Dr. Stefan Lanka answers critic Steven B. Harris M.D.'s rejoinder to his paper, HIV: Reality or Artefact

[Sheri Nakken]

more on my webpage
http://www.nccn.net/~wwithin/AIDS.htm
Dr. Lanka Chats With Dr. Harris
Dr. Stefan Lanka answers critic Steven B. Harris M.D.'s rejoinder to his
paper, "HIV: Reality or Artefact ".

http://www.sumeria.net/aids/chat.html

Dr. Steven B. Harris will no doubt consider it an impertinence even to
respond to his "rebuttal" of the thesis I put forward in my article on HIV
in the capacity of a "purported" virologist, striking as it does at the
very bedrock of his credo. I console myself that while I make no claims to
infallibility, I have no doubt that I am a virologist, moreover, one
motivated only by altruism, and untroubled by any worries that I may have
dispatched any friend or patient to an entirely unnecessary and painful
death, through craven obeisance to an ill-thought out medical theory
concocted by a French mediocrity who, right from the start, doubted the
validity of a virus-only theory of AIDS causation and only last week
unleashed a new wave of doubt; and an American scientific gangster who had
committed so many crass, self-aggrandising blunders in the previous decade,
that he could not really be relied upon to tell the time correctly.
I have also not forgotten the First Commandment of my profession: above
all, do no harm!
It is, of course, only supposition on my part to think that elementary cell
biology forms any part of the curriculum of medical training of American
doctors. If so, it is astonishing that Harris has either forgotten it all,
or is wilfully ignoring it, for reasons best known to himself.
That said, I must compliment my critic on his courage and relative
erudition, for it is not often that, in my admittedly still limited
experience of life, a mere doctor knowingly crosses swords with a molecular
biologist/virologist on the latter's home ground. Doctors are normally more
at ease speculating about the vagaries of epidemiology than engaging in
disputation with the practitioner of an exact science.
Harris's simple mistake is to have ignored well-known intracellular
structural particles common to all metabolically active cells, of which
there are many - specifically, what are called "coated vesicles". Their
function is to transport metabolic decay products out of living cells.
This is hardly a pardonable error, since basic prudence on his part should
have led him to study fairly closely the differences between electron
micrographs of microsomes in general, and coated vesicles in particular,
with or without the help of a specialist in this field - it did after all
form one of the two main planks of my article. Neither virus particles nor
cellular particles are rarities in the literature. Contrary to Harris's
little joke, I have spent an enormous amount of time in libraries, far too
much of it wasted trying to make sense of the mile upon mile of bookshelf
devoted to the riddle of "cancer-causing" viruses (of which more below).
Harris clearly would have benefitted hugely looking down an electron
microscope more often, and allowing himself to be enchanted by the
multiplicity of such "Harris" viruses, more widely known as coated
vesicles. This would have made him realise that their very ubiquity in
healthy tissues meant they could not be responsible for any pathogenicity.
Harris's strategy appears to be to launch a shut-out bid by declaring HIV
to be a lentivirus, as if that explained anything. Lentiviruses are an even
worse case of virological muddle than HIV, in that they, too, have never
been isolated nor proven to do what is alleged of them. Fiddling around
with them has been going on for 20 years at least - to no effect - whereas
with HIV it has only been 10! One very important difference, though,
between the two situations is that lentiviruses have at worst affected only
a handful of animals with so little consequence, that most scientists would
be hard pressed to say anything about them, whereas HIV has spawned one of
the worst mistakes in the annals of medicine, a veritable nightmare for
those affected, and a significant impairment of the quality of life of
those who just live in Dread of it.
Whether lentivirus or not, it is a nullity ab initio to seek to prove
anything in science by arguing by analogy. That is the negation of the
scientific method. Whatever may be true of FLeV, FIV, SIV etc. has no
bearing on the existence or function of HIV. Points of visual similarity do
not constitute proof of identity nor function. To assert otherwise means
either that he has never looked properly at electron micrographs, or he is
deluding himself.
The fatuity of his reasoning is highlighted (quite fortuitously) by the
recent "discovery" that HIV is most definitely not a lentivirus. Lenti-
means slow. Because since January 1995, don't we have it on the highest
authority that HIV replicates very rapidly, at a rate of 1000 million
particles a day, every day, for an average of 10 years? Anybody with an
ounce of common sense must have realised that a virus cannot have been
barely detectable for the first 10 years of its existence, then suddenly
turn out to be "hyperactive" after all. The answer to this conundrum is
quite simple: AIDS science is not science at all, just empty posturing as
such. Proper science is never made at press conferences, it does not
operate by decree, it is not a matter of developing a consensus, and it
should not totter from "revelation" to "revelation", with theory made "on
the hoof", a hodge-podge of mysterious mechanisms requiring further
billions to finance an army of scientific bureaucrats.
Inexplicable failures in the predictions of a scientific theory should
spell its death. That is the essence of the scientific method. Consistent
failure in respect of HIV should long ago have sufficed to dismiss it as a
cause of AIDS. That it continues nonetheless, makes it just an article of
faith, and reduces belief in it to the status of a religion.
An analysis of Dr. Steven B. Harris's answer to my paper "HIV: Reality or
Artefact " has just appeared in Continuum Magazine
(London), June/July 1995 (tel +181 961 1170, fax +181 961 2330).
The format adopted there was of stating the point at issue followed by
Harris's comment with my answer to that, juxtaposed. To pursue this format
here would clearly become very unwieldy, and the use of photographs on
e-mail transcends my technical expertise. I have, therefore, summarised the
points raised by Harris, and appended my answers to them.
Dr. Harris is clearly quite an intelligent man, so his very first point
"Strangely enough, Lanka does not explain what we're seeing in all those
electron micrographs" has me tearing my hair out, because a few paragraphs
further down he provides his own answer that "less well-known is the
existence of other particles which look like viruses but aren't, and are
nonchalantly referred to as "virus-like" particles. Such particles are far
from rare, found, for example, always in placentas, and very frequently in
the artificial environment of laboratory cell cultures. They have served to
muddy the waters considerably as far as AIDS research is concerned, because
particles just like these have been called HIV."
What is one to make of such crassness? Is the whole AIDS tragedy currently
being played out just a little game for Harris? It is a property of all
biologically active cells that they contain intra-cellular particles called
microsomes, perixomes and lysosomes, which are particulate in nature, and
to the untutored eye could be mistaken for virus particles. Harris seems to
forget that most people can actually think, and flip back to see what has
been said before, a number of other such howlers (deliberate deceptions?)
will be pointed out below.
Harris then describes some properties of lentiviruses, which are an
entirely separate issue. It is true that while these have a recognisable
shape (as opposed to being just an amorphous mess), and do indeed have what
appear to be knobs (the famous CD4 receptors) which shear off so easily,
this to a proper scientist does not suffice to make them viruses. Sorry!
Microsomes, perixomes and lysosomes also have recognisable shapes and many
have spikes of some kind on them. The important point Harris cannot or will
not comprehend is that these lentiviral micrographs are never of the
viruses he is so fond of quoting, but are always interspersed with other
structures and debris, which is crucial to my case.
Harris goes on:
"HIV-1 and HIV-2, the two viruses isolated from human AIDS patients..."
If they had indeed been isolated, as he claims, nothing further need be
said; the whole point is that they have not been isolated, indeed, the
title "isolated viruses" occurs several times in my references which does
not mean they have actually been isolated, of course.
Harris's attitude is quite extraordinary. He admits that "there are
existent studies in which less than perfect-looking particles have been
called HIV, and assumed to be HIV, but some of these studies have no doubt
also seen cellular debris or other retrovirus which can be mistaken for HIV
or other lentiviruses if not all identifying features are present. However,
there are quite enough studies in which all the lentivirus characteristics
noted above ARE present in EM photographs, and morphology is considerably
more clear. In these studies, the viruses in the electron micrographs are
clearly either EIAV, FIV, SIV, or HIV-1, or HIV-2."
Yet the caption to the micrograph Harris quotes repeatedly, clearly states
"sections of co-sedimented HIV and latex spheres ... along with membranous
and macromolecular debris ..." Out of his own mouth therefore he admits
that these isolated particles are not true isolated particles, but a
heterogeneous mixture containing unspecified impurities. What is the matter
with the man! In case anybody is wondering why there are latex spheres
present in Harris's virus isolation: well, they are there to stop the
particles from crushing each other. In other words, if they were not there
all the "HIV" particles would disintegrate. The use of latex condoms may
therefore be contra-indicated, because they may inadvertently - by an
indirect mechanism, naturally - keep HIV particles viable by stopping them
from crushing each other in the ejaculate. Just a thought, anything is
possible in AIDS science.
Harris then turns his sights on the section in my original paper in which I
explained how it came about that retroviruses were long suspected of
causing cancer. He says:
"This is, in general, untrue. Not all cancers were blamed on viruses. Many
viruses, such as FLeV, FIV, SIV, and even DNA viruses with reverse
transcriptase activity, like hepadnaviruses in woodchucks were proven
experimentally to cause cancer in lab animals, and even in random source
animals (pet store animals, such as cats) brought to the lab and given
virus."
Is this an answer? Does this explain which cancers were thought of as being
due to viruses and which not? I consider it decidedly sick of Harris to
juxtapose cancers in woodchucks, pet store animals and cats with the
ongoing curse of our age, real cancers of many kinds. Is he really so naive
as to believe that the billions of dollars devoured annually by the NCI in
the US alone was to deal with cancers in woodchucks and cats?
What is the point of making excuses now about the mass failure by the
scientific community then, and to wax eloquent about some detail about HIV
which he finds "elegant". The fact of the matter is that then, about
cancer, as now about HIV, the fundamental science is wrong, and no amount
of epidemiological soft soap "isn't it funny that ..." can rectify it.
Moreover, he was not himself responsible for this fiasco, so why is he
bothering to defend it. He has enough on his conscience with the present
situation.
The War on Cancer declared by President Nixon on 23/12/1991, based on the
notion that viruses cause cancer implied that all cancers are caused by
viruses, for one thing because those researchers who did not accept this
were ignored and de-funded. It is a gross deception, like everything to do
with HIV and AIDS is in our time, to say otherwise. To grasp what was
produced in a test-tube and what is still being produced in them, I
strongly recommend reading the paper by Peyton Rous (J Exp Med, 1911, 13,
397), especially noting his comment:
"The first tendency will be to regard the self-perpetuating agent active in
this sarcoma of the fowl as a minute parasitic organism. Analogy with
several infectious diseases of man and the lower animals, caused by
ultramicroscopic organisms, gives support to this view of the findings, and
at present work is being directed to its experimental verification. But an
agency of another sort is not out of the question. It is conceivable that a
chemical stimulant, elaborated by the neoplastic cells, might cause the
tumour in another host and bring about in consequence a further production
of the same stimulant".
The ludicrous situation in which contemporary cancer research has
maneuvered itself into is described by Gerald B Dermer, who provides the
evidence that cancer in vitro and cancer in vivo have nothing to do with
each other.
So let us look in some detail at what Harris thinks is an isolation of HIV
(Virology, 1992, 189, 695). It bears the inauspicious title "Factors
underlying spontaneous inactivation and susceptibility to neutralisation of
Human Immunodeficiency Virus", which rather suggests that it is not a very
stable entity, as indeed it isn't. So unstable, in fact, that it
disintegrates spontaneously.
What one then sees on page 700 is nothing other than a preparation of the
above mentioned cellular particles, which are of different sizes and
shapes, and, as the caption clearly states, are contaminated with
"membranous residues" and "macromolecular fragments". This is not what an
isolated virus preparation should look like. What they should look like can
be seen in any virology textbook (and shown in Continuum). When real
viruses are isolated, they do not need "fixing", which means embedding them
in a resin to stop them from falling apart, nor slicing into ultra-thin
sections to show up detail, only then being in a fit state to be
photographed in an electron microscope. Isolated virus preparations should
contain no impurities, and after staining in one piece to give contrast,
are ready to be photographed. All particles should look alike. All viruses
that are real, have been isolated and photographed in this way. The reader,
open-minded AIDS researchers and especially Steven B. Harris could do worse
than look at the publication about a virus in whose isolating and
characterisation I myself was involved in (Virology, 1995, 206, 1, and
Continuum).
Harris gets himself into deep water by trying to come to grips with "hard"
science by questioning my contention that the correct characterisation of
viral proteins has not been performed.
What is needed are photographs of the native gels of the proteins and of
the nucleic acid, so as to prevent the skulduggery, as we shall see.
Harris thinks the missing proteins of HIV are found in the Cohen et al
paper. But all that we see there is more fiddling and tinkering with the
evidence, which in a criminal case would land him in prison for suppression
of material evidence. We see the result of radiolabelled SDS (detergent)
polyacrylic amid gel electrophoresis (PAGE). One needs to see the proteins
on the SDS gel before antibodies to it were formed and radiolabelled. If
you have something to show, and above all if you want to prove that the
proteins of a virus have been isolated and separated according to size,
then the native gel has to be shown before further experiments are
conducted. This is standard procedure - except, of course, in this case
where it really matters! If you attempted this with HIV isolations you
would find that many proteins wouldn't fit in with the conventional HIV
model. To get round this problem, only photos of certain antibodies which
bind to selected proteins are shown, and the other proteins, which remain
unbound by antibodies is not revealed. Only selected proteins are made
visible by binding to antibodies, because only pre-selected proteins are
used to inoculate experimental animals which are used to produce, with
which these proteins are detected. The same applies to humans in whom only
antibodies to proteins are produced with which they had previously been in
immunological contact, i.e. inoculated with (except rheumatism and
autoimmune disease). It is quite a difficult argument to follow which will
leave many a head spinning, but that is how AIDS science works.
Variations of an original error (Ratner et al.) may enchant Harris, but
remain an error just the same. They show once again that something has been
obtained from the cell soup, not from a virus.
Harris goes on to explain that the evidence that the knobs attach HIV to
cells is "massive", as if he had the requisite training to evaluate the
evidence.
The evidence of 100,000 papers on HIV and AIDS should indeed be massive;
unfortunately (or rather, mercifully) not one of them contains any direct
evidence for the existence of HIV nor of its components. What is required
is a standard isolation experiment, not something fanciful like sprinkling
cloned DNA on to cell cultures and seeing what happens.
That they throw some mouse genes into cell cultures and produce something
mouse-specific, is just modern alchemy. That resistance to antibiotics is
also been bred in, transgresses against all scientific decencies, paid for
by us, the taxpayer. Such misuse of public money is quite appalling. How
can it be justified? It is scientifically unacceptable to dream up
explanations of what went wrong, and proceed as if nothing of significance
had happened, as is usually the case in AIDS "science".
We now join Alice in Wonderland in which Harris explains in greater detail
how this "science" works, to wit, the concept of "co-purification",
hitherto unknown to science.
He says "these are the same proteins which are coded for by the viral
genome, and which co-purify with the infectious virus on sucrose gradients,
as noted above. Why does it take a stretch of the imagination to image that
they are viral proteins?"
Answer:
Something that co-purifies with something else is of no interest to anyone.
Individual proteins should have a density that is entirely different to
complete viruses, and should for that reason not band at the same density
as viruses! It seems that these researchers have never even learned the
ground rules of cell biology and virology. The quality of evidence that
convinces Harris is frightening.
To try once more: second and third generation tests use synthetic proteins,
clearly therefore they are not viral. How can something that is synthesised
be viral. A virus is a creation of nature. Their use is an attempt to
maximise reproducibility. Is that really so difficult to understand?
We now come to various observations where Harris finds it expedient to act
dumb. In my original paper I quoted from the instruction leaflet
accompanying one test kit, namely,
"The test for the existence of antibodies against AIDS-associated virus is
not diagnostic for AIDS and AIDS-like diseases. Negative test results do
not exclude the possibility of contact or infection with the
AIDS-associated virus. Positive test results do not prove that someone has
an AIDS or pre-AIDS disease status nor that he will acquire it" Harris
feigns incomprehension. The significance of it is that the manufacturers
are aware of the difficulty of interpreting any result, because from
experience they know any number of conditions unrelated to HIV/AIDS can
test positive, equally that people can test negative and "indeterminate",
yet still develop AIDS. Harris then goes in for some face-saving goal post
moving by introducing the novel orthodoxy that not all HIV-infected people
develop AIDS.
I originally observed that some HIV researchers have tried to circumvent
the problem by pointing to something called "direct" evidence for the
virus. All that this meant, though, was arbitrarily selecting a protein of
a certain size which happened to coincide with that shown in HIV models.
The delusion of such "evidence" was illustrated when the protein later
turned out to be of human origin!
to which Harris answered: "neither gp-160 nor the viral reverse
transcriptase of HIV (which is magnesium dependent, unlike any in your
cells) are of 'human origin'. You will find none in any human cell
uninfected with HIV. Both are coded in the genome of HIV".
p24 is the direct evidence for HIV as far as most HIV researchers are
concerned. Steven B. Harris tries to distract attention by using reverse
transcriptase and gp160, which have never been considered in this context.
gp160 is nothing other than a cellular precursor protein, and the famous
reverse transcriptase is not even correctly demonstrated, because the RNA
template used for this is readily converted into DNA by cellular DNA
polymerases. The magnesium ion argument, therefore, is just another damp
squib.
If reverse transcriptase were really proven, which is questionable given
the lamentable state of AIDS research, then it would have to be encoded the
special cell lines need to make HIV. Where's the problem?
We now come to one of the 3 essential points of my paper, namely, to
explain what actually happens when they try to prepared HIV. Harris
dismisses it as "a sorry tale" and "baloney". This is hardly an answer,
though I appreciate that it is all he can do. It is pretty obvious that
Harris's grasp of all of this is pretty tenuous, and a successful rebuttal,
if there were one, is well and truly beyond his grasp of the subject. Since
I consider the AIDS disaster is anything other than a joke, I can only
advise him to put a cold towel over his head, check out my references, and
come up with a better answer.
Needless to say Harris's standing does not rise in anybody's eyes when he
has to rope in Gallo's problem to help him out. How fatuous to rebut one
non-existent virus with another non-existent virus. Does he really think
Gallo didn't prepare HTLV-III but did HTLV-I? It is surely obvious to
everyone by now, that Gallo has never done anything right in his life. Has
Harris not read the Crewdson Report in the Chicago Tribune; is he unaware
of the Office of Scientific Integrity's findings; is he not aware that
Gallo has finally got the push from the NCI? Yet he has the nerve to bother
people with some problem Gallo may have had cooking the books.
What an insult of an answer for Harris to waffle on about cross-reacting
sera. If one does not know the answer to a problem, the correct answer is
to say "I don't know". No-one can adjudge a technical problem on a highly
specialised subject not in his field. Flu vaccines, hepatitis B and malaria
all cross-react with HIV tests; whether a horse virus nobody has heard of
nor cares about, also does so is about as relevant as the price of tea in
China.
It is perfectly understandable that Harris has difficulty in rebutting the
template switching and hybridisation arguments put forward in my paper. I
am a virologist, and this is pure virology. Does he think I woke up one
morning and said to myself "let's play silly buggers, and put it about that
HIV didn't really exist." Of course not. No doctor could possibly rebut it
without the help of a top-rate virologist. If a Duesberg tried, I'd pay
attention, but talk of sera and antigens, what next! Harris then gets
carried away rather by his own rhetoric in saying "actually, one cannot
help asking why nobody has spotted the flaw in Lanka's argument, which
suggests that "HIV DNA" must be in every normal cell, since HIV as a
separate entity does not exist, and therefore no DNA PCR test can ever be
"negative" on anyone. Yet these tests routinely find no HIV DNA in HIV
negative people."
One major difference between what I have suggested and what the
AIDS-Establishment blithely accepts, is that the former is a working
hypothesis offered in the spirit of true scientific endeavour, subject to
revision and intelligent criticism, whereas the latter is totally failed
dogma.
It is my humble opinion that the sequences are endogenous, and anybody can
prove it. Not only in man, of course, but also in the special cell cultures
that always have to be used to make HIV. But here's the rub, dear Dr.
Harris! That is how HT23 (the first human retrovirus) was discovered in
1975, but which Gallo very soon thereafter had to withdraw from the
"market", because vociferous ape virologists staked an earlier claim to it.
This also explains why Gallo and Montagnier published almost identical
sequences, because he had purloined them as endogenous sequences from
Montagnier; only illicit collusion could have produced the concordance that
was obtained. Not only between these two, but also between Robin Weiss,
although the Pasteur Institute has up till now not sued him for patent
infringement. The evidence is available at the Patent Office in London for
all to see.
One reason why in the so-called PCR controls nothing is found, is that the
human cells used to act as controls, are not stimulated (stressed) in the
same way as those in which one wants to detect HIV, ie. they don't compare
like with like. The RNA detected in PCR tests is not expressed under normal
conditions, because they do not belong to the normal repertoire of nucleic
acid. The RNA detected is formed in response to stress when cells in short
term cultures begin dying, or are treated in such a way that its cellular
activity is disturbed, and "retroviral sequences" are expressed which are
not formed (transcribed) otherwise.
PCR only detects very short stretches of DNA that in this case are supposed
to be components of the genetic material of viruses. If one succeeds in
this, it is immediately described as "PCR positive", implying that the
remainder of the genetic material ascribed to HIV, is found somewhere else.
This is pure guesswork!
On careful reading of Harris's references on PCR and many others, one
discovers that a number of PCR tests for viral RNA use chromosomal DNA as
controls! As every genetics student would object immediately, this can't be
done. Transcription into RNA changes the gene sequence, ie. the RNA is
"edited"; on reverse transcription back into DNA it is no longer the
original DNA.
Starter molecules needed for this edited DNA are now prepared which fit
this DNA, but not the original. Herein lies the wizardry! A wonderful piece
of deception, and available for all to see! All recounted history!
Regrettably, with terrible consequences. The argument is tricky, and if
Harris can't or is reluctant to grasp it, then so be it. I have never
claimed that HIV DNA is present in every human being, for the obvious
reason that it doesn't exist except as a lab construct.
Harris asks:
"then why does a positive test give you a 50% chance of dying of
immunodeficiency in 10 years? That's a harsh punishment from rheumatology
and sunbathing. And why do positive antibody tests correlate so well (both
positively and negatively) with viral culture tests (which measure a
protein) or with direct PCR (which measures DNA)."
Answer:
I presume Harris means "have a 50% chance of dying of AIDS not
immunodeficiency". Or does he not know that they are not synonymous, given
some of his silly pat answers, I think he's not sure? Only 39% of AIDS
cases have anything to do with immunodeficiency. It appears to be all the
same to Harris. HIV kills off T4 cells, therefore 10% of people get
Kaposi's Sarcoma, 6% develop dementia, 3% develop lymphomas and 19% waste
away.
Or is this the point at which the "fiendishly clever" effect of HIV comes
in, whereby it causes these totally disparate diseases "indirectly", by
molecular mimicry, by apoptosis, by autoimmunity, by protein toxicity? If
Harris knew anything he'd know that he knew nothing: immunology is
essentially still in the Dark Ages, scarcely more advanced than mechanics
was without Newton.
By the way, is it another slip-up by Harris saying "have a 50% chance of
dying"? Is this now official policy - only half the HIV positives develop
AIDS? Since when, and why, or is it really 90% as he states further down?
Or don't all people with AIDS ultimately die?
Harris asks:
"if there's no virus to explain all this, how does Lanka explain it?
Remember, one must explain not only why people who test positive for "HIV"
antibodies almost always test positive for HIV by culture and PCR (which
don't test for antibodies), but also why people who test negative for
antibodies test negative by culture and PCR (see last set of 4 papers
quoted)".
Answer:
Thank you, Dr. Harris, but I do not need lessons on what constitutes a
proof in science. That you suddenly let on that you know, too, makes me
wonder why you have been so complacent in all your "proofs" up to now.
I suppose I do have to spell it out, superfluous as it seems. It is not
disputed that "HIV positives" are in some way at risk. The question is how
and of what.
I strongly urge readers to study carefully the papers cited by him to
understand why, in HIV negatives, PCR is also apparently negative. It is
quite simply because they never compare like with like, and play a dirty
trick on top of it all. The first HIV PCR studies gave no concordance at
all between antibody and PCR tests. Nowadays, this is glossed over, and in
those cases where this can't be done, it is claimed that HIV is present
only in the mutated, defective or non-integrated form. In summer 1993 (see
my original paper) they invented the concept of "molecular mimicry" to
explain the inexplicable: it says that the virus has mutated so much that
in effect it has mutated itself out of existence.
Harris's claim that "HIV is the only variable which independently
correlates with AIDS risk in all AIDS groups. None other has been found."
Answer:
The first howler is for him to assume that AIDS is the same disease in all
groups. It isn't! How many IV-drug addicts have Kaposi's sarcoma? Which gay
man has invasive cervical cancer? Is Harris not aware of the 1994 CDC
announcement that there cannot have been any HIV in Factor 8 given to
hemophiliacs, since drying of blood products reduces the risk of infection
to "essentially zero". But enough of such crass question begging answers.
I am aware of Harris's dismissal of the alternative drug intoxication
theory. I assume he is relying on the Winkelstein et al. paper, and no
doubt assumes that is the end of the matter. I can only rejoin that if he
is so naive as to rely in any way on the accuracy of self-reported drug use
- just as an aside, who the hell knows what people really take in when
shooting up, swallowing or sniffing adulterated illegal drugs prepared in
back street labs? Has he never been in an organic chemistry lab and noted
the nasty reagents that are used and the residues and side reactions, if so
he would be less cocksure.
The other - oh, so hard to quantify, so let's forget all about it - factor
is the effect of a psychological death sentence of a positive diagnosis. As
a virologist I cannot either, but as a human being I know it to be extant,
and I cannot just forget about it as Harris seems to with such insouciance.
Harris:
"There is no evidence that these drugs (AZT and its analogues) produce
deficits in the cell-mediated immune system which are important clinically.
There is no evidence that they produce AIDS (as Lanka may be trying to
suggest here) and a great deal of evidence they don't (the Concorde trials)."
Answer:
If Harris had any understanding of chemistry and were altogether less
intellectually dishonest, he would know that AZT was designed to kill cells
indiscriminately. He would take the trouble to find out how it does so. He
might also have read the book by Nussbaum "Good Intentions" which
chronicles in great detail the shenanigans, whereby AZT was resurrected as
an "anti-viral" when previously it was cytotoxic. He would also then
realise that misguided gay rights agitators were responsible for this
horrendous state of affairs, for which they and a whole lot of completely
innocent people are now paying the price. He would then realise that AZT
cannot by waving a magic wand (serendipitously?) help AIDS patients after
all, say, the way a natural product like aspirin, jojoba and primrose oils,
just might. If he, further, had any grasp of pharmacology, he would know
that different people manifest different degrees of drug absorption and
drug metabolism. And just a little thought on his part would tell him that
if you reduce the dose of even a toxic drug to a low level, no harmful
effects might be manifested. He might also realise that people don't always
tell the truth, and flush nasty things down the toilet.
Dr. Harris is pretending that the immune system is properly understood. I
hazard a guess that at most 1% of what it really comprises is known, hardly
a proper basis for dogmatism. Least understood is the significance, if any,
of T-cell counting. Harris would get the most up-to-date critical review of
current knowledge on this troubled subject by reading Eleni
Papadopulos-Eleopulos et al. in Genetica, April 1995. And when he has done
that he would benefit by swatting up on the whole murky topic of antibody
testing and PCR in Bio/Technology, June 1993, by the same authors. He will
become a wiser man.
I know someone who has for several years had only three T4 cells, which he
named after his dead friends. He himself is well. Dr. Felix Konotey-Ahulu
of the famous Cromwell Hospital, London, has described a tribe in Ghana
whose average T-cell count is only 100!. Also, why can an individual have
twice as many T-cells in the morning as in the evening? Is this also "just
baloney". Certainly not, it is all well documented. These arguments are all
just conjecture, and only tangential to the question whether HIV exists or
not and how it was "manufactured"; dealing with them thoroughly would open
up a whole new can of worms, beyond the scope of this response.
Harris denies that up until recently, being HIV positive did not constitute
a definitive prognosis of death. Since when is it "official" that 10% of
positives will be alive after 15 years? I thought you said it was 50%
(earlier on, remember?), or is that to be understood as meaning 40% die in
years 10 to 15? In German, there is a saying "Luegen haben kurze Beine"
(lies have short legs, ie. they don't get you very far). Stop making policy
on the hoof, it won't work. Long-term survivors have only been officially
recognised for the past 2 years, now you claim they are recognised to
constitute 10-50%.
Harris wobbles uncertainly around what AIDS diseases are. Destruction of
the immune system, eh? Dementia, cachexia, lymphomas and Kaposi's sarcoma.
Remember, "Luegen haben kurze Beine."
Despite the flawed nature of Dr. Harris's response, I would nonetheless
congratulate him on a creditable effort. It surpasses by far anything that
I have ever come across before, and contrasts sharply with the lamentable
position of most AIDS scientists who are satisfied with the statement: "the
evidence that HIV causes AIDS is overwhelming, though we still don't know
precisely how."
The correct position is that the evidence which is there is none, and
absolutely nothing is known about how it is supposed to do so.
ADDENDUM.
In his impressive SKEPTIC article, in which he satisfies himself that there
are no causes of AIDS other than HIV, he nonetheless blows the whole gaffe
by reaching the following two conclusions:
That AIDS will not spread beyond its present (tiny) risk groups.
That AZT has no useful function.
He seems not to have realised that he has thereby taken the ground from
under the whole AIDS construct, for, were it not "official" that AIDS can
afflict anyone, the enormous public funding for AIDS research ($96 annually
per heart patient vs. $36,000 per AIDS patient) would not exist; and
equally, if the vast profits accruing to Wellcome through AZT fell by the
wayside, the whole edifice of direct and indirect funding of HIV research
would grind to a halt. As Kary Mullis observed a while ago "who wouldn't be
infinitely fascinated by how HIV causes AIDS if there is a $2,000 million
price tag attached to the question every year". As an assiduous student of
epidemiology Harris might ask himself, why has HIV not spread, as according
Farr's Law it should have done?

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Sheri Nakken, R.N., MA, Classical Homeopath
http://www.nccn.net/~wwithin/vaccine.htm
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Sheri Nakken, R.N., MA, Hahnemannian Homeopath
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