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Introduction in Infectious Diseases

Nino Badridze
MD, MPH, PhD
What is infection and Infectious disease
Definition

Infection:
is the invasion of an organism's body tissues by disease-
causing agents, their multiplication, and the reaction
of host tissues to the infectious agents and the toxins they
produce.

Infectious disease:
also known as transmissible disease or communicable
disease, is illness resulting from an infection.
Infectious Diseases as a Cause of Death
• Infectious diseases are responsible for a quarter to a third of all
deaths worldwide.

• Infectious diseases account for more than half of all deaths in


children under the age of 5.

• by the World Health Organization, of the top ten causes of death,


five are due to infectious diseases.

• The top single agent killers are: HIV/AIDS, malaria and


tuberculosis. The other top killers are lower respiratory infections
and diarrheal diseases.
Infectious Diseases

Definition of infection
 Complex process of interaction between pathogen
and human body
 Three factors are involved in the infection:
pathogen, host and environment
Factors Influencing Disease Transmission

Agent Environment
• Infectivity • Weather
• Pathogenicity • Housing
• Virulence • Geography
• Immunogenicity • Occupational setting
• Antigenic stability • Air quality
• Survival • Food

• Age
• Sex
Host •Behaviour
• Nutritional status
•Health status
Basic factors of infectious Disease

One of the factors of the infectious disease is microorganism.

Not all microbes have the ability to cause disease.

This feature - the cause of the disease is due to a special feature


of a part of microbes, which is called pathogenicity.

Pathogenicity This is the ability of a microorganism to invade a


susceptible organism, multiply and cause an infectious process.
Microbes Pathogenicity
Pathogenicity is a species characteristic of a microbe, which is
genetically polydeterminant.
Genetic polideterminant is caused because the gene is
responsible for the microbe - Capsule,
- Enzyme,
- Toxins
- and the production of other metabolic products.

According to pathogenicity, microbes are divided into 3


groups:

• Pathogenic,
• Conditionally-pathogenic
• non-pathogenic microbes
Pathogenic Microbes specificity

Pathogenic microorganisms are characterized by specificity, which


means that this or that pathogenic microbe entering the macro-
organism causes its characteristic

- Pathomorphological,
- Pathophysiological and
- Clinical changes,

Pathomorphological, pathophysiological and clinical changes are


determined by the state of the body's immune system at that
moment of agent invasion.
Microorganism pathogenicity
• Pathogenicity is determined by:
A) Virulence and
B) Toxicogenicity.
Virulence is the degree of microbial pathogenicity. It is an
individual variable sign of a microbe that characterizes only a
given strain.

Under different conditions virulence of the microbe can be weak


or highly.

Changes the pathogenicity of given strains of the microbe can


also altering virulence.
Microorganism pathogenicity
The pathogenicity of microbes is also determined by the
toxicogenicity of microbes.
Bacteria produce exo- and endo-toxins.

Bacterial cells release exotoxins into the environment.


Endotoxins are closely related to the structure of microbes and
are released only after their decomposition.

It has recently been discovered that exotoxins may also be


partially or completely related to the structural elements of the
microbe. Some bacteria produce both exotoxins and endotoxins
simultaneously
Exogenous infections
• Exogenous infections are mainly produced by gram-positive
microbes (diphtheria, tetanus, botulism, etc.).

• During an exogenous infection, there is only one foci (place) of


microbial multiplication in the body. Bacteria do not multiply in
different foci.

• Toxins have antigenic and immunogenic characteristics. Antitoxic


immunity is developed after the disease recovery.

• Exotoxic infections do not have recurrent and chronic forms.


Endogenous Infections
• Endogenous infections are produced predominantly by gram-
negative bacteria.
• Endogenous infections are characterized by bacteremia.

• Bacteremia is the process by which a microbe enters the


bloodstream from the invading foci, multiplies, followed by
the formation of secondary foci in various tissues and organs.

• Each newly formed hub can become a new source of


generalization.
Endogenous Infections
• Endogenous infections are less specific, they are not
characterized by organotropicity. They do not damage any
specific tissue and organ.
• Endogenous infections almost equally damage the tissues and
systems of the body.
• Clinical polymorphism is almost identically characteristic of
Endogenous infections.
• The endotoxin is weakly immunogenic.
• Endogenous infections are characterized by a waves, with
possible acute and chronic forms.
• According to pathogenicity, microbes are
divided into 3 groups:

• Pathogenic,
• Conditionally-pathogenic
• non-pathogenic microbes
Conditionally-pathogenic microorganisms
• Conditional pathogens can cause disease in people by direct
implementation to the tissue or in individuals with reduced
resistance to infection such as those who have an increased
use of antibiotics, the elderly, and newborn infants.
Conditional pathogens include Escherichia coli and
Streptococcus agalactiae.
Viruses, rickettsia, fungi, protozoa
and Helminths also are
characterized by Toxicity and other
virulence factors
Infectivity and it’s related factors
• Factors affect the pathogenicity of a microorganism are very
diverse.
• The infectious process is the result of a complex interaction of
these factors.
• In addition, the course and outcome of the infectivity are
influenced by the route of transmission of the pathogen, the
number of pathogens (dose, concentration) at the time of
infection, the gateway to the infection, and more.

• A microbe causes disease only when it enters the body in its


natural way. For example, the causes of typhoid and dysentery
enter the body through the digestive tract, and the flu, measles
viruses - from the mucous membranes of the respiratory tract,
and more.
Infectivity and it’s related factors
• The second major factor in the infectious process is the
macroorganism, which has a very complex non-specific and
specific mechanism of defense against microorganisms.

• Nonspecific protection factors include integrity of the skin and


mucous membranes, pH and enzymatic activity of the
stomach and intestines, normal microbial biocenosis,
lysozyme, phagocytosis and others.
• Chronic alcohol intoxication, trauma, fatigue and other
factors influences the body’s resistance to infections.
The immune system is a network of
biological processes
• The immune system is a network of biological processes that
protects an organism from diseases.
• It detects and responds to a wide variety of pathogens, from
viruses to parasitic worms, as well as cancer cells and objects
such as wood splinters, distinguishing them from the
organism's own healthy tissue.
The tasks of the immune system
• to fight disease-causing germs (pathogens) like bacteria,
viruses, parasites or fungi, and to remove them from the
body,
• to recognize and neutralize harmful substances from the
environment, and.
• to fight disease-causing changes in the body, such as cancer
cells.
Lymphocytes
• Lymphocytes are white blood cells that are also one of the
body's main types of immune cells. They are made in the
bone marrow and found in the blood and lymph tissue. The
immune system is a complex network of cells known as
immune cells that include lymphocytes.
Two types of Immune Response
• There are two types of immune response

A) Humoral immunity

B) Cellular immunity
Two types of Immune Response
• Humoral immunity is also called antibody-mediated immunity.
With assistance from helper T cells, B cells will differentiate into
plasma B cells that can produce antibodies against a specific
antigen.

• The humoral immune system deals with antigens from pathogens


that are freely circulating, or outside the infected cells.

• Cellular immunity is a protective immune process that involves the


activation of phagocytes, antigen-sensitized cytotoxic T cells and the
release of cytokines and chemokines in response to antigen
• T-lymphocytes, B-lymphocytes and
macrophages are involved in the body's
immune response.

• The course and outcome of the infectious


process depend on the quantity and
functional ability of T-lymphocytes, B-
lymphocytes and macrophages.
T lymphocytes
• T lymphocytes are part of the immune system and develop
from stem cells in the bone marrow. They help protect the
body from infection and may help fight cancer.
• There are 3 main types of T cells: cytotoxic, helper, and
regulatory. Each of them has a different role in the immune
response.
• B lymphocytes are part of the immune system and develop
from stem cells in the bone marrow. Also called B cell. B
lymphocytes
• B-cells fight bacteria and viruses by making Y-shaped proteins
called antibodies, which are specific to each pathogen and are
able to lock onto the surface of an invading cell and mark it
for destruction by other immune cells.
Types of B Lymphocytes

• Plasma Cell - allows to produce large quantities of antibodies


against specific antigens. They respond to signals from T cells
during infection and continue to produce antibodies until the
infection is controlled. Plasma cells are often found in chronic
inflammation.

• Memory B Lymphocyte - are long-lived cells that remain within


the body and allow a more rapid response to future infections

• T-independent B Lymphocyte - a small number can function


without T cell. They are particularly important for dealing with
encapsulated bacteria.
Antibodies produced during each infectious
disease are specific
Immunoglobulins
• The five primary classes of immunoglobulins are IgG, IgM,
IgA, IgD and IgE.
• These are distinguished by the type of heavy chain found in
the molecule.
• IgG molecules have heavy chains known as gamma-chains;
• IgMs have mu-chains;
• IgAs have alpha-chains;
• IgEs have epsilon-chains; and
• IgDs have delta-chains.
Immunoglobulin Classes
• IgM class - found in the early stages of the infectious process.
It accounts for 3-10% of human immunoglobulins.
• IgG class - Occurs two weeks after antigen exposure, more
often in viral as well as bacterial infections, it accounts for 70–
80% of immunoglobulins.
• IgA class antibodies are involved in the formation of local
immunity.
• IgE antibodies are involved in allergic reactions.
Environment –a 3rd main factor of infectivity

• Environmental conditions such as micro and macro


environment can affect the course and outcome of the
infectious process.

• Weather
• Housing
• Geography
• Occupational setting
• Air quality
• Food
Factors Influencing Disease Transmission

Agent Environment
• Infectivity • Weather
• Pathogenicity • Housing
• Virulence • Geography
• Immunogenicity • Occupational setting
• Antigenic stability • Air quality
• Survival • Food

• Age
• Sex
Host •Behaviour
• Nutritional status
•Health status
The Chain of Infection
• The Chain of infection is the way all infectious diseases spread.
• Each link has a unique role in the chain, and each can be
interrupted, or broken, through various means.
• The goal of infection prevention and control practice is to break
a link in the chain to prevent the transfer of microorganisms
Infectious Agent
• An infectious agent is a microorganism that is capable
infiltrating another living thing and producing infection.
Examples include bacteria, viruses, fungi and parasites.

• The invasion and multiplication of microorganisms, such as:


bacteria, viruses, fungi and parasites that are not normally
present within the body is an Infeqction
Classification of Infectious Agents

•Bacteria (cocci &bacilli)


Gram-negative or Gram- positive •Prion protein aggregates, lack
•Viruses: DNA or RNA nucleic acid)
•Viroid composed of single-
•Fungi stranded
-Disseminated or Localized •Plasmid is a extra chromosomal
double stranded small DNA
•Parasites molecule
-Protozoa
-Helminths
Bacterial Diseases

 Tuberculosis
 Scarlet Fever
 Tetanus
 Gonorrhea
 Diptheria
 Streptococcal Infections
 Pneumonia (can also be viral or fungal)
 Pertussis
 Bubonic Plague
Viral Diseases
*Common Cold
*Influenza
*HIV/AIDS
*Herpes (Simplex and Zoster)
*Hepatitis A,B,C, D, E, F and G.
*Measles, Mumps and Rubella.
*Poliomyelitis.
*Infectious mononucleosis.
Taxonomy Size Site of Propagation Examples

Disease
Prions 30–50 kD Intracellular Prion protein Creutzfeld-Jacob
disease
Viruses 20–300 nm Obligate intracellular Poliovirus Poliomyelitis

Obligate intracellular Chlamydia Trachoma, urethritis


trachomatis

Bacteria 0.2–15 μm Extracellular Streptococcus Pneumonia


pneumoniae
Facultative Mycobacterium Tuberculosis
intracellular tuberculosis
Extracellular Candida albicans Thrush
Fungi 2–200 μm Facultative Histoplasma Histoplasmosis
intracellular capsulatum

Extracellular Trypanosoma Sleeping sickness


gambiense
Protozoa 1–50 μm Facultative Trypanosoma cruzi Chagas disease
intracellular
Obligate intracellular Leishmania donovani Kala-azar
Extracellular Wuchereria bancrofti Filariasis
Helminths 3 mm–10 m
Reservoirs
• A reservoir is the place where an infectious agent can live. For
example, in or on humans, on objects and surfaces in the
environment, also animals, food, soil or water
Reservoirs of Infection agents

– Human Reservoirs: Infected individuals who may


or may not present disease. Carriers are infected
individuals without any signs or symptoms of disease
(AIDS, polio, HBV, HHV and etc).
– Animal Reservoirs: Zoonoses are diseases that
occur primarily in wild and domestic animals. About 150
different zoonoses are known (rabies, anthrax, and Lyme
disease).
– Nonliving Reservoirs: Two major sources are soil
and water.
• Soil: Clostridium tetani and botulinum.
• Water: Vibrio cholerae and Salmonella typhi.
The Ways of Transmission
Infectious Diseases
Ways of Transmission of Infectious Diseases

• Droplet contact: also known as the respiratory


route:
airborne disease.example: If an infected person coughs or sneezes
the microorganisms, suspended in droplets, may enter to body
through the nose, mouth or eye surfaces: ex: COVID 19
and etc ).
• Fecal-oral transmission: when foods or water become
contaminated (by people not washing hands). Common fecal-oral
transmitted pathogens include, hepatitis A, Vibrio cholerae,
rotaviruses, Entameba histolytica, Escherichia coli, and etc.
• Sexual transmission: sexually transmitted disease. Ex:
AIDS, Hepatitis B, hepatitis C and etc,
Ways of Transmission of Infectious Diseases
• Oral transmission:
Diseases that are transmitted primarily by direct oral contact such
as kissing, or by indirect contact such as by sharing a drinking
glass or a cigarette. Ex: Infectious mononucleosis (kissing
disease)

• By Blood transmission: blood-borne disease:


ex: Hepatitis C, Hepatitis B, HIV/ AIDS and etc.

• Vertical transmission:
from mother to embryo, fetus or baby during
pregnancy or labour. Ex: HIV/AIDS, Hepatitis B, Herpes
simplex and etc
Ways of Transmission of Infectious Diseases

• Iatrogenic transmission:
due to medical procedures: injection or
transplantation infected material.

• Vector-borne transmission:
transmitted by a vectors (which include mosquitoes,
ticks, and fleas). Vector is an organism that
does not cause disease itself but transmits infection from
one host to another. (Dengue fever, West
Nile Virus, Lyme disease, malaria).
Airborne

Droplet
Portal of Entry – “The Way In”
• The ‘Portal of Entry’ represents the ‘way in’- it is the way in
which an infectious agent gets in to the next host. The portal
of entry could include:

• Mouth or nose (droplets, contaminated food)

• Eyes (droplets, splashes)

• Cuts in the skin such as open wound or damaged skin, burns


or cuts, ulcers
Susceptible Host
• The ‘Susceptible Host’ represents the ‘Next Sick Person’. This
could include any person who is at risk of infection. A person’s
risk of infection can be impacted by their age and ability to
fight off illness. For example, babies and young children,
pregnant woman, older adults, people on certain types of
medication and people who are already sick or hospitalized
are at an increased risk for becoming infected.
The Chain of Infection- Review
Classification of Infectious Diseases

– Communicable Diseases:
– Spread from one host to another, directly or indirectly.
Example: Tuberculosis, herpes, flu, AIDS, chickenpox,
mumps, polio, hepatitis and others.

– Contagious Diseases:
– Spread easily from one person to another.
Example: Chickenpox, measles, Varicella and etc .
Classifying Infectious Diseases

• Subclinical Infection :
without significant sign and symptoms

•Opportunistic Infections :
caused by non-pathogenic low virulence microorganisms in
immunocompromised individuals (in people with weakened
immune systems, including people with HIV).
Opportunistic Pathogens

Opportunistic Pathogens: Organisms that normally do not cause


disease in their natural hosts in a healthy person. They may cause
disease if the host is weakened or if they enter a different part of the
body.

– Pneumocystis carinii pneumonia in AIDS patients.


– Neisseria meningitidis is usually harmless in respiratory tract,
but can cause meningitis.
– E. coli can cause urinary tract infections, meningitis,
pneumonia, and abscesses.
Classification of infectious diseases

By duration
 Acute − develops and runs its course quickly.
 Chronic − develops more slowly and is usually less severe, but
may persist for a long, indefinite period of time.
 Latent − A latent infection is hidden, inactive, or dormant.
characterized by periods of no symptoms between outbreaks of
illness.
Classification of infectious diseases

 By location
 Local − limited to a specific area of the body.
 Systemic − a generalized illness that infects most of the body
with pathogens distributed widely in tissues.
By timing
 Primary − initial infection in a previously healthy person.
 Secondary − infection that occurs in a person weakened by a
primary infection.
Emerging and re-emerging Infectious Diseases

• Emerging infections
are those that have recently appeared within a
population, increasing rapidly. (ex: HIV, SARS, Ebola,
COVID 19 and etc.).

• Re-emerging Infectious
Diseases whose incidence had significantly declined
in the past, but have again reappeared. (ex: tuberculosis
and etc.).
Relationships Between the Microbiota and the Host

SYMBIOSIS: “Living together”.

1. Commensalism: biological interaction in which one


species gain benefits while those other species are not
harmed

2. Mutualism: Both organisms benefit from living together


• E. coli synthesizes vitamin K and some B vitamins.
3. Parasitism: One organism benefits, the other is harmed
• Most disease causing bacteria.
Other Definitions

Bacteremia
Presence of small number of low virulence bacteria in the
bloodstream which do not multiply significantly e.g S. typhi,
E.coli

Septicemia
Presence of rapidly multiplying highly pathogenic
bacteria in the bloodstream. Septicemia can lead to;
• Sepsis
• Pyaemia
• Toxemia
Other Definitions
Sepsis;
A whole-body inflammatory state leading to multiple organ
failure and death resulting from sepsis-induced hypotension and
diffuse intravascular coagulation (DIC)
Pyaemia;
A diseased state in which pyogenic bacteria are circulating in the
blood, by development of abscesses in various organs.

Toxemia;
Blood poisoning by toxins from a local bacterial infection
Other Definitions
Viremia
Circulating viruses in the blood stream
Latent virus infection
Reactivation of infection from virus in latent phase
e.g. Herpes zoster: reactivation of Varicella Zoster Virus after
recovery from varicella

Oncogenic virus infection


virus which cause tumor e.g. HPV, HBV, HCV, EBV and ect,
Infectious diseases characteristic - epidemics and
pandemics

An epidemic
(from Greek ἐπί epi "upon or above" and δῆμος demos "people") is
the rapid spread of infectious disease to a large number of people in
a given population within a short period of time. An attack rate in
excess of 15 cases per 100,000 people for two consecutive weeks is
considered an epidemic.

A pandemic
(from Greek πᾶν pan "all" and δῆμος demos "people") is an epidemic
of disease that has spread across a large region; for instance multiple
continents, or even worldwide
Infections can be classified:
By anatomic location:
• Urinary tract infection
• Skin infection
• Respiratory tract infection
• GI system infections
• CNS infections: (encephalitis, meningitis, encephalomyelitis and
etc).
• Odontogenic infection (an infection that originates within
a tooth or in the closely surrounding tissues)
• Vaginal infections
• Intra-amniotic infection
• others
Periods (phases)
of Infectious Disease
Periods ( phases) of Infectious Disease

• Incubation period (Phase)


• Prodromal period (Phase)
• Period of illness (Phase)
• period of decline (Phase)
• Reconvalencence period (Phase)
The Stages of a Disease
Periods (stages or phases) of Infectious Disease
Periods (phases) of Infectious Disease

The incubation period: after the entry of the pathogen into the
host (patient). After entering the pathogen begins replication in the
host. However, there are insufficient numbers of pathogen to cause
signs and symptoms of disease.

Incubation periods can vary from a day or two in acute disease


to months or years in chronic disease. Factors involved about the
length of the incubation period are varous, and can include strength
of the pathogen, strength of the host immune defenses, site of
infection, type of infection, pathogen dose and etc.

During this incubation period, the patient is unaware that a disease is


beginning to develop.(the patient is asymptomatic)
Periods ( phases) of Infectious Disease

The prodromal period

The prodromal period occurs after incubation period.


During this phase, the pathogen continues to multiply and
the host begins to experience general signs and symptoms
of illness(not specific), which typically result from
activation of immune system, such as fever, pain, sore
throat, swelling, or inflammation.

Usually, such signs and symptoms are too general (not


specific) to indicate a particular disease.
Periods (phases) of Infectious Disease

Period of illness (Phase)

All specific clinical symptoms characteristic of this


particular disease will be revealed at this time.
This period is characterized by great diversity

During these period the signs and symptoms of disease are


most obvious and severe.
Periods (phases) of Infectious Disease

Period of decline

The period of illness is followed by the period of decline, during


which the number of pathogen particles begins to decrease, and the
signs and symptoms of illness begin to decline.

However, during the decline period, patients may become susceptible


to developing secondary infections because their immune systems
have been weakened by the primary infection.
Periods (phases) of Infectious Disease

Reconvalencence period (Phase)

The final period is known as the period of convalescence.

During this stage, the patient generally returns to normal


functions, although some diseases may cause permanent
damage and the body cannot fully repair.
Diagnosis
of Infectious Diseases
Diagnosis
of Infectious Diseases
• Is based on complex methods which includes collection of
anamnesis, patient's complaint, laboratory and instructional
examinations.

• collection of epidemiological data is of great importance in


the diagnosis of infectious diseases. Epidemiological data
gives us possibility to determine the source of infection, the
mechanism of infection and the conditions.
Diagnosis
of Infectious Diseases
• Examination of the skin and mucous membranes is also very
important.
• During the course of this or that disease, rashes of different
nature appear on the skin - exanthema (roseola, petechiae,
papules, vesicles, pustules.
• Because of it is essential to look to
• Mucous membranes,
• Conjunctiva, mouth,
• other
Diagnosis
of Infectious Diseases
In order to describe the objective condition of the
patient, it is necessary to use all research methods
according to organs and systems, such as:

• Palpation,
• Percussion,
• Auscultation
Diagnosis
of Infectious Diseases
An important role in the diagnosis of infectious diseases plays

A) nonspecific (blood, urine analysis, biochemical


examinations, etc.), as well

B) specific laboratory methods (microscopic, bacteriological,


virological and serological),

which can be used to determine the cause of the disease.


Laboratory Diagnosis of Infectious Diseases
STAINING

Gram’s stain differentiates between organisms with


thick peptidoglycan cell walls (gram-positive) and
those with thin peptidoglycan cell walls and outer
membranes that can be dissolved with alcohol or
acetone (gram-negative).

The examination of CSF and joint, pleural, or


peritoneal fluid with Gram’s stain is useful for
determining whether bacteria are present.
ELISA
The enzyme-linked immunosorbent assay (ELISA) is a test
that uses antibodies or antigen to identify a substance.

Antigens from the sample are attached to


a surface. Then, a further specific
antibody is applied over the surface so it
can bind to the antigen. This antibody is
linked to an enzyme, and, in the final step,
a substance containing the
enzyme's substrate is added. The
subsequent reaction produces a detectable
signal, most commonly a color change in
Laboratory Diagnosis of Infectious Diseases

Immunofluorescent stains

The direct immunofluorescent antibody technique uses


antibody bound to a fluorescent compound (e.g.,
fluorescein) and directed at a specific antigenic target to
visualize organisms

Evaluation under microscope


DETECTION OF PATHOGENIC AGENTS BY CULTURE

To culture bacterial, fungal, or viral pathogens.

An appropriate sample must be placed into the proper


medium for growth (amplification).
ISOLATION OF VIRAL AGENTS

Virus may be detected by direct observation of the cultured cells for


cytopathic effects or by immunofluorescent detection of viral
antigens after incubation

Conventional viral culture is useful for detection of rapidly


propagated agents, such as herpes simplex virus.

Viruses that grow more slowly (e.g., cytomegalovirus and varicella-


zoster virus) can be detected quickly by shell-vial culture, in which
the specimen is centrifuged on a monolayer of cells that is then
incubated for 1–2 days and finally is stained for viral antigens with
fluorochrome-conjugated antibodies.
NUCLEIC ACID TESTS (NAT test)

Using PCR technology (polymerase chain reaction)

For detection of genetic materials (DNA or RNA) of pathogen


( Gold standard)

Nucleic acid tests (NAT) are used for four purposes.


 First: to detect, and sometimes to quantify, pathogens;
 Second: for identification of organisms, that are difficult to
identify by conventional methods;
 Third: to determine whether two or more isolates of the same
pathogen are closely related (belonging to the same “clone” or
“strain”);
 Fourth: to predict the sensitivity of organisms (typically viruses)
to chemotherapeutic agents.
Prevention of
Infectious diseases
Prevention of Infectious diseases

Immunization Principles and Vaccine Use

• Immunization is very important for economic savings, and


Patients quality of life.

• Since childhood vaccines have become widely available in


the United States, major declines in rates of vaccine-
preventable diseases among both children and adults have
become evident
Prevention of Infectious diseases
Immunization

Active - using Vaccine


Passive - Immunoglobulin
Active Immunity

• Protection produced by the person's own


immune system
• Usually permanent
Principles of Vaccination

General Rule

The more similar a vaccine is to the


disease-causing pathogen of the organism,
the better the immune response to the
vaccine.
Classification of Vaccines
Vaccine types
Commercially available vaccines classified into four types:

• Live-attenuated vaccines
• Inactivated vaccines (killed)
• Subunit, recombinant, polysaccharide, and
conjugate vaccines
• Toxoid vaccines
Live-attenuated vaccines
Live vaccines use a weakened (or attenuated) form of the pathogen
(germ).

Live vaccines create a strong and long-lasting immune


response.

Just 1 or 2 doses of most live vaccines can give lifetime protection

Examples of Live vaccines:

• Measles, Mumps, Rubella (MMR combined vaccine)


• Rotavirus
• Smallpox
• Chickenpox
• Yellow Fever

Inactivated (killed) vaccines
Inactivated vaccines use the killed version of the Pathogen(germ)

Inactivated vaccines usually don’t provide immunity (protection)


that’s as strong as live vaccines.

So we need several doses over time (booster shots) in order to


get ongoing immunity against diseases.

Inactivated vaccines:

• Hepatitis A
• Flu
• Polio
• Rabies
Subunit, recombinant, polysaccharide, conjugate vaccines
Subunit, recombinant, polysaccharide, and conjugate vaccines use
specific pieces of the germ — like its protein(antigen) or capsid.

They can also be used on almost everyone who needs them,


including people with weakened immune systems.

One limitation of these vaccines is that you may need booster shots
These vaccines are used to protect against:

• Hib (Haemophilus influenza type b) disease


• Hepatiti B
• HPV (Human papilloma virus)
• Whooping cough (part of the DTaP combined vaccine)
• Pneumococcal disease
• Meningococcal disease
• Shingles
Toxoid vaccines
Toxoid vaccines use a toxin (inactivated) made by the germ
that causes a disease.

They create immunity to the parts of the germ that cause a


disease instead of the germ itself.

Like some other types of vaccines, toxoid vaccine need


booster shots to get ongoing protection against diseases.
Toxoid vaccines are used to protect against:

• Diphtheria
• Tetanus
Passive immunity
• Passive immunity is the transfer of active humoral
immunity of ready-made antibodies.

• Passive immunity can occur naturally, when


maternal antibodies are transferred to the fetus through
the placenta.

• and it can also be induced artificially, when high


levels of antibodies specific to pathogen or toxin
(obtained from animals, humans, horses) are
transferred to non-immune persons through blood
products that contain antibodies, such as in
immunoglobulin therapy or antiserum therapy.
Passive Immunity
• Temporary protection that diminishes with time
(weeks, months)

• Passive immunization is used when there is a high risk


of infection and insufficient time to develop its own
immune response.
• Passive immunization can be provided when people
cannot synthesize antibodies, and when they have been
exposed to a disease that they do not have immunity.
Examples:

Hepatitis B (HBV)

Hepatitis C (HCV)
Examples:
Prevention

Hepatitis B (HBV)
HBV vaccine and HBIG

Hepatitis C (HCV)
No prophylaxis exists
Treatment of Infectious
diseases

Antimicrobial therapy
Treatment of Infectious
diseases

Antibacterial therapy
Antiviral therapy
Antiprotozoal therapy
Antifungal therapy
Treatment of Bacterial Infections
• Antibacterial agents (antibiotics), like all antimicrobial
drugs, are directed against unique targets of the bacteria
cell
• Bactericidal antibiotics kill the bacteria that are within
their spectrum of activity;
• Bacteriostatic drugs only inhibit bacterial growth.

• While bacteriostatic activity is adequate for the treatment of


most infections, bactericidal activity may be necessary for cure
in patients with altered immune systems (e.g., neutropenia),
protected infectious foci (e.g., endocarditis or meningitis), or
specific infections (e.g., complicated Staphylococcus aureus
bacteremia).
Antiviral therapy

• Interferons
• DAA
• Other
Antiviral therapy

• Interferons
 Conventional
 Pegylated
Antiviral therapy

(DAA)

Direct-acting antivirals (DAAs), are drugs


targeted at specific steps within the viral life
cycle and results in disruption of viral
replication and infection
Antiviral therapy
DAA and target proteins
• Tenofovir (reverse transcriptase)
• Entecavir (reverse transcriptase)
• Sofosbuvir (NS5B)
• Ledipasvir (NS5A)
• Velpatasvir (NS5A)
• Dolutegravir (integrase)
• Raltegravir (integrase)
• Lopinavir (protease)
• Lamivudin (reverse transcriptase)
• etc
Elimination, and Eradication of infection

• Elimination: requiring the reduction to zero of new


cases in a defined geographic area.
sometimes defined as reduction in the local sustained
transmission of an infection in a geographic area.

• Eradication: Absence of a disease is achieved and its


absence can be sustained without ongoing
interventions. The only vaccine reventable disease that
has been globally eradicated thus far is smallpox.
Thanks for
your attention

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