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Originally posted by muzzleflash
One of the difficult parts of this is that when killed, the HIV virus does not elicit an immune response from the body, and so it has to be a live viral sample within the vaccine or it simply won't have any effect at all.
That's what I gathered from reading the source material, if I am misunderstanding antigenicity theory incorrectly anyone can correct me on that.
All corrections are welcomed.
However, the classical vaccination approaches that have been successful in the control of various viral diseases by priming the adaptive immunity to recognize the viral envelope proteins have failed in the case of HIV-1. Some have stated that an HIV vaccine may not be possible without significant theoretical advances.
There are a number of factors that cause development of an HIV vaccine to differ from the development of other classic vaccines:[5]
Classic vaccines mimic natural immunity against reinfection generally seen in individuals recovered from infection; there are almost no recovered AIDS patients.
Most vaccines protect against disease, not against infection; HIV infection may remain latent for long periods before causing AIDS.
Most effective vaccines are whole-killed or live-attenuated organisms; killed HIV-1 does not retain antigenicity and the use of a live retrovirus vaccine raises safety issues.
Most vaccines protect against infections that are infrequently encountered; HIV may be encountered daily by individuals at high risk.
Most vaccines protect against infections through mucosal surfaces of the respiratory or gastrointestinal tract; the great majority of HIV infection is through the genital tract.
A. S. Fauci, 1996, An HIV vaccine: breaking the paradigms, Proc. Am. Assoc. Phys. 108:6.
It is from this frame of reference that I present to you the vaccine fraud. Vaccines today are a sacred (cash) cow, a modern medical "miracle" without which we'd all be crippled, dead, or worse. Anyone who suggests they might be the cause of autism, ADD, ADHD, Alzheimer's, and a plethora of auto-immune disorders is annihilated by the establishment.
At this point you may be trying to rationalize the whole thing, something along the lines of, just because they dump fluoride in our water doesn't mean the vaccines are bad. No, of course not. But if they'd dump sodium fluoride in our water, it shouldn't be beyond the realm of possibility that they've completely lied about the vaccines. And lie they have.
Vaccine ingredients contain what can reasonably be described as a Nazi experiment, including mercury, aluminum, ethylene glycol (anti-freeze), chemical detergents, formaldehyde, foreign recombinant RNA including aborted fetal retinal tissue and cancer cells from monkeys, and poly-sorbate 80, or preen 80, a known sterilant – all entering your body in an unnatural fashion (injection) for which your body has little ability to defend against. If this seems absurd to you, compare this list to any vaccine insert, if you can convince a pharmacist to actually let you look at one.
Particularly in children, who have weakened blood-brain barriers, these toxic substances, including violent neurotoxins (which, in the case of mercury, have recently been declared by establishment medicine, reported by establishment media, as beneficial to children with developing brains), wreak havoc on the brain, and often overheat the immune system causing violent autoimmune responses (such as vaccine induced encephalitis (“shaken baby syndrome”)) and immune disorders that make them pharma clients for life.
The whole concept of vaccination was developed by Edward Jenner, an 18th century English doctor who based his entire theory on an old wives' tale that people who came down with cowpox were somehow immune to smallpox. Testing this theory in May of 1796, he removed fluid from a woman's cowpox lesion and injected it into the arm of a healthy 8 year old boy. Jenner then later injected the boy with smallpox. When the boy did not get smallpox, Jenner concluded, "The cowpox protects the human constitution from the infection of smallpox." That's it. That's what the entire science is based on - this wholly unscientific test.
Common sense tells us that not everyone who ever came into contact with smallpox became symptomatic, else the overwhelming majority of humanity would've been afflicted. Jenner's finding was published in 6 languages and, again, is the basis for an entire industry of vaccine producing pharmaceutical companies who reap in billions off it.
Is it not, therefore, rather strange, Mr. President, that vaccination should be reported as so utterly harmless in the distant Philippines, where we can not easily get at the records, when we know it is so deadly in the nearby England and America, where the accessible records show that it causes, frequently, more deaths than smallpox, as I have already proved? For example: the great English Commission on Vaccination found that deaths from vaccination were sometimes as high as seventy deaths per million vaccinated. This is twice as high as the mortality from smallpox in the United States, which for five years, from 1901 to 1905, including our last great epidemic period of 1901 and 1902, averaged only thirty-four deaths per million population! - Charles M Higgins
Originally posted by FissionSurplus
In a nutshell, hell NO.
First the government invents this monster (US Army Patent #5242820), then they let their Big Pharma friends try and make a vaccine for it.
If they don't kill you, they want to make money off you.
Researchers believe the game-changing technology could substantially accelerate synthetic biology research and development, leading to everything from the creation of new food sources to the growth of new organs for transplant patients.
“We are looking at creating a cell’s equivalent to a computer operating system in such a way that a given group of cells could be seamlessly re-programmed to perform any function without needing to modify its hardware,” says Natalio Krasnogor, professor of computer science at the University of Nottingham.
“We are talking about a highly ambitious goal leading to a fundamental breakthrough that will, ultimately, allow us to rapidly prototype, implement, and deploy living entities that are completely new and do not appear in nature, adapting them so they perform new useful functions.”
The project called Towards a Biological Cell Operating System (AUdACiOuS) is attempting to go beyond systems biology—the science behind understanding how living organisms work—to give scientists the power to create biological systems.
Part of the funding for the facility will come from the Bill and Melinda Gates Foundation.
II- CREATION OF THE MYCOPLASMA
A Laboratory-Made Disease Agent Many doctors don’t know about this mycoplasma disease agent because it was developed by the US military in biological warfare experimentation and it was not made public. This pathogen was patented by the United States military and Dr Shyh-Ching Lo. I have a copy of the documented patent from the US Patent Office.
(1) All the countries at war were experimenting with biological weapons. In 1942, the governments of the United States, Canada and Britain entered into a secret agreement to create two types of biological weapons (one that would kill, and one that was disabling) for use in the war against Germany and Japan, who were also developing biological weapons. While they researched a number or disease pathogens, they primarily focused on the Brucella bacterium and began to weaponise it.
From its inception, the biowarfare program was characterised by continuing in-depth review and participation by the most eminent scientists, medical consultants, industrial experts and government officials, and it was classified Top Secret.
The US Public Health Service also closely followed the progress of biological warfare research and development from the very start of the program, and the Centers for Disease Control (CDC) and the National Institutes of Health (NIH) in the United States were working with the military in weaponising these diseases. These are diseases that have existed for thousands of years, but they have been weaponised—which means they’ve been made more contagious and more effective. And they are spreading.
The Special Virus Cancer Program, created by the CIA and NIH to develop a deadly pathogen for which humanity had no natural immunity (AIDS), was disguised as a war on cancer but was actually part of MKNAOMI.2 Many members of the Senate and House of Representatives do not know what has been going on. For example, the US Senate Committee on Government Reform had searched the archives in Washington and other places for the document titled "The Special Virus Cancer Program: Progress Report No. 8", and couldn’t find it. Somehow they heard I had it, called me and asked me to mail it to them. Imagine: a retired schoolteacher being called by the United States Senate and asked for one of their secret documents! The US Senate, through the Government Reform Committee, is trying to stop this type of government research.
Crystalline Brucella
The title page of a genuine US Senate Study, declassified on February 24, 1977, shows that George Merck, of the pharmaceutical company, Merck Sharp & Dohme (which now makes cures for diseases that at one time it created), reported in 1946 to the US Secretary of War that his researchers had managed "for the first time" to "isolate the disease agent in crystalline form".3
Source
The study was carried out by the US army and the Thai government over seven years on volunteers - all HIV-negative men and women aged between 18 and 30 - in parts of Thailand.
Half of the volunteers were given the vaccine, while the other half were given a placebo - and all were given counselling on HIV/Aids prevention.
Participants were tested for HIV infection every six months for three years.
The results found that the chances of catching HIV were 31.2% less for those who had taken the vaccine - with 74 people who did not get the vaccine infected and 51 of the vaccinated group infected.
The vaccine is based on B and E strains of HIV that most commonly circulate in Thailand not the C strain which predominates in Africa. The vaccine was a combination of two older vaccines that on their own had not cut infection rates.
III — COVERT TESTING OF MYCOPLASMA Testing the Dispersal Methods Documented evidence proves that the biological weapons they were developing were tested on the public in various communities without their knowledge or consent.
The government knew that crystalline Brucella would cause disease in humans. Now they needed to determine how it would spread and the best way to disperse it. They tested dispersal methods for Brucella suis and Brucella melitensis at Dugway Proving Ground, Utah, in June and September 1952. Probably, 100% of us now are infected with Brucella suis and Brucella melitensis.(8)
Another government document recommended the genesis of open-air vulnerability tests and covert research and development programs to be conducted by the Army and supported by the Central Intelligence Agency. At that time, the Government of Canada was asked by the US Government to cooperate in testing weaponised Brucella, and Canada cooperated fully with the United States.
The US Government wanted to determine whether mosquitoes would carry the disease and also if the air would carry it. A government report stated that "open-air testing of infectious biological agents is considered essential to an ultimate understanding of biological warfare potentialities because of the many unknown factors affecting the degradation of micro-organisms in the atmosphere".9
Testing via Mosquito Vector in Punta Gorda, Florida A report from The New England Journal of Medicine reveals that one of the first outbreaks of chronic fatigue syndrome was in Punta Gorda, Florida, back in 1957.(10)
It was a strange coincidence that a week before these people came down with chronic fatigue syndrome, there was a huge influx of mosquitoes.
The National Institutes of Health claimed that the mosquitoes came from a forest fire 30 miles away. The truth is that those mosquitoes were infected in Canada by Dr Guilford B. Reed at Queen’s University. They were bred in Belleville, Ontario, and taken down to Punta Gorda and released there.
Within a week, the first five cases ever of chronic fatigue syndrome were reported to the local clinic in Punta Gorda. The cases kept coming until finally 450 people were ill with the disease. Testing via Mosquito Vector in Ontario The Government of Canada had established the Dominion Parasite Laboratory in Belleville, Ontario, where it raised 100 million mosquitoes a month.
These were shipped to Queen’s University and certain other facilities to be infected with this crystalline disease agent The mosquitoes were then let loose in certain communities in the middle of the night, so that the researchers could determine how many people would become ill with chronic fatigue syndrome or fibromyalgia, which was the first disease to show.
One of the communities they tested it on was the St Lawrence Seaway valley, all the way from Kingston to Cornwall, in 1984. They let out hundreds of millions of infected mosquitoes. Over 700 people in the next four or five weeks developed myalgic encephalomyelitis, or chronic fatigue syndrome.
The purpose of this study was to design novel nanocapsules (NCs) with surface-chelated nickel (Ni-NCs) as a vaccine delivery system for histidine (His)-tagged protein antigens.
Notably, sera and vaginal secretions from HIV-1(IIIB) VLP-CCL28-treated mice exhibited an enhanced neutralizing activity against both a HIV-1/B-subtype laboratory strain and a heterologous HIV-1/C-subtype primary isolate. These data suggest that CCL28 could be useful in enhancing the IgA immune response that will likely play a pivotal role in prophylactic HIV vaccines.
Originally posted by Heyyo_yoyo
Actually....
Since I mentioned that I'd never vaccinate again, here is one major reason why:
Dr. Bob Beck - Blood Electrification/ Colloidal Silver immunization
Read up on it, plus get access to a two hour video with Dr. Beck lecturing at U.C. Berkley on the Patent he discovered that lead to his development of a viable biological cleansing system, in the ATS thread entitled:
A real CURE for AIDS, Hepatitis, Cancer, Herpes etc, for less than the price of a night out!
archives, out!
infected blood on the insect's mouthparts might be carried to another host while the blood is still fresh and the virus is still alive. Infection by this means is possible but highly unlikely....
Originally posted by DerepentLEstranger
reply to post by popsmayhem
LL guess you won't be vaccinating your kids against aids then, you'd have to wait 10-20 yrs to be absolutely sure.
the "normal" incubation period of is 10 yrs but it may have been modified to increase incubation period so as to get another batch of victims 10 yrs later.
10 yrs later:
big pharma: "see! 10 yrs have gone by and nobody has aids, let no one continue to repeat the lies of the CTs!"
15 yrs later:
MSM: scientists at CDC continue to be baffled by what seems to be a massive outbreak throughout the world of what some have begun to call Super AIDS...
Vaccines: Pre-Industrial Age Quackery Posing As Modern Science: gnosis474.blogspot.com...
It is from this frame of reference that I present to you the vaccine fraud. Vaccines today are a sacred (cash) cow, a modern medical "miracle" without which we'd all be crippled, dead, or worse. Anyone who suggests they might be the cause of autism, ADD, ADHD, Alzheimer's, and a plethora of auto-immune disorders is annihilated by the establishment.
At this point you may be trying to rationalize the whole thing, something along the lines of, just because they dump fluoride in our water doesn't mean the vaccines are bad. No, of course not. But if they'd dump sodium fluoride in our water, it shouldn't be beyond the realm of possibility that they've completely lied about the vaccines. And lie they have.
Vaccine ingredients contain what can reasonably be described as a Nazi experiment, including mercury, aluminum, ethylene glycol (anti-freeze), chemical detergents, formaldehyde, foreign recombinant RNA including aborted fetal retinal tissue and cancer cells from monkeys, and poly-sorbate 80, or preen 80, a known sterilant – all entering your body in an unnatural fashion (injection) for which your body has little ability to defend against. If this seems absurd to you, compare this list to any vaccine insert, if you can convince a pharmacist to actually let you look at one.
Particularly in children, who have weakened blood-brain barriers, these toxic substances, including violent neurotoxins (which, in the case of mercury, have recently been declared by establishment medicine, reported by establishment media, as beneficial to children with developing brains), wreak havoc on the brain, and often overheat the immune system causing violent autoimmune responses (such as vaccine induced encephalitis (“shaken baby syndrome”)) and immune disorders that make them pharma clients for life.
The whole concept of vaccination was developed by Edward Jenner, an 18th century English doctor who based his entire theory on an old wives' tale that people who came down with cowpox were somehow immune to smallpox. Testing this theory in May of 1796, he removed fluid from a woman's cowpox lesion and injected it into the arm of a healthy 8 year old boy. Jenner then later injected the boy with smallpox. When the boy did not get smallpox, Jenner concluded, "The cowpox protects the human constitution from the infection of smallpox." That's it. That's what the entire science is based on - this wholly unscientific test.
Common sense tells us that not everyone who ever came into contact with smallpox became symptomatic, else the overwhelming majority of humanity would've been afflicted. Jenner's finding was published in 6 languages and, again, is the basis for an entire industry of vaccine producing pharmaceutical companies who reap in billions off it.
Is it not, therefore, rather strange, Mr. President, that vaccination should be reported as so utterly harmless in the distant Philippines, where we can not easily get at the records, when we know it is so deadly in the nearby England and America, where the accessible records show that it causes, frequently, more deaths than smallpox, as I have already proved? For example: the great English Commission on Vaccination found that deaths from vaccination were sometimes as high as seventy deaths per million vaccinated. This is twice as high as the mortality from smallpox in the United States, which for five years, from 1901 to 1905, including our last great epidemic period of 1901 and 1902, averaged only thirty-four deaths per million population! - Charles M Higgins