacts with -cross reactivity theory - Some antigens are
insoluble antigen or soluble antigen reacts hidden from the immune system during fetal Interleukins - Some mediators that
with insoluble antibody development. When the tissue is damaged, the act between leukocytes
"hidden cells" are exposed to the immune
precipitation - Soluble antigen and soluble system and antibodies are produced against TNF - is a multifunctional
antibody react to form an insoluble product these cells. cytokine that plays important roles
in diverse cellular events such as cell
labeled reaction - A label producing a measurable -polyclonal b cell activation - A number of survival, proliferation,
end product is attached to an antibody or antigen bacteria and viruses are known to differentiation, and death
nonspecifically stimulate B cells. If these B cells
have activity against self antigens, an
autoimmune disease can result
ASO neutralization test - Streptolysin O is a ASO neutralization test - Streptolysin O is a Subcutaneous injection of tuberculosis
hemolysin produced by most beta-hemolytic group hemolysin produced by most beta-hemolytic antigen is used as a diagnostic skin test.
A streptococci. Infected individuals produce group A streptococci. Infected individuals what test?
antibody to Streptolysin O. The classic ASO test is a produce antibody to Streptolysin O. The classic
neutralization assay. Antibodies to Streptolysin O ASO test is a neutralization assay. Antibodies to -arthus reaction
prevent hemolysis. Streptolysin O prevent hemolysis. -spot test
-Tuberculin-type hypersensitivity
ASO rapid latex agglutination test - Latex ASO rapid latex agglutination test - Latex -type III hypersensitivity test
particles coated with Streptolysin O agglutinate particles coated with Streptolysin O agglutinate
when mixed with patient's serum containing ASO when mixed with patient's serum containing Tuberculin-type hypersensitivity
antibody ASO antibody
primary syphylis
secondary syphylis
tertiary syphilis
latent stage syphilis
congenital syphilis
Syphilis is easily and effectively treated. _____
T cell proliferation occurs in the ___ and
is the drug of choice, although tetracycline or
congenital syphilis maturation lasts for __
erythromycin can also be used. treatment?
primary syphylis - Inflammatory lesions thymus, 2 months
tetracyclin
(chancres) appear 2 to 8 weeks. thymus, 3 months
penicilin
bone marrow, 2months
metronidazole
tertiary syphilis - characterized by bone marrow, 3 months
tylenol
granulomatous lesions known as gummata. These
lesions may develop in skin. thymus, 3 months
Penicillin
latent stage syphilis - syphilis is contagious and
is generally considered to begin after the second
year of infection. There are no clinical symptoms,
although serologic tests are still positive.
The affinity for multivalent antigens and multiple The antigen has been affixed or absorbed
antibodies to combine; the extent of binding to the particle size. used for Rheumatoid
capacity factor, antinuclear antibody. what
agglutination method?
avidity
affinity direct agglutination
peptide bond indirect agglutination
electrostatic bond passive aggluination
specificity active agglutination
cross reactivity
indirect agglutination
avidity
reverse passive agglutination - A The classic pathway has three major
avidity - The affinity for multivalent antigens and technique in which an antibody is stages:'
multiple antibodies to combine; the extent of attached to a particle, producing
binding capacity. This is greater than the cumulative agglutination with a specific soluble 1. Recognition
affinity constants for all antigenantibody pairs. antigen 2. Amplification of proteolytic
complement cascade
affinity - The strength of the interaction between a passive agglutination - indirect 3. Membrane attack complex (MAC)
single antibody binding site and a single epitope agglutination is also called passive
agglutination. A technique in which soluble read and skip
electrostatic bond - Positively charged portions antigen is attached to a particle,
of one molecule are attracted to negatively charged producing agglutination with a specific read and skip
portions of another molecule.This bonding is soluble antibody
affected by the pH and ionic strength of the
environment. direct agglutination - This method
uses antigens naturally occurring on a
specificity - refers to the antibody's greatest particle to demonstrate agglutination. also
affinity for a particular antigen. Widal test for typhoid fever. Salmonella O & H
ags used to detect abs in patient serum.
cross reactivity - occurs when the antibody
combines with an antigen that is structurally similar indirect agglutination - The antigen has
to the immunogen that stimulated the antibody been affixed or absorbed to the particle
production or the antigen the antibody has the size. used for Rheumatoid factor,
greatest affinity for antinuclear antibody
The highest CEA levels are found in what The major cellular component of acquired
The first time a graft is encountered. the immune
disease? immunity is what wbc?
system attacks and ultimately destroys (rejects) the
nonself tissue.
tumor neutrophil
carcinoma disease monocyte
first graft rejection
neoplasm disease lymphocyte
second graft rejection
metastatic disease plasma cell
first graft rejection
metastatic disease lymphocyte
The presence of ___ within the same complex may The problem is that every organism has a limit The production of earwax or called the
account for its tendency to polymerize and form as to the number of genes it can encode in its ___ protects the auditory canals from
small protein micelles infectious disease.
avidity
affinity
peptide bond
electrostatic bond
specificity
cross reactivity
affinity
isograft isograft
Transmission of Lyme Disease is spread
allograft allograft
by the bite of infected ticks of the genus
xenograft xenograft
____. The preferred host for both the
autograft autograft
larval and nymphal life cycle of tick is the
white footed mouse.
xenograft autograft
-rubella
allograft - tissue from a genetically different allograft - tissue from a genetically different
-ixodes
member of the same species, such as a human member of the same species, such as a human
-coxsackie
kidney) kidney)
-burellia
isograft - Transfer of tissue between genetically isograft - Transfer of tissue between
identical individuals genetically identical individuals
ixodes
autograft - Transfer of tissue from one site to autograft - Transfer of tissue from one site to
another within an individual another within an individual
xenograft - Transfer of tissue between two xenograft - Transfer of tissue between two
individuals of different species individuals of different species
-turbidimetry
-nephelometry
-Fluid-phase precipitation
-precipitation reactions in agar gel
-rocket immunoelectrophoresis
-Immunofixation electrophoresis
rocket immunoelectrophoresis
immunofixation electrophoresis - Serum,
urine, or CSF is electrophoresed. type of
precipitation reaction. Detects the presence of an
immunoglobulin in serum or urine
When oncogenes are deregulated, the protein
product can lead to tumor formation. Proto-
oncogenes are found in nearly all nucleated cells,
With an MHC class II deficiency, T helper
from yeast to human, and are involved in cell
cells fail to develop. Patients present with X-linked genetic disease. Affected
growth. Alteration in gene expression or protein
hypogammaglobulinemia and no CMI response. individuals often have autoantibodies to
structure can initiate. what tumor associated
what severe combined immune deficiency? platelets, red blood cells, and
antigen?
neutrophils. Affected individuals are
-ADA or PNP prone to respiratory tract infections. what
Tumor-specific peptides
-Bare lymphocyte syndrome humoral immune deficiency?
virus-induced tumors
-Wiskott-aldrich syndrome
genome-encoded tumor antigens
-Bruton X-linked agammaglobulinemia
oncofetal antigens
-Bare lymphocyte syndrome -Hyper-IgM syndrome
-Selective IgA deficiency
genome-encoded tumor antigens
Bare lymphocyte syndrome - With -Ataxia-telangiectasia
an MHC class II deficiency, T helper cells
Tumor-specific peptides - are intracellular
fail to develop. Patients present with -Hyper-IgM syndrome
proteins expressed on the surface of a tumor due to
hypogammaglobulinemia and no CMI response
interaction with MHC class I and class II molecules.
-Bruton X-linked agammaglobulinemia
Wiskott-aldrich syndrome - Mutation in - marked deficiency of all classes of
virus-induced tumors - Tumors caused by
the gene that codes for , a protein involved immunoglobulins is detected after
viruses usually have viral antigens on their surface
with cytoskeletal reorganization about 6 months of age
necessary for delivering cytokines. The
genome-encoded tumor antigens - When
defect prevents T helper cells from delivering -Ataxia-telangiectasia - defect in a
oncogenes are deregulated, the protein product can
lymphokines to B cells, macrophages, and other kinase gene that regulates the cell
lead to tumor formation. Proto-oncogenes are found
target cells. cycle. The B and T helper cells are
in nearly all nucleated cells, from yeast to human,
affected.
and are involved in cell growth. Alteration in gene
ADA or PNP - Absence of these
expression or protein structure can initiate
enzymes causes an accumulation of nucleotide -hyper-IgM syndrome = X-linked
metabolites in all cells, which is particularly genetic disease. what humoral immune
oncofetal antigen -are produced during fetal
toxic to T and B cells. what severe combined deficiency
development but present in minute amounts after
immune deficiency?
birth. However, they may become expressed after
malignant transformation (e.g., a-fetoprotein and
carcinoembryonic antigen).
___ are coated with Streptolysin O agglutinate
when mixed with patient's serum containing
ASO antibody. what test?
Anti-DNAse B (AD-B)
ASO neutralization test
ASO rapid latex agglutination test
Streptozyme
culture
_____ are a group of microbial infections _____ of the antibody is located at the _____ with infected persons is the most
characterized by fever and the production of carboxy-terminus. It is responsible for common form of transmission of human
antibodies known as _____ agglutinins the biological activity of the molecule, syphilis?
including activating complement
-febrile diseases, febrile FaB sexual contact
-echinosis, febrile FC infected food
-enteriobacteriaceae, cold agglutinins Heavy Chain aerosol droplets
-gram positive bacteria, warm agglutinins Light Chain fecal contamination
haptoglobin
hapten
adjuvant
epitope
immunogen a more recently eveloved mechanism that
a heat-labile series of 18 plasma proteins???
allows the body to recognize, remember,
hapten respond to a specific antigen
cytokines
complement
hapten - a low-molecular-weight molecule that acquired or adaptive immunity
lysozymes
alone is too small to stimulate an immune natural or innate immunity
opsonins
response but can combine with another passive immunity
molecule to induce a response.
complement
acquired or adaptive immunity
adjuvant - compound that enhances an
immune response
-allotypes
-idiotypes
-isotypes
a series of biochemical and
a part of the genetic system which causes malignant Idiotypes cellular changes that facilitate ____
tumours to develop (engulfment and destruction) of
mutant forms of proto-oncogenes that contribute to -allotypes - term used to describe unique microorganisms or damaged cells
various tumor types or malignant transformation differences within constant region of gamma
and alpha heavy chain and kappa light chains digestion
proto-oncogenes present in different individuals. Species lysis
oncogenes specific variations in the constant domains of precipetation
heavy or light chains phagocytosis
oncogenes
-idiotypes - a result of the unique structures phagocytosis
on light and heavy chains individual
determinants characteristics of each antibody.
Variation in the variable region
th1 cells
a toxin or other foreign substance that
th2 cells a surface marker that identifies a particular
induces an immune response in the
th3 cells linaeage or differentiation stage with a define
body. are substances that are recognized
th4 cells structure and that can be identified with a
as foreign by the body and, therefore,
group of MABs
elicit immune responses.
th1 cells
HLA
antibody
th1 cells - a subset of T helper cells, that secrete MHA
antigen
cytokines that activate other cells involved in CD
immunogen
the response LA
allogen
th2 cells - release cytokines that are required
for B cell differentiation. activate immune CD (cluster of differentiaiton)
antigen
response
th1 and 2 - can promote the development of
cytotoxic cells believed to be develop from
Th0 cells
malignancy
metastasis
a typical monomeric IgG molecule consists of three cancer
a unique substnace that builds up aliphophilic
globular regions ____ linked by a flexible hinge aplastic
complex in all membranes from several
region proteins
metastasis
Fc pair MAST
malignancy - Cancers can exert a
2 Fab regions MAC
suppressive effect on the immune system.
Fc' + F(ab)2 complement
Impairment of antibody production is
2 Fab regions and an Fc pair antibodies
found in lymphomas, chronic lymphocytic
leukemia, and multiple myeloma
2 Fab regions and an Fc pair MAC
carcinoma - Tumors that arise from
endodermal or ectodermal tissue
lymph nodes
spleen
MALT
aids in diagnosing colon, gastric,
peyers patch adhering to the membranes of the nose and
hepatobiliary, and pancreatic
nasopharynx traps microorganisms
cancer.
spleen
earwax
CA19-9
lymph nodes - where B cells migrate to the cortex cerumen
CA-125
and T cells to the paracortex sebum
CA15-3
ear bone
AFP
spleen - Purpose: Filter blood. Contains both T and mucus
B-HCG
B cells cellular barrier
CEA
MALT - Found in submucosa in gastrointestinal mucus
ca19-9
tract, respiratory tract, and urogenital tract. These
surfaces interact with the environment and can
begin the immune response early
Hepatitis B surface antigens (HBsAg) Hepatitis B surface antigens (HBsAg) Hepatitis B surface antigens
- appear 1 week to 2 months after (HBsAg) - appear 1 week to 2
Hepatitis B surface antigens (HBsAg) exposure, and approximately 2 weeks to 2 months after exposure, and
- appear 1 week to 2 months after exposure, months before the onset of symptoms. HBsAg approximately 2 weeks to 2 months before
and approximately 2 weeks to 2 months before the disappears during the convalescent phase of the onset of symptoms. HBsAg disappears
onset of symptoms. HBsAg disappears during the acute disease and is an indicator of acute during the convalescent phase of acute
convalescent phase of acute disease and is an infection or chronic infection with disease and is an indicator of acute
indicator of acute infection or chronic unresolved antigenemia. infection or chronic infection with
infection with unresolved antigenemia. unresolved antigenemia.
Hepatitis B surface antibodies (HBsAb)
Hepatitis B surface antibodies (HBsAb) - appear as the antigens disappear. The Hepatitis B surface antibodies
- appear as the antigens disappear. The presence of these antibodies indicates (HBsAb) - appear as the antigens
presence of these antibodies indicates recovery recovery and lifelong immunity. disappear. The presence of these
and lifelong immunity. antibodies indicates recovery and
Hepatitis B core antibodies (HBcAb) lifelong immunity.
Hepatitis B core antibodies (HBcAb) - appear shortly after the surface
- appear shortly after the surface antigens antigens appear. At this time, the ALT levels Hepatitis B core antibodies
appear. At this time, the ALT levels begin to rise. begin to rise. HBcAb persist throughout life (HBcAb) - appear shortly after the
HBcAb persist throughout life and are a and are a marker for previous infection. surface antigens appear. At this time,
marker for previous infection. the ALT levels begin to rise.
Hepatitis Be antigen - appears before the HBcAb persist throughout life and
Hepatitis Be antigen - appears before the onset of clinical disease, after the are a marker for previous infection.
onset of clinical disease, after the appearance of the surface antigens, and
appearance of the surface antigens, and disappears within approximately 2 Hepatitis Be antigen - appears
disappears within approximately 2 weeks. weeks. The presence of the Be before the onset of clinical disease,
The presence of the Be antigen indicates active antigen indicates active viral after the appearance of the surface
viral antigens, and disappears within
approximately 2 weeks. The presence
of the Be antigen indicates active viral
Tumor-specific peptides
virus-induced tumors
genome-encoded tumor antigens
oncofetal antigens
Tumor-specific peptides
are exerted by the interaction of antibody with
complement and the phagocytic cells (natural
Tumor-specific peptides - are intracellular
immunity) and of T cells with macrophages are measured to indicate consumption
proteins expressed on the surface of a tumor
and follow disease states. what are these
due to interaction with MHC class I and class II
-humoral-mediated immunity and lymphocytic complements?
molecules.
mediated immunity C1
-humoral-mediated immunity and cell C2 and C3
virus-induced tumors - Tumors caused by
mediated immunity C3 and C4
viruses usually have viral antigens on their
-cellular-mediated immunity C4
surface
-humoral-mediated immunity
C3 and C4
genome-encoded tumor antigens - When
humoral-mediated immunity and cell
oncogenes are deregulated, the protein product
mediated immunity
can lead to tumor formation. Proto-oncogenes
are found in nearly all nucleated cells, from
yeast to human, and are involved in cell growth.
Alteration in gene expression or protein
structure can initiate
Tumor-specific peptides
virus-induced tumors
genome-encoded tumor antigens
oncofetal antigens
Tumor-specific peptides
Hepatitis E
positive selection
negative selection
positive and negative selection breaks antibodies in the hinge region
breaks antibodies below the hinge region
double negative
papain
papain
positive and negative selection pepsin
pepsin
positive selection - clones able to recognize papain
pepsin
and react to foreign antigen.
negative selection - purging of clones able to pepsin = breaks antibodies below the
papain = breaks antibodies in the hinge region
interact with self-antigens in a damaging way hinge region
positive and negative selection - body checks
if the receptor is automimmune
double negative - positive selection for
ability to recognize antigen
Th1
Th2
can only connect to virus antigens on the oustide of
Th1 and Th2 cause dilation of blood cells
the infected cell
nota
complement
B cells
Th1 and Th2 heparin
T cells
histamine
B and T cells
th1 cells - a subset of T helper cells, cytokines
nota
that secrete cytokines that activate other
cells involved in the response histamine
T cells
th2 cells - release cytokines that are
required for B cell differentiation.
activate immune response
th1 and 2 - can promote the development
of cytotoxic cells believed to be develop
from Th0 cells
-hashimoto disease
-graves disease
-myasthenia gravis
-multiple sclerosis
-type 1 diabetes
-hashimoto disease
-graves disease
-myasthenia gravis
-multiple sclerosis
-type 1 diabetes
clones able to recognize and react to
-multiple sclerosis
foreign antigen.
hashimoto disease - Antithyroid
-positive selection
antibodies detected include antithyroglobulin,
-negative selection
antithyroid peroxidase (microsomal antigen), and
-positive and negative selection
second colloid antigen (CA-2).
-double negative
classical pathway wont activate if there is
graves disease - characterized by hyperplasia
positive selection
and diffuse goiter caused by an autoantibody no antibodies
reacting with thyroid receptor on cells that no antigens
positive selection - clones able to
overstimulates the thyroid gland. The no bacteria
recognize and react to foreign
autoantibody mimics the activity of thyroid- no viruses
antigen.
stimulating hormone (TSH).
negative selection - purging of
no antibodies
clones able to interact with self-antigens
myasthenia gravis - Neuromuscular disease
in a damaging way
in which the nerve muscles do not function
positive and negative
normally. Most patients exhibit antibodies to
selection - body checks if the
acetylcholine receptors. These autoantibodies
receptor is automimmune
block nerve impulses and can initiate damage to
double negative - positive selection
neurons
for ability to recognize antigen
multiple sclerosis - Considered a chronic
progressive inflammatory disease with
demyelinization of the nerves. Most patients with
MS have increased IgG concentrations in the
cerebrospinal fluid (CSF). Oligoclonal bands in
CSF on high-resolution electrophoresis are
also indicative of MS, but patients with other
conditions (SLE, viral meningitis, neurosyphilis,
etc.) can have oligoclonal bands in the CSF. anti
myelsin sheat bands
proteinase
common finding of this disease Exophthalmos protease
(bulging eyes) and infiltrative dermopathy. what properdin complement protein
organ-specific autoimmune disease? nbt
c1
Hashimoto’s proteinase c2
Goodpasture Syndrome c3
graves disease proteinase - complement many of which are c4
multiple myeloma enzymes are called????
protease - proteins from the cleavage of a C3
graves disease larger precurose by a
properdin - substances that stabilizes the
C3bBb complex
nbt - test used in order to confirm CBD in
patient
compoenents of innate immunity but not
cellular, belong to humoral component
T lymphocytes, B lymphocytes,
plasma cells -cellular components are
the adaptive immune system
-CRP
-haptoglobin
-fibrinogen
-a1-antitrypsin
-ceruloplasmin
-a2-macroglobulin
CRP
consists of a heterodimer and a number of
compound that enhances an immune response. It is -CRP - concentration increases several
associated polypeptides that form CD3
not immunogenic and cannot induce an antibody hundred times after injury
complex
response alone.
-haptoglobin - removes free hemoglobin from
TCR
opsonin circulation
TCT
adjuvant
TCH
antigen -fibrinogen - is found in increased quantities
TCC
at the site of an injury; it is converted to fibrin
adjuvant to heal the injury
TCR
-a1-antitrypsin - is a family of serine protease
inhibitors synthesized in the liver. Deficiency
causes premature loss of elasticity in the
lung and liver damage
-ceruloplasmin
Interleukins - Some mediators that act q fever, rocky mountain spotted fever NADPH Oxidase
between leukocytes
first complement in the protein is activated in first graft rejection occurs how many days
first antibody produced during infection
classical pathway after transplantation?
IgM
c1 2 days
IgG
c2 7 days
IgD
c3 10-14 days
IgE
c4 16 days
IgM
C1 10-14 days
function of monocyte?
found primarily in muscosal secretions,
including mucus, tears, saliva colostrum. what
1) Phagocytosis of invaders
immunoglobulin?
found in the nuclei of all infected cells. IgG 2) Present immunogens to T helper
antibodies to ____ develop slowly but can remain cells, the first step in an immune response
IgM
detectable throughout life. what antigen for EBV? 3) Release cytokines (monokines) that
IgG
affect other cells' activities
IgD
EBNA
IgA
read and skip
IgA
read and skip
has enzymes lysozomes which attacks and
destroys the cell wall of susceptible
fusion of phagosome, which results in the foramtion gives randomness to the receptor
bacteria, particularly gram positive
of the phagolysosome
bacteria
somatic rearrangement of TCT genes
degredation somatic arrangement of TCT genes
mucus
engulfment / digestion somatic rearrangement of TCR genes
tears, saliva
NADPH Oxidase somatic arrangement of TCR genes
acid
bile
degredation somatic rearrangement of TCR genes
tears, saliva
hla-b8
hla-dr2
hla-dr3
hla-dr4
--------------------
/Graves disease and type 1 diabetes
has recently been identified as the causative agent in help activate CD8 and CD4 cells. what cd /Rheumatoid arthritis, type 1 diabetes,
the majority of cases of what was previously known marker? and pemphigus vulgaris
as non-A, non-B hepatitis. is transmitted most /SLE, multiple sclerosis, Hashimoto
commonly by parenteral routes or through sexual CD3 disease, and myasthenia gravis
contact with infected persons. The majority of post- CD4 /Sjogren syndrome, myasthenia gravis,
transfusion non-A, non-B hepatitis cases are caused CD5 SLE, Graves disease, and type 1 diabetes
by CD6
hla-b8 - Graves disease and type 1
hepatitis C CD3 (Cluster Differentiation 3) diabetes
hla-dr2 - SLE, multiple sclerosis,
Hashimoto disease, and myasthenia
gravis
hla-dr3 - Sjogren syndrome, myasthenia
gravis, SLE, Graves disease, and type 1
diabetes
hla-dr4 - Rheumatoid arthritis, type 1
diabetes, and pemphigus vulgaris
/opsonization
/lysis of bacterial and maternal cells
/chemotaxis and leukocyte activation
-----------------------------------------------------
MATCH
/c5-c9 MAC
/covalently bonded fragments of c3 and c9
/c5a, c3a and c4a, anaphylatoxin leukocyte
receptors how many % of patients with
host is able to recognize a foreign antigen and rheumatoid arthritis are positive
build specific antigen-directed antibodies for RF. However, patients with chronic
responsible complement infections may also have RF.
activity competent
protein
immunocompetent 25%
covalently bonded competent and immunocompetent 50%
opsonization nota 75%
fragments of C3 and C9
100%
immunocompetent
chemotaxis 75%
C5a, C3a and C4a;
and
anaphylatoxin leukocyte
leukocyte
receptos
activation
lysis of
bacterial
c5-c9 MAC
and maternal
cells
how many J chain is needed for each IgM or IgA how many monomers linked together by a
molecule that is linked together? J chain and interchain disulfide bonds for
how many defenses does the body have?
IgM?
1
1
2
2 1
3
3 5
4
4 10
5 15
3
one five monomers
passive agglutination
reverse agglutination
forward agglutination
reverse passive agglutination
Th1
Th2
Th3
interaction of phagocytosis may be
Th4
infection and some tumores, against viral, only direct
Th1
recognize IgG antibody indirect
direct or indirect
th1 cells - a subset of T helper cells,
NK cells nota
that secrete cytokines that activate other
cells involved in the response
direct or indirect
th2 cells - release cytokines that are
required for B cell differentiation.
activate immune response
th1 and 2 - can promote the development
of cytotoxic cells believed to be develop
from Th0 cells
responses
Augmentation of Antibody
Enhancement of immunologic memory
==========================
C3 receptors on B cells and antigen-presenting cells
C3b and C4b bound to immune complexes and to
antigen
C3b and C4b bound to immune to complexes and to
is a cell that displays antigen complexed
antigen, C3 receptors on follicular dendritic cells
with major histocompatability complexes
on their surfaces
Responsible is a cell that displays antigen complexed with
Activity major histocompatability complexes on their
Complement Protein macropgahes
surfaces. this process is known as
viral cells
C3b and C4b bound to plasma cells
Augmentation of antigen presentation
immune complexes and Antigen presenting cell
Antibody
to antigen
Antigen presenting cell
C3 receptors on B cells
responses and antigen-presenting
cells
-CRP
is a multifunctional cytokine that
-haptoglobin
is a direct measure of light scattered by particles plays important roles in diverse
-fibrinogen
suspended in solution. cellular events such as cell survival,
-a1-antitrypsin
is more sensitive than turbidimetry. proliferation, differentiation, and
-ceruloplasmin
death
-a2-macroglobulin
-turbidimetry -interferon
-nephelometry -TNF
-a1-antitrypsin
-Fluid-phase precipitation -Interleukins
-precipitation reactions in agar gel
-CRP - concentration increases several
-rocket immunoelectrophoresis tissue necrosis factor
hundred times after injury
-Immunofixation electrophoresis
interferon - family of proteins
-haptoglobin - removes free hemoglobin from
Nephelometry produced rapidly by many cells in
circulation
response to viral infection
nephlometry - is a direct measure of light
-fibrinogen - is found in increased quantities
scattered by particles suspended in Interleukins - Some mediators that
at the site of an injury; it is converted to fibrin
solution. Nephelometry is more sensitive than act between leukocytes
to heal the injury
turbidimetry.
TNF - is a multifunctional
-a1-antitrypsin - is a family of serine protease
turbidimetry - measures cloudiness of solution. cytokine that plays important roles
inhibitors synthesized in the liver. Deficiency
is the measurement of light transmitted through a in diverse cellular events such as cell
causes premature loss of elasticity in the
suspension of particles survival, proliferation,
lung and liver damage
differentiation, and death
-ceruloplasmin
RPR
VDRL
FTA-ABS
TP-PA
-CRP
-haptoglobin
-fibrinogen
-a1-antitrypsin
-ceruloplasmin
-a2-macroglobulin
-fibrinogen
-ceruloplasmin
/c1 inhibitor
/anaphylatoxin inactivator
/MAC inhibitor
/complement type receptor type 1
MAC inhibitor
is important in enhancing phagocytosis and /c1 inhibitor - (C1INH) combines with Clr and is one of the ways that the body resists
CR3 is also important in these host defense Cls to block Cl activities. A deficiency in C1INH infection after microorganisms
mechanisms results in the syndrome hereditary angioedema, have penetrated the first line of defense
an autosomal dominant disease. The disease is
CR1 characterized by unregulated classical pathway Natural immunity
CR2 activation, resulting in vascular permeability passive immunity
CR3 and swollen mucous membranes in airways, artificial immunity
CR4 which can become blocked.
Natural immunity (inborn or innate
Complement receptor 1 (CR1) /anaphylatoxin inactivator - This resistance)
compound removes a single amino acid from
C4a, C3a, and C5a, rendering them useless as
anaphylatoxins.
HAI
dendritic cells
is the systemic form of type I hypersensitivity. It can langerhans cells
isolation of lymphocytes uses Density
be life threatening, causing shock or edema of the mast cells
gradient centrifugation with what?
upper respiratory tract
Dendritic cells
fluorescent
histamine
flow cytometry
anaphylaxis dendritic cells - is to process antigen material
ficoll-hypaque
prostaglandins and present it on the cells surface to the T-cells
light scattering
leukotrienes of the immune system
ficoll-hypaque
anaphylaxis langerhans cells - Dendritic cell found in the
dermis and squamous epithelia
alotype determinants
idiotype determinants
isotype determinants
it is to recognize the antigen
isotype determinants
B cell receptor
-allotypes - term used to describe unique kills miroorganims before enting the body
T cell receptor
differences within constant region of gamma
opsonin
and alpha heavy chain and kappa light chains Pus cells (neutrophils)
complement
present in different individuals
T cell receptor
-idiotypes - a result of the unique structures on
light and heavy chains individual
determinants characteristics of each antibody
Variation in the variable region
CA19-9
CA-125
CA15-3
AFP
B-HCG
CEA
AFP
lymphoid cells that has not been activated
CA19-9 - aids in diagnosing colon, gastric,
hepatobiliary, and pancreatic cancer.
lipids and nucleic acids are most immunogenic virgin cells
or weakly immunogenic? naive cells
CA-125 - Expressed in most
naked cells
nonmucinous epithelial ovarian tumors.
weakly immunogenic inactivated cells
CA15-3 - tumor marker for detection
naive cells
of breast cancer
Polyclonal Hypergammaglobulinemia
Monoclonal Hypergammaglobulinemia
waldenstrom macroglobulinemia
waldenstrom macroglobulinemia -
Uncontrolled proliferation of a clone of B cells
that synthesize a homogeneous IgM; cause
unknown
match the autoantibodies and associated
diseases.
Centromere
dsDNA
Histone
Nuclear RNP match the autoimmune disease to the
Scl-70 autoantibody present.
marked deficiency of all classes of Sjogren syndrome A (SSA [Ro])
immunoglobulins is detected after about 6 Sjogren syndrome B (SSB [LA]) pernicious aniema
months of age. B cells are markedly decreased or Sm chronic activate hepatitis
absent. what humoral immune deficiency? ============================== primary biliary cirrhosis
CREST (calcinosis, Raynaud syndrome, sle
-Bruton X-linked agammaglobulinemia esophageal sclerodactyly, and telangectasia) good pasture syndrom
-Hyper-IgM syndrome syndrome ============================
-Selective IgA deficiency hypomotility anti parietal cell antibody
-Ataxia-telangiectasia Found in SLE and low titers found in anti glomerular basement membrane, anti
rheumatoid arthritis and Sjogren syndrome alveolar basement membrane
Bruton X-linked agammaglobulinemia Drug-induced SLE anti-dsdna, anti-smith
SLE and mixed connective tissue disease anti-mitochondrial antibodies
-Bruton X-linked agammaglobulinemia Scleroderma (systemic sclerosis) anti-smooth muscle antibodies
- marked deficiency of all classes of Sjogren syndrome and SLE
immunoglobulins is detected after about 6 Sjogren syndrome and SLE anti parietal cell antibody - pernicious
months of age Diagnostic for SLE (high specificity) if present aniema
but low sensitivity anti glomerular basement membrane, anti
-Ataxia-telangiectasia - defect in a kinase
alveolar basement membrane - good
gene that regulates the cell cycle. The B and T
pasture syndrom
helper cells are affected.
anti-dsdna, anti-smith - sle
anti-mitochondrial antibodies - primary
-hyper-IgM syndrome = X-linked genetic
biliary cirrhosis
disease. what humoral immune deficiency
anti-smooth muscle antibodies - chronic
activate hepatitis
CA19-9
CA-125
CA15-3
AFP
B-HCG
CEA mechanism of a cell mediated-immune
defense whereby an effector cell of the
B-HCG immune system actively lyses a target cell
may account for the increased susceptibility of
older adults to infections, autoimmune disease
CA19-9 - aids in diagnosing colon, gastric, Antigen-dependent cell-mediated
and neoplasms
hepatobiliary, and pancreatic cancer. cytotoxicity (ADCC)
Antibody-dependent cell-mediated
-chronic autoimmune disease
CA-125 - Expressed in most cytotoxicity (ADCC)
-immune senescence
nonmucinous epithelial ovarian tumors. dependent cell-mediated cytotoxicity
-chronic leukocytopenia
(DCC)
CA15-3 - tumor marker for detection cell-mediated cytotoxicity (CC)
immune senescence
of breast cancer
Antibody-dependent cell-mediated
AFP - liver tumors, and germ cell tumors cytotoxicity (ADCC)
such as testicular cancer.
-opsonization
-anaphylatoxins
-immune adherence
-chemotaxis
chemotaxis
more common form of IgA subclass
Immune adherence - C3b adheres to
immune complexes and surfaces of
IgA1 more complex a molecule, the more
substances to facilitate clearing of these
IgA2 immunogenic it becomes. true or false?
molecules.
IgA3
IgA4 true
anaphylatoxins - C4a, C3a, and C5a
IgA2 cause basophils and mast cells to release
histamine and also cause smooth muscle
contraction and increased vascular
permeability.
chemotaxis - C5a is an anaphylatoxin
and induces the migration of neutrophils
and monocytes to the site
avidity
affinity
peptide bond
electrostatic bond
specificity
cross reactivity
occurs months to years after transplantation;
cross reactivity
mechanisms of rejection include both HMI and
CMI. type of graft rejection?
avidity - The affinity for multivalent
antigens and multiple antibodies to
acute rejection
combine; the extent of binding capacity.
hyperacute rejection occurs when an individual produces antibodies
This is greater than the cumulative
chronic rejection or a T cell response to his/her own antigens.
affinity constants for all antigenantibody
what disease?
pairs.
chronic rejection
T cell disease
affinity - The strength of the interaction
alloimmune disease
between a single antibody binding site
acute rejection - occurs within weeks of autoimmune disease
and a single epitope
transplantation. Rejection is due to CMI response weak immunity
electrostatic bond - Positively charged
hyperacute rejection - occurs within 24 hours of autoimmune disease
portions of one molecule are attracted to
transplantation.
negatively charged portions of another
molecule.This bonding is affected by the
chronic rejection - occurs months to years after
pH and ionic strength of the environment.
transplantation; mechanisms of rejection include
both HMI and CMI
specificity - refers to the antibody's
greatest affinity for a particular antigen.
process of phagocytosis
present on surfaces of naive B cells (monomers) produce cells of the immune system
initiation
IgM chemotaxis
bone marrow
IgM1 engulfment
thyroid
IgM2 degradation
throracic ducts
exocytosis
IgM3 lymphoid organs
read and skip
IgM1 lymphoid organs
read and skip
type I hypersensitivity
type II hypersensitivity
type III hypersensitivity
receptor of NK cells receptor of eosiniphils
type IV hypersensitivity
FcaR FcεR
type II hypersensitivity
FcbR FcyR
FcyR FcbR
type I hypersensitivity - reaction is classified as
FcεR FcaR
an immediate hypersensitivity reaction because
it occurs within minutes after reexposure to an
FcyR FcεR
allergen
FcεR - neutrophils FcyR - NK cells
type II hypersensitivity - reaction is due to IgG
or IgM antibodies directed against cell
surface antigens
avidity
affinity
peptide bond
electrostatic bond
specificity
cross reactivity
specificity
th1
th2
regonizes processed antigen associated with the th3 release the major basic protein and
MHC model th4 eosinophil cationic protein
-CRP
-haptoglobin
-fibrinogen
-a1-antitrypsin
-ceruloplasmin
-a2-macroglobulin
haptoglobin
responsible for allergies and
resets foreign substance and infuse
-CRP - concentration increases several hundred anaphylactic reactions. what
inflammation
times after injury immunoglobulin?
eosinophils
-haptoglobin - removes free hemoglobin from IgM
mast cells
circulation IgG
basophils
IgD
IgE
-fibrinogen - is found in increased quantities at IgE
the site of an injury; it is converted to fibrin to heal
basophils
the injury reaginic antibody (IgE)
-ceruloplasmin
Anti-DNAse B (AD-B)
ASO neutralization test
ASO rapid latex agglutination test
Streptozyme
culture
culture
/forbidden-clone theory
/clonal energy
/clonal selection
/polyclonal b cell activation
clonal selection
secondary response has a short latent phase of
/forbidden-clone theory - Burnet postulated how many days?
that when an error in self-recognition occurs during secretory IgA is a single or dimer held
fetal life and lymphocytes against an autoantigen 1-2 days together by a J chain?
are not destroyed, then autoantibodies are 3-5 days
produced. 5-7 days dimer
10-15 days
/clonal energy -Clones developed during fetal life single - serum IgA
are not stimulated by low doses of antigens. The 3-5 days dimer - secretory IgA
ability to produce antibodies against higher doses of
antigens is still present. 5-7 days latent phase
C3
C4andC3
C5, C6, andC7
C1 (q, r, s), C4, and C2
set of cell surface proteins for the acquired short lived circulating. very first cells that
============================
immune system to recognize foreign molecules migrate to site of infection
/Indicate collagen disease
/Increase risk for overwhelming infections
HLA basophil
/Increased risk for Neisseria meningitidis infection
MHC eosinophil
/Indicate consumption with classical pathway
LSA neutorphil
activation
CRP basophil
C3 - Increase risk for overwhelming infections
MHC Neutrophils
C4andC3 - Indicate consumption with classical
pathway activation
C5, C6, andC7 - Increased risk for Neisseria
meningitidis infection
C1 (q, r, s), C4, and C2 - Indicate collagen
disease
proteinase
protease
stages of t cell maturation stimulates hepatic cells to secrete CRP
properdin
(Opsonin). what interleukin number?
nbt
migration and proliferation
differentiation IL-1
properdin
selection IL-3
IL-6
proteinase - complement many of which
read and skip IL-9
are enzymes are called????
protease - proteins from the cleavage of
read and skip IL-6
a larger precurose by a
properdin - substances that stabilizes
the C3bBb complex
nbt - test used in order to confirm CBD in
patient
primary syphylis
secondary syphylis
latent stage syphilis
congenital syphilis
latent stage
syndrome is caused by infection during
substances used to break antibodies? pregnancy and can result in a wide spectrum of
primary syphylis - Inflammatory
birth defects. what rubella
lesions (chancres) appear 2 to 8 weeks.
2-mercaptoEthanol, DithioTreitol, 1% acectic acid
2-mercaptoEthanol, DithioTreitol r. fetusa
tertiary syphilis - characterized by
2-mercaptoEthanol rubellial meningitidis
granulomatous lesions known as
DithioTreitol congenital rubella
gummata. These lesions may develop in
late rubella
skin.
2-mercaptoEthanol, DithioTreitol
congenital rubella
latent stage syphilis - syphilis is
contagious and is generally considered to
begin after the second year of infection.
There are no clinical symptoms, although
serologic tests are still positive.
-allotypes proteinase
-idiotypes protease
-isotypes properdin
nbt
allotype
Nitro Blue Terazolium the IgG has how many subclasses?
-allotypes - term used to describe unique
differences within constant region of gamma proteinase - complement many of which are 4
and alpha heavy chain and kappa light enzymes are called????
chains present in different individuals protease - proteins from the cleavage of a
larger precurose by a
-idiotypes - a result of the unique structures on properdin - substances that stabilizes the
light and heavy chains individual determinants C3bBb complex
characteristics of each antibody nbt - test used in order to confirm CBD in
Variation in the variable region patient
the primary core of an antibody consists of the the t cell travels through the __ then __
the major humoral component is the
sequence of amino acid residues linked by of the thymus for differentiation
alloantibody
difsulfide bonds cortex , medulla
antigen
hydrogen bonds paracortex, medulla
antibody
peptide bonds cortex, paramedulla
autoantibody
cellular bonds nota
antibody
peptide bonds cortex , medulla
the three pathways converge at the point of cleavage ther term immunoglobulins has replaced
the three pathways converge at the point of
of ___ because not all antibodies have
gamma electrophoretic mobility
cleavage of C3 to C3b
C3 to C3b
cleavage of C4 to C3b
C4 to C3b macroglobulins
cleavage of C3 to C4b
C3 to C4b microglobulins
cleavage of C4 to C4b
C4 to C4b globulins
cleavage of C3 to C3b
C3 to C3b globulins
this granulocyte Has receptors for IgE and granules
this is the attraction between nonpolar groups. this is where many small b cells produce?
responsible for allergic reactions
hydrogen bonding -primary follicle of lymph nodes
basophil
hydrophobic bonding -secondary follicle of lymph nodes
eosinophil
affinity -lymph nodes
neutorphil
avidity -bone marrow
basophil
hydrophobic bonding -primary follicle of lymph nodes
basophil
isograft
three main physiologic activities of the allograft
this wbc Mediate IgE allergic response complement system xenograft
autograft
basophil host defense against infections
eosinophil interference between innate and adaptive allografts
neutorphil immunity
basophil disposal of waste allograft - tissue from a genetically
different member of the same
eosinophil skip and read species, such as a human kidney)
isograft - Transfer of tissue between
genetically identical individuals
autograft - Transfer of tissue from one
site to another within an individual
xenograft - Transfer of tissue between
two individuals of different species
CA19-9
CA-125
CA15-3
AFP
B-HCG
CEA
ca15-3
treatment for type I hypersensitivity?
CA19-9 - aids in diagnosing colon, gastric, two types of light chains
hypersensitization
hepatobiliary, and pancreatic cancer.
hyposensitization
alpha and beta
anti-inflammatory drugs
CA-125 - Expressed in most delta and gamma
opiates
nonmucinous epithelial ovarian tumors. episolon and mu
kappa and lambda
Patients can undergo immunotherapy
CA15-3 - tumor marker for detection
(hyposensitization), commonly referred to as
of breast cancer kappa and lambda
"allergy shots."
(anti-histamine, epinephrine -severe)
AFP - liver tumors, and germ cell tumors
such as testicular cancer.
DFA-TP
RPR
TP-PA
undigested part produced will be expressed on its MHA-TP usual activator in classical pathway of the
surface (known as ___) complement
microhemagglutination assay for T. pallidum
Fc (MHA-TP) complement
FAB cytokines
branch DFA-TP - A fluorescencelabeled antibody antigen or antibody
epitope or antigen (exocytosis) is used to detect T. pallidum in lesions. mannose
RPR - This test measures the antibody
epitope or antigen (exocytosis) (reagin) a patient has formed against antigen or antibody
cardiolipin, cholesterol, and lecithin. Tests are
read microscopically for flocculation
TP-PA - Treponemal antigen is combined
with liposomes. If antibodies are present, a
mat of agglutination forms in wells of a
microtiter plate
MHA-TP
TYPE I
TYPE II
TYPE III
what test which can detect antibodies in typhoid
TYPE IV
fever, tularemia, and brucellosis?
type IV
welix-felix test
widals test
type I hypersensitivity - reaction is classified what types of hypersensitivity reaction are
widals-felix test
as an immediate hypersensitivity reaction humoral mediated and immediate?
felix test
because it occurs within minutes after
reexposure to an allergen type I, IV
widals test
type II, III
type II hypersensitivity - reaction is due type I, II, III
widals - can detect antibodies in typhoid fever,
to IgG or IgM antibodies directed against type I, II, III, IV
tularemia, and brucellosis
cell surface antigens
type I, II and III
widal-felix test - which is an agglutination test
type III
based on the cross-reactivity of rickettsial
hypersensitivity - (immunecomplex)
antibodies with antibodies to the somatic “O”
reactions, immune complexes are
antigens of the OX-19 and OX-2 strains of Proteus
deposited on tissues, causing inflammation.
vulgaris and the OX-K strain of Proteus mirabilis
type IV hypersensitivity - reactions
are caused by soluble factors or
lymphokines released by T cells; antibody
and complement are not involved in this
reaction.
which body defense is adaptive
immunity?
which is an opsonin?
C3bBb
C4b2a which is more sensitive than IFA. The
which is faster and more convenient than the
c4a color intensity is proportional to amount
HAI for rubella testing
C3bBbC3b of Ab present for borrelia?
C4b2aC3b
-passive latex agglutination
EIA
-active latex agglutination
c4a IFA
-direct latex agglutination
ELISA
-indirect latex agglutination
C3bBb - C3 convertase of the alternative pathway EMIT
C4b2a - C3 convertase of the classical pathway
passive latex agglutination
c4a - opsonin ELISA
C3bBbC3b - C5 convertase of the alternative
Pathway
C4b2aC3b - C5 convertase of the classical pathway
who discovered phagocytosis and on what? who discovered the vaccine for polio?
who created a vaccine for human papilloma virus?
louis pasteur louis pasteur
ian frazer
edward jenner edward jenner
edward jenner
ernst haeckel ernst haeckel
louis pastuer
jonas salk jonas salk
ein gritzwald
paul erlich paul erlich
ian frazer
ernst haeckel, 1864 paul ehrlich
CAN BE ELLIE METCHNIKOFF
louis pasteur - 1880 - 1881 live, attenuated
louis pasteur - 1880 - 1881 live, attenuated louis pasteur - 1880 - 1881 live,
chicken, cholera and anthrax vaccines. 1885 -
chicken, cholera and anthrax vaccines. 1885 - attenuated chicken, cholera and anthrax
therapeutic vaccination; live attenuated vaccine for
therapeutic vaccination; live attenuated vaccine vaccines. 1885 - therapeutic vaccination;
rabies
for rabies live attenuated vaccine for rabies
edward jenner - smallpox vacination
edward jenner - smallpox vacination edward jenner - smallpox vacination
ernst haeckel - discovered phagocytosis
ernst haeckel - discovered phagocytosis ernst haeckel - discovered phagocytosis
jonas salk - antibody formation theory
jonas salk - antibody formation theory jonas salk - antibody formation theory
paul erlich - vaccine for polio
paul erlich - vaccine for polio paul erlich - vaccine for polio
ian frazer - human papilloma virus
ian frazer - human papilloma virus ian frazer - human papilloma virus