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Cashing in on our Sex and Retroviruses

There are serious problems with the idea of testing for a retrovirus called HIV.

First of all, no one has given any explanation of just how that retrovirus is thought to degrade people's immune system. As a matter of fact, it cannot be isolated in sufficient quantities in the blood or tissues of people suffering immune deficiency to be doing what a virus is supposed to be doing.

But here is a central point that Cal Crilly brings out in this article: If that retrovirus, or rather the protein fractions we associate with antibodies to that virus, are present indistinctly in healthy and sick people, why are we testing at all?

Cashing in on our Sex and Retroviruses

by Cal Crilly

What is a HIV antibody test?

Does anyone know what the HIV antigens mean?

Here are the HIV numbers, do you think they are specific?

They were picked out of a hat in 1984.


"The major antibody specificities detected in HIV-1 WB analysis include gp160, gp120, p65, p55, gp41, p40, p31, and p24. To be reported as positive, the WB assay requires reactivity against the gp41 and gp120/160 bands encoded by the env (gp160, envelope glycoprotein) gene or against either one of these env bands plus the p24 band encoded by gag [Pr55(Gag)]."
Interpretation of HIV Serologic Testing Results

So p24 antigens or 'HIV core proteins' are found in cell transport, yes a piece of 'retrovirus' appears when moving or trafficking things around the body.

The HIV antibody test sees these and the result claims you have AIDS, it is literally a lottery.

- - -

"The trafficking of proteins in the secretory pathway is mediated by vesicles. Proteins of the p24 family are present on the membranes of secretory pathway organelles (ER, Golgi, COPI and COPII vesicles). Evidence exists showing that p24 proteins play a role in the development of Alzheimer's disease, making them an interesting research subject. Their presence in the secretory pathway and their tissue-dependent expression levels suggest that p24 proteins are involved in secretion. However, their molecular function is not clear. Several potential functions have been proposed for p24 proteins: (1) that they function as receptors for selected cargo; (2) that they regulate vesicle biogenesis; (3) that they perform structural and morphogenetic functions in the secretory pathway; (4) that they are responsible for quality control of transported proteins. In this article, we provide a critical review of the postulated functions of p24 proteins." 2010
The p24 family proteins--regulators of vesicular trafficking

We also find cell transport with gp120 from 'HIV' in a glucose transport protein called GLUT4.

"Our previous studies demonstrated that the expression of gp160 is also limited to fat and muscle tissues, where it is localized exclusively in GLUT4-containing vesicles, and thus, it represents a marker protein for insulin-activated glucose transport." 1994
The major protein of GLUT4-containing vesicles, gp160, has aminopeptidase activity

We find gp120 and p24 in the placentas of women who were not HIV positive.

"Antigens gp120 and p17 were identified in normal chorionic villi in vimentin-positive fibroblast-like cells and in endothelium, respectively. Antigen p24 was localized to HLA-DR positive cells that morphologically resembled macrophages in areas of villitis." 1991
HIV proteins in normal human placentae.

And gp160 in normal placentas.

"Expression of intact endogenous retroviruses by normal placental villous trophoblast and immuno-crossreactivity of villous trophoblast with anti-retroviral antisera have been documented. The nature and/or potential function of these particles/proteins has not yet been fully defined. We previously reported that monoclonal antibodies directed against HIV-1 envelope and gag proteins react with normal human villous trophoblast. In this study, we report that extravillous trophoblast (EVT) from second- and third-trimester tissue are also cross-reactive with anti-HIV-1 gp120/160 and p17/18 antibodies." 1995
Expression of endogenous HIV-1 crossreactive antigens within normal human extravillous trophoblast cells.

And gp120 and gp41 in tumours of reproductive tissue.

"RAK antigens p120, p42, and p25 exhibit molecular and immunological similarity to the proteins encoded by human immunodeficiency virus type 1 (HIV-1) and are expressed by 95% of breast and gynecological cancer cases in women and prostate cancer cases in men.

"Breast cancer DNAs of 40 patients were PCR amplified with HIV-1 gp41-derived primers, and all of the samples were found to be positive. The DNA fragments amplified in seven blindly selected breast cancer samples were sequenced. The breast cancer DNA sequences showed at least 90% homology to the HIV-1 gene for gp41. Antisense oligonucleotides complementary to the HIV-1-like sequences inhibited reverse transcriptase activity and inhibited the growth of breast cancer cells in vitro. Viral particles detected in breast cancer cell lines were strongly immunogold labeled with the anti-HIV-1 gp120 MAb. The results obtained strongly suggest that the long-postulated breast cancer virus may, in fact, be related to HIV-1." 1998
Human Immunodeficiency Virus Type 1-Like DNA Sequences and Immunoreactive Viral Particles with Unique Association with Breast Cancer

In ovarian cancers with gp41.

"PCR with HIV-1 Env-derived primers revealed DNA sequences with over 90% homology to HIV-1 gp41 in syncytia and in ovarian cancer cells but not in normal ovary cells." 1999
Giant Syncytia and Virus-Like Particles in Ovarian Carcinoma Cells Isolated from Ascites Fluid

And cervical cancers with both p24 and gp41.

"While investigating whether proteins retrieved by cervicovaginal lavages (CVL) from women with cervical intraepithelial neoplasia (CIN) might correlate with risk of progression to invasive cervical cancer, we unexpectedly identified HIV gag and env glycoprotein in CVL from women with HIV-negative serology. HIV antigens were consistently identified by mass spectrometry (MS) in CVL from 4 women but were absent in CVL from the remaining 16 women. HIV serologies of all 20 patients were negative for both HIV-1 and HIV-2 antibodies."

"WB and IC results demonstrated the presence of HIV-1 gp41 and p24 antigens in four CVL that were identified by mass spectrometry to have the HIV proteins. Despite negative serology, HIV RNA in CVL and HIV p24 in cervix biopsies were detected in patients with HIV antigen-positive CVL. HIV p24-positive CVL were PSA negative. All 20 subjects remained HIV seronegative throughout the study. Women with HIV proteins and RNA were comparatively older." 2009
Human immunodeficiency virus (HIV) antigens and RNA in HIV-seronegative women with cervical intraepithelial neoplasia

With gp41 in prostrate cancer too.

"Breast and gynecological cancer-associated antigens RAK p120, p42 and p25 exhibit molecular, immunological and genetic homology to HIV-1 proteins. Normal tissues, including the majority of tissues adjacent to cancer, do not express these unique cancer markers. Antigens RAK are now detected in 100% of prostate cancer and in the majority of prostate benign hyperplasia (BPH) cases. Polymerase chain reaction (PCR) with HIV-1 gp41-derived primers revealed prostate cancer-associated DNA fragments of similar size (140 bp) as in HIV-1 genome. Ninety-five percent of BPH samples obtained from prostate cancer patients tested PCR-positive. For comparison, only 61.9% of BPH samples obtained from cancer-free patients tested PCR-positive. The DNA fragments amplified in prostate cancer and in BPH showed more than 90% homology to the HIV-1 gene for gp41. The obtained results strongly suggest that a retrovirus related to HIV-1 may be associated with cancers of the reproductive system." 1998
Prostate, breast and gynecological cancer markers RAK with homology to HIV-1

So the HIV antibody test chosen in 1984 to define AIDS was just one highly paid scientist picking some antigens out of a hat that appear on cancer and fetal trophoblastic cells or perhaps simply in reproducing cells.

Then it was applied commercially to test blood banks believing 'retroviruses' were 'infecting' the blood supply.

Hemophiliacs were already getting immune problems from Factor VIII and the corticosteroids they received for Factor VIII allergies.

Only one third of Robert Gallo's AIDS patients were HIV positive and they were gays who had used poppers or had inhaled nitrates so there were poisons involved.

Hot oil sexual lubricants with high levels of immune damaging Benzene were almost exclusively sold to gays to coincide with the emergence of AIDS too.

Just rounding up every ill gay man you can find to 'discover' 'the sex virus' that was 'killing' them is appallingly presumptive and bad science to begin with.

Gallo released his findings at a press conference thus turning HIV/AIDS into a Hollywood movie rather than science.

And Gallo also used cord blood to grow his 'retrovirus' samples, cord blood from the placenta being full of retroviruses.

This HIV antibody test was then used to terrorise the gay community, drug users, hemophiliacs, blacks, hispanics, prostitutes and generally anyone they feel like calling 'dirty'.

The CD4 T-cell test was also pulled out of a hat and since being on a low fat diet lowers your T-cell count, starving Africans look as if they have AIDS.

The HIV theory itself is quite blatantly racist. They are still trying to prove that pygmies in the Congo who eat monkey meat somehow got a monkey retrovirus, then had sex with people in cities, who then emigrated to Haiti where gays on sex tours then got 'infected' with a deadly 'sex virus' called HIV.

That is what the HIV/AIDS theory is.

From this basic racist myth, people are sold the slickest drug campaign in history to make them buy the most dubious drugs in history.

Some victims kill themselves on hearing a HIV diagnosis. They spend so much money on AIDS drugs they starve, they get organ damage and immune failure and anemia -and they still believe they are being cured.

The campaign to stop 'HIV' being transmitted from mother to child involves the same doses of AZT that killed Freddie Mercury, Rudolph Nureyev, Kenny Everett and thousands of others before the AZT dose was lowered in 1993.

But women and children get this dose of AZT and Nevirapine for 3 months at least. Women who refuse to drug their children with AZT have them removed or have to fight in court for the right to treat their own children.

Health departments in some African countries now have empty shelves with no painkillers or antibiotics because AIDS drugs blew the budget.

This is the face of AIDS treatment at the end of the marketing campaign. A juggling match of numbers to decide if you've got the right combination to start your drugs.

"Those who have eyes to see are witnessing genocide -- the genocide of gay men. Millions of dollars are now being spent on an international advertising campaign, "Living With HIV, in which gay men and other members of "risk groups" are being told: Get tested for antibodies to HIV -- if you "test positive" you need "medical intervention" which could "put time on your side". The "medical intervention" is AZT (also known as Retrovir and zidovudine), and the campaign is paid for, directly and indirectly, by Burroughs-Wellcome, the manufacturer of AZT."
HIV Voodoo From burroughs Wellcome. John Lauritsen 1991

The problem all along is that no one in the HIV/AIDS industry knew that retroviruses are always in our reproductive organs.

Or if they did know then they failed to mention the fact and continue to stay silent now.

So none of this science has any validity, they are not even qualified if they recommend anti-retrovirals to women while pregnant.

If retroviruses are part and parcel of having breasts, a uterus, cervix and placenta then HIV science jumped the gun and sold us a bunch of tests that mean very little except you could have a few dividing cells if you are a HIV+ guy and or maybe just be pregnant if a woman.

Or simply be a man or woman - the HIV test is that non-specific.

Maybe being HIV+ means you have dog genes???

Well it is a sad joke of a science.

"In a serological survey, using the immunoblotting technique, we found that substantial numbers of dog sera from both normal and diseased dogs, including dogs with neoplasia, reacted with one or more human immunodeficiency virus (HIV) recombinant proteins. A total of 144 dog sera were tested, and 72 (50%) of them reacted with one or more HIV recombinant structural proteins."
Studies with canine sera that contain antibodies which recognize human immunodeficiency virus structural proteins.

So retroviruses always appear in the testes of guys so could be seen as 'sex viruses'.

"The expression of ERVs in male reproductive tissues suggests a possible role in normal and disease conditions involving the testis and epididymis. These speculative functions may include among others spermatogenesis and or sperm maturation or tumour formation. However, further studies need to be carried out to investigate specific roles of ERVs in male reproductive events." 2002
Endogenous retrovirus sequences expressed in male mammalian reproductive tissues: a review.

And retroviruses always appear in the placenta, breasts and cervix of women.

If AIDS scientists get their way then all women, gays, Africans, Hispanics and drug users will be on AIDS drugs and never breeding again so it will be a world left for the rich guys who didn't take a HIV test.

It would be a boring world.

"Retrovirus-like sequences account for 8 to 9% of the human genome."

"In the present study, we have investigated the transcriptional activity of representative members of 20 HERV families in 19 different normal human tissues. Qualitative evaluation of chip hybridization signals and quantitative analysis by real-time RT-PCR revealed distinct HERV activity in the human tissues under investigation, suggesting that HERV elements are active in human cells in a tissue-specific manner. Most active members of HERV families were found in mRNA prepared from skin, thyroid gland, placenta, and tissues of reproductive organs. In contrast, only few active HERVs were detectable in muscle cells."
Comprehensive Analysis of Human Endogenous Retrovirus Transcriptional Activity in Human Tissues with a Retrovirus-Specific Microarray

I don't know how the general public can learn that retroviruses are an every day part of life but they need to know.

Everyone has a responsibility to tell everyone else because everyone takes HIV tests without knowing the danger they face from believing the test and possibly getting convinced to poison themselves with AIDS drugs.

These are problems with the HIV antibody test in their own words so you can decide.

'False-positive HIV serologic screens can be caused by recent influenza vaccination, incidental viral infections, autoimmune disease, renal failure, cystic fibrosis, multiple pregnancies, blood transfusions, liver diseases, parenteral substance abuse, hemodialysis, or vaccinations against hepatitis B and rabies.

- An indeterminate WB result can be caused by a weak titer of anti-HIV-1 antibodies (as seen in early seroconversion), advanced AIDS, infection with an unusual HIV type, or recipients of experimental HIV vaccines. It can also be caused by the presence of antibodies cross-reactive against HIV antigens (incidental viral infection; vaccination against influenza, hepatitis, or rabies; or HTLV infection) or reactivity to the nonviral components of the WB (various autoimmune disorders, multiple pregnancies, and recipients of multiple blood transfusions).

- An increasing number of recipients of experimental HIV vaccines, which can cause false-positive results in HIV serologic tests, are being offered HIV screening. Whenever possible, testing for HIV in such patients is best performed in consultation with the vaccine research group responsible for the trial. This procedure will ensure proper interpretation of test results without compromising the study data.'
Interpretation of HIV Serologic Testing Results

Cal Crilly
Helical Sun