Bedrock of vaccination theory crumbles as science reveals antibodies not necessary to fight viruses

by Ethan A. Huff, staff writer

http://www.naturalnews.com/z035371_vaccine_theory_antibodies_viruses.html

march 2012

While the medical, pharmaceutical, and vaccine industries are busy pushing new vaccines for practically every condition under the sun, a new study published in the journal Immunity completely deconstructs the entire vaccination theory. It turns out that the body’s natural immune systems, comprised of both innate and adaptive components, work together to ward off disease without the need for antibody-producing vaccines.

The theory behind vaccines is that they mimic infection by spurring B cells, one of the two major types of white blood cells in the immune system, to produce antibodies as part of the adaptive immune system. It is widely believed that these vaccine-induced antibodies, which are part of the more specific adaptive immune system, teach the immune system how to directly respond to an infection before the body becomes exposed to it.

But the new research highlights the fact that innate immunity plays a significant role in fighting infections, and is perhaps more important than adaptive immunity at preventing or fighting infections. In tests, adaptive immune system antibodies were shown unable to fight infection by themselves, which in essence debunks the theory that vaccine-induced antibodies serve any legitimate function in preventing or fighting off infection.

“Our findings contradict the current view that antibodies are absolutely required to survive infection with viruses like VSV (vesicular stomatitis virus), and establish an unexpected function for B cells as custodians of macrophages in antiviral immunity,” said Dr. Uldrich H. von Andrian from Harvard Medical School. “It will be important to further dissect the role of antibodies and interferons in immunity against similar viruses that attack the nervous system, such as rabies, West Nile virus, and Encephalitis.”

As explained by Dr. Russell Blaylock in a recent interview with Mike Adams, the Health Ranger, vaccines not only do not work as advertised, but they actually damage the body’s innate immunity. Rather than teach the body how to respond to infections, vaccines actually inhibit the immune system’s ability to produce TH2-type cytokines, and suppress cellular immunity, which is how the body protects itself against deadly viruses and bacteria.

So once again, the myth that vaccinations serve any sort of legitimate medical purpose has been deconstructed by breakthrough science. Regardless of whether or not the mainstream medical community wants to admit it, pro-vaccine ideology is increasingly finding itself in the dustheap of outmoded pseudoscience.

Sources for this article include:

http://www.medicalnewstoday.com/releases/242403.php

http://www.niaid.nih.gov

http://www.naturalnews.com/035335_vaccines_Dr_Blaylock_children.html

…bless you all…

Disease Caused by Vaccines

When people are subject to repeated vaccines, they predictably simulate a situation of suppressed cell-mediated immunity and heightened antibody responses. Why? Because that’s the goal of vaccination. If you make a list of the diseases that are characterized by suppressed cell-mediated immunity and heightened humoral immunity, you’re talking health conditions like asthma, allergies, eczema and autoimmune diseases including Crohn’s, Vitiligo, Multiple Sclerosis, Sjogren’s syndrome, Hashimoto’s, etcetera.
We cannot and will not eradicate all disease with vaccines. We have merely traded acute illnesses from which most recover for chronic illnesses for which modern medicine has no cure.
Ask your grandparents or parents how many children did they know in 1940’s or ’50’s who had allergies, and the answer is basically none. Now, it’s anywhere from 20 to 40% of children have some sort of chronic illness.
Fifteen percent of children suffer from asthma. (1) Something is wrong with this picture.
So how did we get here? Many of today’s chronic diseases are characterized by excessive antibody production.
How did we get that? Well that was the point of the vaccination program. That’s the goal. Why would you expect anything else to happen? Many of you may respond, “This has never been proven.”
Actually, the fact that vaccines produce more illness has been proven. Longitudinal survey studies comparing the health of vaccinated versus unvaccinated children have repeatedly shown statistically significant vaccinosis – illness produced in an individual after receiving a vaccine. In a 1997 study in New Zealand, 1265 children were surveyed. Twenty-three percent of the vaccinated children experienced asthma and thirty percent suffered from allergies, while the unvaccinated children did not have a single incident of these illnesses. (2) In a 2004 British
Study of 30,000 children, vaccinated children had a 5.04 increased risk of asthma, while the unvaccinated only had a .36 percent prevalence. (3) In a 2011 German Study of 8000 children, vaccinated children had at least two to five times more diseases and disorders than unvaccinated children.
In patients with an autoimmune disorder, the immune system can’t tell the difference between healthy body tissue and antigens that need to be attacked. The result is an immune response that destroys normal body tissues. This response is a hypersensitivity reaction similar to the response in allergic conditions. Vaccinations have been shown to induce autoimmune disorders.
Interestingly, there’s a study out of Kobe University in Japan where they took mice and put them on a rigorous
vaccination program. They wanted to see if they could develop excessive antibodies as seen in autoimmune disease. And they found that at a certain threshold they could consistently and reliably induce autoimmune disease by simply giving enough vaccinations. (4)
The Kobe University study authors concluded:

Systemic autoimmunity appears to be the inevitable consequence of over-stimulating the host’s
immune ‘system’ by repeated immunization with antigen to the levels that surpass the system’s
self-organize criticality.

In other words, they found that, not only is vaccination a possible or even probable cause of autoimmune disorders, but that chronic diseases are the inevitable result of vaccinations!
This study was done with mice. This begs the question, ‘Has this been replicated in humans?’ Unequivocally yes. This experiment has been done and it’s called the last 70 years.
Autoimmune diseases have increased in quantity and variety as the number of vaccinations has increased over the last 70 years. There are over 100 autoimmune diseases. Studies with monogenetic twins have revealed that genetic influences only account for 25–40% of the disease risk making environmental influences the predominant factors. (5) Regardless of genetic vulnerability, one’s environment determines whether genes for autoimmunity are expressed.
There is a reason the fastest growing subset of diseases in the US and the world are autoimmune diseases. This is because we’re producing them. It’s a growth industry. As vaccines have increased in number, so have the number of cases of autoimmune disease.
Currently, there are 38 vaccines on the recommended schedule, with even more in some US states. There are many more vaccines in development. I predict a worsening epidemic of allergies, asthma, autoimmune and other diseases caused by an atrophy of the cell-mediated immune response as more vaccines are added to the vaccine schedule. We are only seeing the tip of the iceberg with vaccine-induced disease.

  1. Channick, R. More Astham Inhalers going to School: New State Law Eliminates Need to Doctor’s Written Permission. Chicago Tribune. October 1, 2012.
  2. 6 Kemp, T et al. Is Infant Immunization a Risk Factor for Childhood Asthma or Allergy? Epidemiology. 1997 Nov 8: 678-80. http://www.ncbi.nlm.nih.gov/pubmed/9345669
  3. 8 McKeever TM et al. Vaccination and Allergic Disease: A Birth Cohort Study. American Journal of Public Health. June 2004, Vol 94, No. 6, pp 985-989. http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1448377/
  4. 11 Novaccine.com. Reactions/Conditions. http://www.novaccine.com/reactions-conditions/
  5. Karopka, T, Fluck, J, Mevissen, H, Glass, A.  The Autoimmune Disease Database: a dynamically compiled literature-derived database. BMC Bioinformatics 2006, 7:325  doi:10.1186/1471-2105-7-325. http://www.biomedcentral.com/1471-2105/7/325

    …bless you all…

Inducing Antibodies does not produce immunity

http://www.jabs.org.uk/forum/topic.asp?TOPIC_ID=1391

Scientists have known at least since 1940 that the primitive concept of simply inducing antibodies does not produce immunity. The immune system is much more complex than they thought. They now know that it consists of at least two parts; the humoral and the cellular. If one is activated the other is suppressed. This was not known when vaccination first was introduced. In view of this more recent knowledge their approach has been to try and prevent the suppression, with some ghastly outcomes. If you recall the Phase I trial of TeGenero’s TGN1412 experiment last year that went horribly wrong and five young volunteers nearly died – that was a drug designed to prevent suppression of cellular immune function. When will we learn to stop playing God with the immune system, which is far more intelligent than any scientist.

In view of this knowledge it surprises me that it is still claimed vaccination produces immunity.

The following is an extract from the website of Dr Rebecca Carly who explains it much better.

“DR Rebecca Carley

What this author has realized is that bypassing this mucosal aspect of the immune system by directly injecting organisms into the body leads to a corruption in the immune system itself whereby IgA is transmuted into IgE, and/or the B cells are hyperactivated to produce pathologic amounts of self-attacking antibody as well as suppression of cytotoxic T cells

“stealth adapted”. These are formed when vaccine viruses combine with viruses from tissues used to culture them, or when bacteria lose their cell walls when a person takes antibiotics and transform into “L forms”, leading to a lack of some critical antigens normally recognized by the cellular immune system. Another example is stealth adapted (mutated) cytomegaloviruses which arose from African green monkey (simian) kidney cells when they were used to culture polio virus for live polio virus vaccines. Thus, not only was the vaccinee inoculated with polio, but with the cytomegalovirus as well.

The mechanism by which the immune system is corrupted can best be realized when you understand that the two poles of the immune system (the cellular and humoral mechanisms) have a reciprocal relationship in that when the activity of one pole is increased, the other must decrease. Thus, when one is stimulated, the other is inhibited. Since vaccines activate the B cells to secrete antibody, the cytotoxic (killer) T cells are subsequently suppressed.

In fact, the “prevention” of a disease via vaccination is, in reality, an inability to expel organisms due to the suppression of the cell-mediated response. Thus, rather than preventing disease, the disease is actually prevented from ever being resolved.

Thus, the autoimmune disease you develop is determined by which tissues in the body are attacked by auto antibodies. If the inside lining of the gastrointestinal tract (the mucosa) is attacked by auto-antibodies you develop leaky gut syndrome

Crohn’s disease and colitis are also caused by auto-antibody attack on the mucosa of the GI tract itself.

If the islet (insulin producing) cells of the pancreas are attacked by auto-antibodies, you develop insulin dependent (juvenile) diabetes

. If the respiratory mucosa is attacked by auto-antibodies, you develop “leaky lung” syndrome where, just as with leaky gut, antigens recognized as foreign to the body which are inhaled are able to traverse the lining of the respiratory tract, causing the creation of antibodies against those antigens (usually dust, mold, pet or pollen antigens).

If the components of the articular surface of the joints are attacked by auto-antibodies, you develop rheumatoid (or juvenile) arthritis.

If the kidney tissue is attacked by auto-antibodies, you develop one of the many types of nephritis,

If you develop auto-antibodies against the very DNA in the nucleus of all cells, you develop systemic Lupus (thus, the autoimmune potential of DNA vaccines being developed now is self evident; worse yet, DNA components from these vaccines can be incorporated into your DNA, leading to actual genetic changes which could cause extinction of all (vaccinated) life on the Earth, as will be discussed shortly). And on, and on, and on.

The brain and spinal cord can also be attacked with auto-antibodies (which this author refers to as vaccine induced encephalitis), leading to a variety of neurological diseases. The most severe of these, leading to death, are sudden infant death syndrome (SIDS) and most cases of “shaken baby syndrome”

If components of the myelin sheath (the insulating covering of nerve fibers which allows proper nerve conduction) or the actual neurofilaments themselves are attacked by auto-antibodies, the resultant condition is determined solely by the location of the damage done. Such neurological conditions include but are not limited to minimal brain dysfunction, ADD/ADHD, learning disabilities, mental retardation, criminal behavior, the spectrum of pervasive developmental disorders (including autism), multiple sclerosis, Parkinson’s disease, Lou Gehrig’s disease, Guillen Barre’, seizure disorders,

Molecular mimicry is due to similarity of proteins contained in organisms and mammals. (For example, the measles virus is made up of proteins similar to myelin basic protein; thus, antibodies formed against the measles virus antigens subsequently also cause an auto-antibody attack against myelin basic protein in the myelin sheath due to cross reactivity of these antibodies).”

…bless you all…

Our Immune System – Hands Down – How It Works!

 Allow me to illustrate exactly how vaccines throw our immune systems off track. Humans have two different arms of our immune system. One is called cell-mediated immunity and the other is called humoral immunity. During the normal course of an infection, both arms of the immune system are involved. Let’s take the chickenpox virus as an example. You get infected with the virus. Then you make a cell-mediated reaction and are sick for 2 weeks. Then your humoral immunity kicks in and you make antibodies so that if you are ever exposed to the chickenpox again, you will tag it and your immune system will destroy it before it infects your cells and you won’t become sick. That’s how the immune system works – both aspects are always involved.

Cell-mediated Immunity

Cell-mediated immunity entails the system of white blood cells that attack if you unfortunately pick up a virus. And because you’ve never encountered this virus before, the virus will infect, or get inside, different bodily cells. For instance, it will infect the cells of your respiratory tract. Now your white blood cells attack these infected cells and kill them. This whole process releases substances called cytokines, which produce the ill affects you feel when you get sick.

What we call being sick – fever, flu, mucus, cough, rash, etcetera is because of our cell-mediated immune system. The virus does not create the symptoms you experience; they are compliments of your immune system. This is demonstrated clearly when you suppress somebody’s cell-mediated immune system with steroid drugs like prednisone and then infect them with a virus. They don’t get ‘sick.’ They might even die from the infection, but they won’t get what we normally refer to as sick. On the other hand, if you give somebody the chemicals (cytokines, etc.) of their cell-mediated system, you can stimulate a cell-mediated immune response without any infection at all – no virus, no bacteria, no nothing. You merely stimulate their cell-mediated immune system and they get sick. They have a cough, fever, rash and mucus and all the rest. So that which we call being sick is a cell-mediated response.

You may not want to go around boasting how you never get sick. This is very likely because your cell-mediated immunity is repressed so that you don’t release cytokines and then suffer with colds and flus. However, this doesn’t mean that you don’t have these viruses in your body causing harm. It just means your immune system and body are too depleted, overwhelmed and tired to respond.

This is exactly what is happening when individuals receive too many vaccinations, which at some point represses their cell-mediated immunity and their body’s ability to respond to new invaders. They then become susceptible to countless diseases.

Humoral Immunity

 After your cell-mediated immune system clears a pathogen, your humoral immunity – the antibody system – remembers what happened. In about 4 to 6 weeks you have your very own immunity to the pathogen in question. Next time you are exposed to the same pathogen, you can manufacture antibodies in your defense.

You clear the cold before it infects your cells. The cell-mediated immune system never needs to get involved and you don’t get sick.

There has never been until the 1940’s a situation where you have the stimulation of one part of the immune system without the other. That’s what happens with vaccines – the whole point of a vaccine is to stimulate the humoral immunity. The humoral antibodies are stimulated without a prior cell-mediated response.

This type of unnatural stimulation of our immune system is unprecedented. When you get the chickenpox vaccine, the whole point is to stimulate antibodies. If a vaccine stimulated a cell-mediated response, parents would likely not be as motivated to get their kids vaccinated. So, by definition, a vaccination program is the attempt to stimulate the antibodies without a cell-mediated response.

…bless you all…