M.A.R.C.

Inc.
Carlsbad, CA

Judy A. Mikovits, PhD

April 27, 2019

www.plaguethebook.com
jamikovits@gmail.com
marcinc137@protonmail.com
805-797-6967
 The$Politics$of$AIDS$and$HIV
Political Influence on Scientific Research and the Impact it has on us ALL

HIV -1 Isolation- 1982

MANY DEATHS BEFORE ESTABLISHMENT

November 7,1991 BELIEVED IN RETROVIRAL CAUSE
 September 11. 2010

Why? Because in 1991 ONE million Americans were Infected with HIV
in 2010 when studies showed between 10-25 Million Americans were infected with XMRVs
THE BLOOD Supply IS CONTAMINATED with MLV-related viruses!
Summary/Conclusions
NYAS Mikovits March29,2011
! Data1suggest1there1are1different1strains1of1Gamma1
Retroviruses1that1can1infect1humans
! Assays1that1capture1the1variation1of1these1viruses1in1the1
blood1supply1are1the1best1i.e.1Serology1and1transmission
! Cerus Technologies1can1inactivate1infectious1strains1of1
XMRV/HGRVs1in1Blood1Components
! New1Disease1associations1include1leukemia,1lymphoma1
and1the1platelet/megakaryocyte11disorder,1ITP
! Need1more1full1length1sequencing!!!1

FDA Approval December 1 2014 of Intercept Blood System 30

 she said.related came to methods of testing XMRVs and variants
gift-wrapped with hundreds Nevada, of eager
andinthe main champion of the idea in Science that showed entire sequences of the data,” Blomberg says.
blood. Abbott Laboratories has filed patent applications that XMRV and its relatives play a role in XMRV and infection of fresh cells, Mikovits Two other presentations offered some

“ Science relating started this and Science is going to End This”

CFS. Her opponent, an erstwhile supporter, revealed only partial viral sequences that she support for gammaretroviruses in CFS
initially researchers.”
to detection of XMRV by use of immunoassays
was heavyweight retrovirologist patients, but both detected just
John Coffin of the Tufts Univer- antibodies and not the virus
s a won- Nancy Klimas, a CFS clinician hasatfiled the patentUni-

www.sciencemag.org on April 30, 2013

sity Sackler School of Graduate itself. One study, led by Kenny
and molecular-based
John Coffin to Frank Ruscetti assays. Gen-Probe
November 2010 Biomedical Sciences in Boston. De Meirleir of Vrije Universit-
hree
EPORTS legsapplicationsversity of Miami in Florida,
relating to the assays they performed stressed thethat
stage at the
When Mikovits and Coffin took
in
the meeting, which
NEWS&ANALYSIS
eit in Brussels, had WPI run its
assays. When asked whether
was organized by IACFS/ the new findings invalidated
om CFSthis paper. Blood Working Group had analyzedME samples
Failure to Confirm XMRV/MLVs in the
(an international We report here the results of a comprehen-
associa- his data, De Meirleir said,
V I R O LO G Y
tion devoted to the sivedisease)
study in which multiple laboratories analyzed “I’m not goingfortothe say yes Working
Blood or
had used from just 15 people who had testedandpositive and attracted 460
patients, they the
researchers
sat onsame The blood samples for XMRV/P-MLV.
Waning Confl ict Over XMRV
no.” The other report
works at came
the Blood Sy

Blood out offorPatients

Supporting Online Material with Chronic in earlierFatigue
oppo- from Maureen tute Hanson,
in San a plant
Francisco, C
luck gammaretroviruses reports. “IThese
site sides of the lectern.
persons who
ing their introductions,
blood samples, which were drawn from
Dur-
Coffi And Chronic
n were previously reportedFatigue
to be XMRV- Syndrome
geneticist at Cornell
sity, who collaborated
Univer-about he
was “dubious”
with
can be aerosolized. V
www.sciencemag.org/cgi/content/full/science.1213841/DC1
it,Syndrome:
found wouldAbeMulti-Laboratory
much more confident Study putting
clasped his hands
these
mouth, looking
in front of his
(2) or P-MLV–positive (4) and from blood donors
like a man in Less than a day after a had asserted—explained the XMRV
OTTAWA, CANADA—
Pro and
CFS
the XMRV
clinicians.
DNA it sequences
con. Judy Mikovits (left) argued for the link between human gammaretro-
“Even
Knox of though
the Wisconsin
may besaid Mik
in Milwaukee
prayer who wishedwho this previously tested negativemanyfor XMRV, werefound in some patient samples. wrong, it’s still ing.”
Materials and Methods would
aliquoted
new study
intotoreplicate
dealt what
tubes and
viruses and CFS, and John Coffin countered.
consider
assembled
a lethal
into In Ottawa, Mikovits came out
certainly
Knox, possi-
who once c
the
Grahamiso-Simmons, putative 1
Simone A. Glynn, retroviruses 2
Anthony L. Komaroff, toJudy
rest if I had
A. Mikovits, 3 a Tobler,
Leslie other
H. larger,
all stop. Neither addressed
4
the
blow 1 the controversial theory that a newly ble that
swing-there’s had
a virus
a in these with t
falling-out
SOM Text 5 5 6
John Hackett Jr., Ning Tang, William M. Switzer, Walid Heneine, Indira K. Hewlett, The controversy 6
by name, andcoded
7
panels
they avoided eyetogether
detected contact.
virus, XMRV, with replicates
said were from to
is linked the of exper-and
XMRV
chronic ing.MLV family
But she didn’t patients
make thethatcaseweforneedXMRVto identify,”
, “thisshe said.
is obfuscating wha

experi-
Tables
Jiangqin Zhao,S1
more
to
7
S10
Shyh-Ching
powerful 8 study,” 9Klimas said.
Lo, Harvey J. Alter, Jeffrey M. Linnen, Kui Gao, John M. Coffin, 10
Mikovits Sim-
and 10
colleagues
began shortly
fatigue
published
testing8 was
11
skeptics aof
performed
after
syndrome
paper
the
known
(CFS),
imentally prepared positive control samples. The
team,
theory
as
which
squared
gammaretroviruses.
proponents
includes
off in a
and
Francis
meet-
She
which said
stands
Ruscetti of
virus–related
her
for
the
Cort
xenotropic
patients
virus. Instead,
Johnson,
murine
have
she held
a CFS
leukemia
fast
offered to
new
advocate,
XMRV
to be
gistfor
says
at good
the
many
obvious.”
rea-
Jonas
University
B
o
12 12 4 (http://scim.ag/mikovits)
13 October
ing here.
14 2009 in fully blindedCancer
U.S. National so as Institute
to re-evidence
in Frederick,
that people son.with
“It wasCFSas if(known
the medicalas gods, afterKnox
who like yearshas faile
Mary F. Kearney, Francis W. Ruscetti, Max A. Pfost, James Bethel, Steven Kleinman,
cked
Jerry
out mons
References
A. Holmberg, (23–35)
agrees that a larger study would
15 1
Science that
Michael P. Busch, * for the Blood XMRV Scientific ResearchXMRV, a mouse retrovirus,
have mademove bias. link
the startling
laboratories
and
These
In
using
CFS
director
between
one
(23
samples
corner
at highly
Sep-
was were
Maryland,
Judy
sensitive
suggest
the Whittemore
tested
these
also had
Mikovits,
and
Peterson
bypreliminary
research
previously
ninemyalgic
gammaretroviruses
Institute had amay
data that of neglect,
encephalomyelitis
virustravel
“highly apology
related” to
had bent
in some
in XMRV
down and
countries)
the form . of a simple
ownoffered
studies
answer
handle”
upofanCFS pat
that
Mikovits’s mo
Working
To claim Group (SRWG)†
Appendix more S1 power, but he says the 15-person study Nevada,
tember, p. 1694). validated
But the finding,
for heralded
Neuro-Immune through
Disease
nucleic acid, serological, and culturethe air.
(WPI) “That’s
in pretty
Reno, scary,” she
Unlike said.
the came
original gift-wrapped
study that with
appeared hundreds
like the of eager
argument follo
by many patients as the long-sought cause
and the of mainCoffi n beganofby
champion thestressing
idea in that he initially
Science researchers.”
that showed entire sequences of the data,” Blomberg say
assays
their baffling disease, soon met (tables
thata XMRV S1 toand
barrage of S5)its for XMRV
thought the play
relatives XMRV-CFSaandroleother
intheoryXMRV“wasand
a won-infection ofNancy
freshKlimas, a CFS clinician
cells, Mikovits Twoat the Uni-present
other
’reMurine
going is enough
leukemia viruses (MLVs), including“to make conclusions
xenotropic-MLV–related virus (XMRV), haveabout
been
criticism as labthe MLVs
after (16).
lab failed The
Her two
to replicate
CFS. it. laboratories
opponent, derful that
hypothesis.”
an erstwhile had
But itpre-
supporter, rested on three
revealed onlylegs versity
partial viral of Miami in
sequences Florida,
that she stressed
supportthat forthe
gammar
12
equence September
controversially linked to
assays 2011;
chronic fatigue
being accepted
syndrome
totally 20
(CFS). To September
explore this
unreliable.”
issue in
we compiled coded replicate samples of blood from 15 subjects previously reported to be
2011
greater
Results
depth,
The new study
of a
viously
(http://scim.ag/xmrv-cfs)
published
on
found
wasby
22
John
an
heavyweightassociation
Science
September
Coffi n of the patients,
Tufts
CFS participated in this study (2, 4). All nine
for
of a stool.
retrovirologist the
AfterMLVs
Mikovits
Univer-
removing
and
with blood from CFS Blood Working Group had analyzed samples
co-workers had used from just 15 people who had tested positive
patients,
antibodi

Published larger
XMRV/MLV–positive online 22
(14 with CFS) andSeptember
study 2011;
from 15 healthy donors
of in150 CFS previously determined to be
patients
and presented at the conference
timenegative
are expected convincinglylaboratories
sity for
used
the fiSchool
Sackler rst the
XMRV/P-MLV
polymerase chain reaction to pluck out for gammaretroviruses in earlier reports. “I
of Graduate
from thenucleic
virus andacid
itself. On

CREDIT: JON COHEN

showed that not
Biomedical oneSciences
of DNA in Boston. sequence it, found would be much more confident putting these De Meir

ncemag.org on April 30, 2013

for the viruses. These samples were distributed a blinded fashion to nine laboratories, which amplification testing find(NAT), Coffinserological, and/or
10.1126/science.1213841
nine labs, including WPI, could When reliably
Mikovits andantibodies tookto XMRV, and shown that the iso- putative retroviruses to rest if I had a larger, eit in Bru
performed assays designed to detect XMRV/MLV nucleic acid, virus replication, and antibody. XMRVOnly or its closeculture
relativesassays
known
the stage ofmurine
as their
at own choosing,
lated
the meeting, virus
whichcould which infectwere
cells in lab experi- more powerful study,” Klimas said. Sim- assays.
whelmed early next year.
two laboratories reported evidence of XMRV/MLVs; however, replicate sample results showed leukemia viruses (MLVs) in was
people organized
who pre- by
incorporated into parallel or serial testing algo-IACFS/
ments. All the legs have now been kicked out mons agrees that a larger study would havethe new
viously had tested positive forME them. (an international associa-
for both XMRV and MLVs, he said. “To claim more power, but he says the 15-person study his data
disagreement, and reactivity was similar among CFS subjects and negative controls. These Both results rithms intion
n order to generate final results.
than one The
“With- Mikovits said she hopes to
indicate that current assays do not reproducibly detect XMRV/MLV in blood samples andthe
havethat
full
Mikovits
co-authors of the
and Coffi
majority
paper by of
and
weredevoted
among
laboratories
the
to the
so-called460included
attracted
thatdisease)
there’s more
have toassays
researchers
to show a to
XMRV, you’re going is enough “to make conclusions about the
detect
virus that has a sequence assays being totally unreliable.” Results of no.”
“I’m no
a Th
bloodsaid
ge,” donor screening is not warranted.of her new viruses “in a couple of
sequences Blood Working mouse DNA contamination either on all samples
Group. At and
the patients,
same time, they sat on
that’s oppo-
different from XMRV ,” he said. larger study of 150 CFS patients are expected from Ma

CREDIT: JON COHEN

Science also ran aor partial site sides(http://
retraction of the lectern. Dur- presentation underwhelmed early next year.
Mikovits’s genetici
on all NAT-positive samples.

Pare
scim.ag/R-H-S) of the October ing 2009
their introductions,
paper several Coffi
of nthe scientists attending. “With- Mikovits said she hopes to have full sity, wh
the data weeks.”
reviously unknown murine leukemia virus ma (2, 3). In an independent study, –JON other patients
afterCOHEN Fourteen
one of WPI’s collaborators clasped patients
his handswith
discov- inout CFS,
front
the of togetherit’swith
hissequence,
full hard to judge,” said sequences of her new viruses “in a couple of CFS clin
differentially regulated posttranscriptionally.
(MLV)–like sequences were identified in, with CFS were reported to harbor MLV-related
and implicated as a potential infectious virus sequences, but not XMRV, in PBMC and
one person
ered that a contaminant—as reporting
mouth,
many criticscontact
looking like
(17)—allprayer
of whom
with
a man
Graham
who wished
in a CFS who
Simmons,
were this
previously
patient
reported
would viruses
presented the data weeks.” the XMR
Pro and con. Judy Mikovits (left) argued for the link between human gammaretro-
toand John Coffin countered.
and CFS,
–JON COHEN
wrong, i

Using a more sensitive 3′ rapid amplification of

cause of, human prostate cancer in 2006 (1).
These sequences appeared to be closely related
plasma (4). These sequences were derived from
1810
viruses resembling polytropic MLVs (P-MLVs)
all stop.
30 Neither addressed
SEPTEMBER 2011the VOL 333 SCIENCE www.sciencemag.org
be XMRV/P-MLV–positive by at least one meth-
other by name, and they avoided eye
od (table S6)—were enrolledbegan
into the
contact.
studyafter
Published atAAAS
by
said were from the XMRV and MLV family
twoknown as gammaretroviruses. She said her
ble that t
patients that we need to
www.sciencemag.org The controversy shortly Cort Johnson, a CF
 Solution for Agency Heads for 2009 and 2010 XMRV Publications in Elite Journals? ?
Plague of Corruption

In 2011 Harvey Alter picked the poison to have this 2010 confirmatory study withdrawn
Contamination of the Blood Supply, Additional Strains, Disease Associations
Infection in the Worldwide
XMRV/MRVs'Detection'in'Cancer'&'Blood'Diseases'in'
addition'to'Prostate'Cancer'and'CFS
ID# XMRV( Cancer/blood(
status disease
1103 positive MCL XMRV%in%Families%of%CFS%Patients%
1109 positive Thymoma
1118 positive myelodysplasia
1125 positive MCL n.t. n.t.

1186 positive Lymphoma

Lymphoma
1199 positive Lymphoma
1150 positive Lymphoma
3818 positive MCL n.t.

1174 positive Thymoma Ab+ V+,%Ab+ CFS

1205 positive lymphoma
1172 positive MCL
3848 positive ITP
n.t. n.t. n.t.
3827 positive ITP n.t.

1113 positive CLL CFS$(12) Ab+ Lymphoma$

1322 Not'tested MCL
V+,%Ab+
1181 positive CLL
1188 positive CLL
1189 positive MCL
3814 positive ITP
 21st Century Acquired Endocannabinoid Immune Dysfunction:
Unintended? Consequences of Unsafe Vaccinations & CDC Schedule

Diabetes
Cardiovascular Disease*
Neuroendocrine tumors*
Psychosis

“One of the most widely distributed biological products that frequently involved mice or mouse tissue, at least up to recent years,
are vaccines, especially vaccines against viruses . . .
It is possible that XMRV particles were present in virus stocks cultured in mice or mouse cells for vaccine production,
and that the virus was transferred to the human population by vaccination
Frontiers in Microbiology published January 2011
“Before Litigation There was Truth”
Mike Hugo
 Given Protection from Liability by 1986 National Childhood Vaccine Injury Act:
Federal Agencies, Pharmaceutical Companies, Mainstream media and Scientific Journals
Collude to Censor Truth
Vaccine Whistleblower: Exposing Autism Research Fraud at the C…aley, Robert F. Kennedy Jr.: 9781634509954: Amazon.com: Books 10/14/15, 7:14 AM

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 “That doesn’t mean there isn’t another gammaretrovirus to
be found. I think enough evidence has been presented that
maybe another infectious retrovirus is there. These studies
will continue to go on, looking for MLV-related viruses.”
John Coffin NIH State of the Knowledge Workshop on ME/CFS from April, 2011

Taken together these data suggest there are

additional human gamma retroviruses which may be involved in the
Pathogenesis of neuroimmune disease and cancer!

“The question, which urgently needs to be answered is whether the

plague feared by Coffin and Stoye has already arrived, but we do not
Recognize it…
THEY SEE WHAT THEY WANT TO SEE AND THAT’S THE REAL PLAGUE”
Plague Chapter 21 p382
Residual DNA/RNA deriving from cultured cells - Total amount of DNA: 1.7-3.7 µg/dose,
the 80% of which was human (Human fetal DNA / RNA from the MRC-5 cell line). Other amount of DNA: chicken

Adventitious viruses - Human endogenous retrovirus K, Equine infectious anemia virus, Avian leukosis virus, HERV-H/env62
Other microbial contaminants - Proteobacteria, nematode-helminth

Human endogenous retrovirus K - 32 sequences

Equine infectious anemia virus - 2 sequences
Avian leukosis virus - 2 sequences
HERV-H/env62 - 4 sequences
These viruses are known to be adventitious vaccine contaminants and are known to ​be potentially dangerous, which is
why manufacturers are required to verify that they are completely absent from the vaccine.
It follows that this in-depth analysis in this vaccine confirms two nonconformities on efficacy and safety:
The presence of rubella in a very low number of copies (subthreshold)
The presence of potentially dangerous adventitious viruses ​which certifies that there is no adequate control on vaccines
because if there were, these elements would have been detected.
The Name Game and the Immaculate Recombination
How many have we created, John? How many retroviruses are out there Judy
Mikovits asking a question to Dr. John Coffin
at the Ottawa IACFS ME/CFS meeting 23 September 2011
Plague Chap 17 p 284
 "However, the group also recommended that further studies be undertaken
urgently and
internationally to put into perspective the very low levels of RT activity found
4.1. Initial findings
The discovery in 1995 of reverse transcriptase (RT) in the vaccines."
activity in marketed measles, mumps and rubella
(MMR) vaccine raised concerns that the vaccine was
contaminated by an unrecognized avian retrovirus
with unknown safety implications.

4.2. Background
The usual flow of genetic information is from DNA to
RNA. However, the reverse of that process was
discovered to be mediated by an RNA-dependent DNA
polymerase (reverse transcriptase) that some RNA
viruses, such as retroviruses, use to reverse-transcribe
their RNA genomes into DNA. That viral DNA can then
be integrated into the host genome and replicated,
resulting in the production of more RNA virus. RT
activity has therefore been used as a biochemical
marker for the presence of retroviruses. However, the
genes that encode RT are widely distributed in
eukaryotic organisms and all reverse transcriptases
are evolutionarily related. In addition, cellular DNA-
directed DNA polymerases can exhibit some
ability to use RNA as a template and reverse-
transcribe as well.
AND Continues today: creating HOW Many New Diseases?
The Dangers of Xenotransplantation. Nature Medicine 1995
JP Stoye and JM Coffin

• Such viruses are widely distributed in mammalian species including

pigs and baboons, potential
donors for these procedures.
• Since they are inherited in the germ line in the form of proviral DNA,
• They are impossible to remove using the usual methods for deriving
pathogen-free animals.

• Implanting an organ carrying a dormant endogenous retrovirus into a

patient is equivalent to injecting the patient with live virus.
Xenotransplantation and Primates - Threats Masquerading as Cures.
September 1, 1996

• Dr. John Coffin*, a leading expert on recombination in viruses, concluded "the infection is a virtually inevitable
consequence" of xenotransplantation and "This is a very serious worry because the animals that have been
chosen for doing this -- the baboon and the pig -- are both known to carry endogenous viruses, replication
competent, but very poorly studied, that are capable of infecting human cells." He further suggested baboon
bone marrow experiments could make the HIV-AIDS infection "worse by spreading the host range."

• Despite scientific skepticism, the FDA supported the clinical experiment to transplant baboon cells into AIDS
patient Jeff Getty. Prior to this decision, the FDA convened lengthy hearings of the National Academy of Sciences'
Institute of Medicine and its own Biological Response Modifiers Advisory Committee. Dr. Marion Michaels*, from
the University of Pittsburgh, told the committee that despite rigorous screening, "the donor organ, the tissue or the
accompanying hematopoietic cells can also be the source of infection. Most often these infections are latent
organisms and are often clinically silent in the donor."

Isn’t Injecting babies and children with mouse viruses

capable of infecting human cells the same thing??
Current Vaccine schedules compound damage in vulnerable populations with Chronic
Disease and Cancer (20-30 Million Americans)
“Activation*of*the*cellular*immune*system*is*important*in*the*
pathogenesis*of*HIV*disease,*and*that*fact*has*given*rise*to*concerns*
that*the*activation*of*the*immune*system*through*vaccinations*might*
accelerate*the*progression*of*HIV*disease*.**.*.*If*feasible,*it*is*
preferable*to*have*patients*on*antiretroviral*therapy*(ART)*prior*to*
receipt*of*vaccination.”*– Accessed*May*3,*2013.
UCSF%Pediatric%Pediatric%AIDS%Website%on%HIV%and%Immunization

• Sterile environments result lack of educated immune systems

• Vaccination schedules result in anergic immune systems that is the inability to mount
an immune response to the antigen
• Toxic components exacerbate immune dysfunction resulting in aberrant expression
of host endogenous RVs
• Reappearance of disease is BECAUSE of inappropriate vaccinations and the toxic
components contained in them
 Conclusions
Aberrant evolution of the human genome by:
• Replication competent retroviruses generated laboratories in
current vaccines and cell cultures
• Increased zoonosis of novel retroviruses in human population
from animal populations.
• That means GMOs and toxins in animals result in compromised
immune systems and the expression of endogenous viruses ..eg
Bovine leukemia virus
• These retroviruses CAN and have been shown to infect human
cells and like HTLV, HIV are passed in milk and other fluids
• The blood supply is contaminated and the vaccines are
contaminated as is food supply (milk)
Phytocannabinoids can Enhance Vaccine Efficacy and Reduce Neuroinflammation