by Jon Rappoport
June 13, 2022
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(This article is Part-4 in a series. For Part-3, click here.)
This is another article in which I assume, for the purposes of argument only, that virologists are actually discovering viruses, and vaccines are launched to prevent viral diseases.
Why do I bother? Because most people belong to the virus religion. They have faith. They pray at the altar of the virus.
OK. What is the role of antibodies in vaccines?
We’re told that the vaccine produces a beneficial antibody response. These antibody scouts of the immune system rush to the scene and identify the injected viruses or parts of viruses—thereby alerting the foot soldiers of the immune system, which march forward and destroy/neutralize the viral components.
Thus, vaccination is a rehearsal for the real thing. It prepares the body for the later moment when the virus naturally shows up. The body is ready to defeat the actual disease.
In my previous article on that subject, I showed the rehearsal is a farce. It doesn’t prepare the immune system for anything.
The so-called adjuvants in the vaccine, which are supposed to enhance and magnify the immune response, simply stimulate a reaction against themselves, the adjuvants.
Now, I’m going further.
Below, I’m going to republish an excerpt from a devastating Christine Johnson article which shows the failure of the HIV antibody test.
Johnson’s article proves that antibodies, which are supposed to be specific to HIV and only HIV, meaning they only swing into action when HIV appears, are responding to all sorts of substances in the body, none of which has anything to do with HIV.
This means the antibodies aren’t “specific.” They aren’t just marching to one tune. They’re marching to many different tunes.
In the case of vaccination, antibodies can appear because: there are intrusive non-viral substances in the vaccine; or there are intrusive non-viral substances already in the body.
Defenders of vaccination might respond, “Suppose antibodies are responding to six different factors in the vaccine. One of those factors would be the virus in the vaccine. So that’s good.”
BUT if antibodies are really general and not specific, how do we know they actually react to a virus in a vaccine and not something else in the vaccine or the body?
We don’t know.
We’re looking at false science, science without a punch line.
Here is an excerpt from the 1996 Christine Johnson article on the HIV blood test — with the corresponding reference number(s) to the scientific literature:
Factors Known to Cause False-Positive HIV Antibody Test Results:
* Anti-carbohydrate antibodies (52, 19, 13)
* Naturally-occurring antibodies (5, 19)
* Passive immunization: receipt of gamma globulin or immune globulin (as prophylaxis against infection which contains antibodies)(18, 26, 60, 4, 22, 42, 43, 13)
* Leprosy (2, 25)
* Tuberculosis (25)
* Mycobacterium avium (25)
* Systemic lupus erythematosus (15, 23)
* Renal (kidney) failure (48, 23, 13)
* Hemodialysis/renal failure (56, 16, 41, 10, 49)
* Alpha interferon therapy in hemodialysis patients (54)
* Flu (36)
* Flu vaccination (30, 11, 3, 20, 13, 43)
* Herpes simplex I (27)
* Herpes simplex II (11)
* Upper respiratory tract infection (cold or flu)(11)
* Recent viral infection or exposure to viral vaccines (11)
* Pregnancy in multiparous women (58, 53, 13, 43, 36)
* Malaria (6, 12)
* High levels of circulating immune complexes (6, 33)
* Hypergammaglobulinemia (high levels of antibodies) (40, 33)
* False positives on other tests, including RPR (rapid plasma reagent) test for syphilis (17, 48, 33, 10, 49)
* Rheumatoid arthritis (36)
* Hepatitis B vaccination (28, 21, 40, 43)
* Tetanus vaccination (40)
* Organ transplantation (1, 36)
* Renal transplantation (35, 9, 48, 13, 56)
* Anti-lymphocyte antibodies (56, 31)
* Anti-collagen antibodies (found in gay men, haemophiliacs, Africans of both sexes and people with leprosy)(31)
* Serum-positive for rheumatoid factor, antinuclear antibody (both found in rheumatoid arthritis and other autoantibodies)(14, 62, 53)
* Autoimmune diseases (44, 29, 10, 40, 49, 43): Systemic lupus erythematosus, scleroderma, connective tissue disease, dermatomyositis
* Acute viral infections, DNA viral infections (59, 48, 43, 53, 40, 13)
* Malignant neoplasms (cancers)(40)
* Alcoholic hepatitis/alcoholic liver disease (32, 48, 40,10,13, 49, 43, 53)
* Primary sclerosing cholangitis (48, 53)
* Hepatitis (54)
* “Sticky” blood (in Africans) (38, 34, 40)
* Antibodies with a high affinity for polystyrene (used in the test kits)(62, 40, 3)
* Blood transfusions, multiple blood transfusions (63, 36,13, 49, 43, 41)
* Multiple myeloma (10, 43, 53)
* HLA antibodies (to Class I and II leukocyte antigens)(7, 46, 63, 48, 10, 13, 49, 43, 53)
* Anti-smooth muscle antibody (48)
* Anti-parietal cell antibody (48)
* Anti-hepatitis A IgM (antibody)(48)
* Anti-Hbc IgM (48)
* Administration of human immunoglobulin preparations pooled before 1985 (10)
* Haemophilia (10, 49)
* Haematologic malignant disorders/lymphoma (43, 53, 9, 48, 13)
* Primary biliary cirrhosis (43, 53, 13, 48)
* Stevens-Johnson syndrome9, (48, 13)
* Q-fever with associated hepatitis (61)
* Heat-treated specimens (51, 57, 24, 49, 48)
* Lipemic serum (blood with high levels of fat or lipids)(49)
* Haemolyzed serum (blood where haemoglobin is separated from the red cells)(49)
* Hyperbilirubinemia (10, 13)
* Globulins produced during polyclonal gammopathies (which are seen in AIDS risk groups)(10, 13, 48)
* Healthy individuals as a result of poorly-understood cross-reactions (10)
* Normal human ribonucleoproteins (48,13)
* Other retroviruses (8, 55, 14, 48, 13)
* Anti-mitochondrial antibodies (48, 13)
* Anti-nuclear antibodies (48, 13, 53)
* Anti-microsomal antibodies (34)
* T-cell leukocyte antigen antibodies (48, 13)
* Proteins on the filter paper (13)
* Epstein-Barr virus (37)
* Visceral leishmaniasis (45)
* Receptive anal sex (39, 64)
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Jon Rappoport
The author of three explosive collections, THE MATRIX REVEALED, EXIT FROM THE MATRIX, and POWER OUTSIDE THE MATRIX, Jon was a candidate for a US Congressional seat in the 29th District of California. He maintains a consulting practice for private clients, the purpose of which is the expansion of personal creative power. Nominated for a Pulitzer Prize, he has worked as an investigative reporter for 30 years, writing articles on politics, medicine, and health for CBS Healthwatch, LA Weekly, Spin Magazine, Stern, and other newspapers and magazines in the US and Europe. Jon has delivered lectures and seminars on global politics, health, logic, and creative power to audiences around the world. You can sign up for his free NoMoreFakeNews emails here or his free OutsideTheRealityMachine emails here.
