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Eleni Papadopulos-Eleopulos, Biophysicist Department of Medical Physics, Royal Perth Hospital, Western Australia, Valendar F Turner, John Papadimitriou, Barry Page, David Causer, Helman Alfonso
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We repeat: “Where is the proof for HIV
purification by any method?”
In his rapid
response entitled “If it’s Good Enough for RSV, Then it is Good Enough for
HIV” (24 June 2003), Tony Floyd wrote: “It has
been posited [sic posted] above [presumably he is referring to our rapid
response “Distinguishing between true and “official” HIV infection” 20
June 2003] that: >an individual positive in New York City on the
CDC criteria would not be positive in Sydney, Australia”. He comments
“How extraordinary”. We
agree. It’s the same virus and
the same test. Who would have
ever thought travel or emigration could cure HIV infection?
The HIV antibody test is the only test in the history of medicine whose
results have one meaning in one country or laboratory and another in another
country or laboratory. What
is even more extraordinary is that this fact does not seem to worry the HIV
experts.
Tony Floyd asks “Is
there even one patient that you are aware of that this theory would apply to?”
This is not
a theory. It is a conclusion
based on published data. In a
study entitled "False-Positive and Indeterminate Human Immunodeficiency
Virus Test Results in Pregnant Women" published in 2000, the authors from
the Departments of Paediatrics and Family Practice, University of Texas wrote:
"Under no circumstances should a patient be informed that she is
infected unless both the ELISA and WB test results are positive...Testing for
HIV is an emotional experience. An
HIV diagnosis may lead to depression, fear, anger and suicidal ideation.
Family, friends and community may ostracise infected people, and
relationships with spouses or partners may be jeopardised.
An indeterminate result can cause the same problems if the physician
misinterprets the result as being indicative of infection". (1)
They also pointed out that "It is possible for serum to be
positive by one set of criteria and indeterminate by another" (1).
The study “Transmission of Human T-Cell Lymphotropic Virus Type III (HTLV-III) by Artificial Insemination by Donor” (2) is considered to be one of the first to prove infectivity by semen and has been quoted ever since in support of this claim. The donor was considered as being positive on the basis of two bands (p41, p24) in the WB. Four of the women were considered to have been infected, two on the presence of only one band (one woman had p41 and the other woman had p24), the other two women on the basis of two bands (p41 and p24). At that time, the WB criteria was the presence of one band. In 1987 the criteria were changed but nobody re-tested either these women or (to our knowledge) any other person deemed to be infected on the basis of the pre-1987 criteria.
Tony Floyd
asks: “Is there anyone who, confirmed positive by all tests in New York,
would then not be positive by the usual series of tests in Sydney?” Answer:
What does Tony Floyd mean by “all tests”?
Both the US and Australia use the same testing algorithm.
The “usual series of tests” is a twice reactive ELISA followed by a
positive Western blot. There are
many publications (Tony Floyd can look them up) in which a particular study
states its criteria for a positive WB. These
include those of the CDC and interestingly that of the Multi-Center AIDS
Cohort studies prior to the early 1990s.
In the latter one “strong” band was defined a positive WB.
Assuming some of the 5000 gay men tested in this study fulfilled this
or the CDC criteria (the actual WB patterns are never published) then yes, an
unknown number of individuals, who tested positive in the US, would not be
positive in Australia. (Has Tony
Floyd ever wondered how our
National Reference Laboratory knows its criteria are proof of infection? He could email the Director and report back to this forum http://www.nrl.gov.au). Tony Floyd
asks: “Or is it just a one-in-a-million hypothetical?
In which case it deserves as much attention as the plethora of other
alternative AIDS arguments”. There is
nothing hypothetical about these data and there is no need for a “plethora
of” “alternative AIDS arguments”. Any
argument about a retroviral theory of AIDS begins with whether or not there is
such a retrovirus.
Tony Floyd
also wrote: “The
attempted side-step of Brian Foley's question deserves attention: What he
asked was: > If the Perth group believes that their method is valid for studying viruses, they should be able to name at least one virus which has been studied using their criteria. Where is the evidence that ANY virus has EVER been "purified" to their satisfaction? This was in
no way satisfied by merely providing references to a paper from 1961 about the
Rous Sarcoma Virus and from 1973 about the Murine Sarcoma Virus.”
Brian Foley
asked for evidence and anyone (including Tony Floyd) upon reading the two
references in our rapid response entitled “Where is the proof for HIV
purification by any method?” (19 June 2003) would be “satisfied”. If Tony
Floyd had read our rapid response (19 June 2003) carefully, he would have
realized that there was no need to give any “indication” “as to why the
papers might support the use of Density Gradient Centrifugation as a valid
means of proving the existence any virus these days?”
As we pointed out in our rapid response (19 June 2003), “Density
Gradient Centrifugation” has not been used only in 1961 and 1973 but has
been the “preferred technique for purification of RTV” for at least the
last 30 years. This was the
method used in the first studies (1983/1984)
(3), (4), (5) where HIV purification was claimed as well as in the last
ones (1997) (6), (7).
Tony Floyd
wrote: “Why have
even the two little known viruses mentioned not been associated with this
separation technique in the last 30 years?”
The simple
answer to this question is that there is no need for it any more.
The Rous Sarcoma Virus, as every virologist knows, is not a “little
known” virus but (perhaps with the exception of “HIV”) the best known
retrovirus for which Nobel prizes have been awarded.
Tony Floyd
wrote: “If you
did cite the 1961 paper on Rous Sarcoma Virus as an example of a virus
purified to your satisfaction, is it not ironic that RSV is a retrovirus very
similar to HIV? In fact the fusion protein and an envelope glycoprotein
precursor have been shown to be similar in both viruses(1)”
It appears
that this time Tony Floyd did not ever bother to read the abstract but only
the title of his reference 1 (8). If
he had read it, he would have realised that the abbreviation RSV in the title
of his reference has nothing to do with the abbreviation RSV for the Rous
Sarcoma Virus. The first
sentence of the abstract reads: “The
proteolytic cleavage sites of the human immunodeficiency virus type 1 (HIV-1)
envelope glycoprotein precursor gp160 and the fusion protein of respiratory
syncytial virus (RSV) show a sequence homology.”
Respiratory
syncytial virus (RSV) is not a retrovirus but a virus belonging to the family
paramyxoviridae, genus pneumovirus.
Tony Floyd
wrote: “If you
are satisfied about the purification of RSV, then why is HIV so different?” There has
been no publications of electron micrographs proving purification of HIV.
Tony Floyd
wrote: “Do you
except [sic accept] that there might be a chance that all the infectious
disease experts, virologists and vaccine developers around the world are
working with a very real virus called HIV?” All “the
infectious disease experts, virologists and vaccine developers” are telling
us that Montagnier proved the existence of a “real virus called HIV”.
However, Montagnier acknowledges that to prove the existence of a
retrovirus, it must be purified. Since
now Montagnier says that “I repeat, we did not purify” (9), why should we
or for that matter anyone else including Tony Floyd accept the existence of a
“very real virus called HIV”?
So the
question still remains: “Where is the proof for HIV purification by any
method?”
From the
title of his rapid response entitled “Faster
Progression to AIDS and Death Occurs in Those With Higher Levels of HIV VIRUS”
(4 June 2003), Tony Floyd obviously believes that high “viral load” means
high “levels of HIV virus”.
Could he please give us the evidence which proves that high “viral
load” means high “levels of HIV VIRUS”.
In his rapid
response entitled “Manipulations
and misrepresentation of scientific facts only serve to fuel HIV/AIDS” (30
May 2003), Tony Floyd extensively quotes William Makgoba’s statement made in
the South African newspaper, THE SUNDAY INDEPENDENT, and finishes by saying:
“Glad the truth is getting through where it matters most”.
Below is our answer published in THE SUNDAY INDEPENDENT, June 15 2003:
“How to resolve Aids dispute once and for all
In his
speech at the International Human Rights Network symposium in Switzerland (“Mixed
signals on Aids eroding confidence”, The
Sunday Independent, May 25), Professor Malegapuru Makgoba put the question
“A nutrition handbook, an African potato and some red herrings – are these
really South Africa’s responses to the HIV/Aids epidemic?”
A
better question necessitating an immediate answer is “Why are nevirapine and
AZT monotherapy good enough treatment for South African women but not American
women”? Makgoba
expressed the view “there has been a casting about for theories to
contradict the orthodox scientific findings on HIV/Aids, such as the
countenancing of discredited dissident theories”.
Scientific
theories are discredited in scientific journals with scientific data.
For
over fifteen years we have questioned the HIV theory of AIDS and published
alternative theories. Yet to date
no HIV experts have published any scientific data which discredit our views.
Furthermore,
they have done everything possible to prevent our publishing and continue to
claim, as Makgoba reportedly said, “There is little doubt that HIV causes
AIDS. In contrast, there is no
evidence that common African conditions such as poverty; malnutrition; and
many chronic infectious diseases by themselves, singly or in combination,
cause the characteristic immunodeficiency typical of Aids.”, that is, “the
progressive depletion of CD4+ cells”. It is a great pity Makgoba failed to consider the
eminent HIV/AIDS expert Piot and his group writing in Lancet in 1984. “Tuberculosis, protein calorie malnutrition, and
various parasitic diseases can all be associated with depression of cellular
immunity.” At the same time, similar views were expressed by
other HIV/AIDS experts such as Clumeck, Biggar and Quinn.
As far back as 1987 Canadian researchers stressed that before the AIDS
era it was known that "In TB as well as in lepromatous leprosy, an
immunosuppressive state will frequently develop in the host. This state is
characterised by T lymphopenia with a decreased number of T helper cells [T4
cells] and an inverted T-helper/T-suppressor cell ratio ...Immunosuppression
induced by the infection with M.tuberculosis can persist for life, even when the TB is not
progressive". The same researchers noted that TB was present “prior
to infection with HIV [prior to the development of a positive antibody test]
or development of overt AIDS” (Before 1987 TB was not an AIDS defining
disease). In other words, the presence of TB leads to a
decrease in T4 cells and the positive antibody test (“HIV infection”)
follows rather than precedes TB. In
1994 Essex and his colleagues
proved that mycobacterial infections
lead to the appearance of a positive antibody test which HIV experts consider
proof for HIV infection. They
concluded that “ELISA and WB results [the two antibody tests used to prove
HIV infection] should be interpreted with caution when screening individuals
infected with M. tuberculosis or
other mycobacterial species”, and that “ELISA and WB may not be sufficient
for HIV diagnosis in AIDS-endemic areas of Central Africa where the prevalence
of mycobacterial diseases is quite high”. According
to a 1998 Lancet editorial, the
developing world "bears more than 90% of the global burden of HIV
infection" and "Tuberculosis (TB) is the leading cause of death
worldwide among people with HIV". Professor
Abdool Karim has written that in South Africa “Clinically, pulmonary
tuberculosis (TB) is the main presenting illness among HIV infected persons”.
If
this is the case then the vast majority of cases of HIV/AIDS can be eliminated
simply by eradicating TB. This
can only be achieved by abolishing poverty and its consequences.
Could Makgoba please provide us with one single scientific study with evidence proving HIV is the cause of AIDS? With no effort spared to date we have been unable to find such a study. Also could Makgoba cite one scientific study with the evidence which proves HIV has been isolated/purified and thus it exists. According to Makgoba, “Scientific and political
controversy over HIV/Aids in particular is also not new.
In the late 1980s, for example, French and American scientists were
locked in ugly battles about who first isolated the HI virus... After detailed
investigation and scrutiny of the scientific literature and laboratory notes,
then presidents Ronald Reagan of the United States and Francois Mitterrand of
France signed an agreement that credited Dr Robert Gallo and Dr Luc Montagnier
as the co-discoverers of HIV”. Indeed, Montagnier’s group in 1983 and Gallo’s
group in 1984 claimed to have isolated HIV, that is, to have obtained the HIV
particles separate from everything else, namely, to have purified the HIV
virus. In a 1997 the French
investigative journalist Djamel Tahi interviewed Montagnier over his 1983 Science
paper where he claimed to have discovered HIV.
After repeated questioning Montagnier gave the stunning response that
in electron micrographs of what they called “purified virus”, even after a
“Roman effort” they could not find any particles with “the morphology
typical of retroviruses”. He added “I repeat we did not purify!”
When Montagnier was asked if Gallo isolated/purified HIV, he replied
“Gallo?…I don’t know if he really purified.
I don’t believe so”. The
lack of proof of HIV isolation/purification and thus of its existence by “the
co-discoverers of HIV” led us to propose an isolation experiment at the July
2000 Presidential AIDS Advisory Panel Meeting in Johannesburg.
This was to be carried out jointly by the Perth Group and HIV experts
from South Africa. It was agreed
by both sides including Makgoba that this experiment should be performed as
proof for the existence of HIV is the most basic tenet of the HIV theory of
AIDS. The
cost of this experiment is insignificant compared to the amount the South
African government spends on HIV/AIDS. Since
then, the HIV experts from South Africa and especially Makgoba have done
everything possible to prevent this experiment being carried out.
Why? Is this not the way to resolve the issue once and for all?”
(10)
References:
(1)
Doran TI, Parra E. (2000). False-positive and
indeterminate human immunodeficiency virus test results in pregnant women. Archives
of Family Medicine 9:924-9.
(2)
Stewart, GJ, Cunningham, AL,
Driscoll, GL, Tyler, JP P, Barr, JA, Gold, J Lamont, BJ (1985) Transmission of
human T-cell lymphotropic virus type III (HTLV-III) by artificial insemination
by donor. Lancet
ii:581-585.
(3)
Barre-Sinoussi F, Chermann JC, Rey F, Nugeyre MT,
Chamaret S, Gruest J, Dauguet C, Axler-Blin C, Vezinet-Brun F, Rouzioun C,
Rozenbaum W, Montagnier L (1983)
Isolation of a T-Lymphotrophic Retrovirus from a patient at Risk for Acquired
Immune Deficiency Syndrome (AIDS). Science
220:868-871.
(4)
Schupbach J, Popovic M, Gilden RV, Gonda, M. A., Sarngadharan, M. G., Gallo, R. C. (1984)
Serological analysis of a Subgroup of Human T-Lymphotrophic
Retroviruses (HTLV-III) Associated with AIDS. Science
224:503-505.
(5)
Sarngadharan M, G., Popovic M, Bruch L. (1984)
Antibodies Reactive to Human T-Lymphotrophic Retroviruses (HTLV-III) in
the Serum of Patients with AIDS. Science
224:506-508.
(6)
Bess JW Jr, Gorelick RJ, Bosche WJ, Henderson LE,
Arthur LO. (1997) Microvesicles
are a source of contaminating cellular proteins found in purified HIV-1
preparations. Virology Mar 31;230(1):134-44.
(7)
Gluschankof P, Mondor I, Gelderblom HR, Sattentau
QJ. (1997) Cell Membrane Vesicles
Are a Major Contaminant of Gradient-Enriched Human Immunodeficiency Virus
Type-1 Preparations. Virology
230: 125-133
(8)
Streckert HJ, Werchau H. (1992) Epitopes at the proteolytic cleavage sites of HIV-1-gp120 and
RSV-F protein share a sequence homology: comparative studies with
virus-induced and antipeptide antibodies.
Intervirology 34(1):30-7. PMID: 1385356
(9)
Tahi D. (1998)
Did Luc Montagnier discover HIV? Text of video interview with Professor
Luc Montagnier at the Pasteur Institute July 18th 1997. Continuum 5:30-34
(10)
Mhlongo S,
Turner VF, Papadimitriou JM, Alfonso H, Page BAP, Causer D, Fiala C,
Papadopulos-Eleopulos E. 2003, How
to resolve Aids dispute once and for all. The
Sunday Independent June 15, p7.
Competing interests: None declared |
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