How vaccines destroy inherent immunity.
TH1 & TH2; How vaccines destroy inherent immunity.
- Compiled by Martinez Sabrina.
A balance of Th1/Th2 cells in the
body is defined as immunostasis (or immune balance) and is required for optimum
health and wellness. Vaccines promote a failure in immunostasis by making the
Th2-type cells dominant.
In Natural Immunity, for example
exposure to chickenpox, Th1 response externalizes the infection and provides
permanent immunity.
In Vaccine-Induced Immunity, Th2 response internalizes the infection because the Immune System was forced into an emergency -based Th2 response and results in poor immune memory. Thus regular vaccine boosters are required throughout life.
T cells (thymus cells) are the
major cell in the immune system; they direct and control all immune responses
as well as immune memory. Subsets of T cells are the T-helper cells (Th).
T-helper cells coordinate and direct the safest and most effective immune
response. Using Moskowitz’s measles example, we know that, when infected with
the measles virus naturally via the nasopharyngeal route, the body produces a
Th1 response that externalizes the infection and provides permanent immunity.
Fever, rash, coughing, sneezing, etc are signs of the body ridding itself of
this infection. Bypassing the normal body lines of defense by injecting a
vaccine forces the immune system into an emergency-based Th2 response which
serves to internalize the infection. You don’t get the disease but are
susceptible to the disease later since the Th2 response results in poor immune
memory. So, if a natural, viral (measles) infection results in a Th1 response,
why don’t we make vaccines that could elicit the same response.
Adjuvants are often employed to
enhance the development of an efficacious specific response. The problem lies
within what type of immune response is happening. TH1 is the cell-mediated
immune response that happens after naturally acquiring an infection, and then
TH2 humoral kicks in with antibodies and ensures immunity, but, they work in
tandom. Vaccination uses adjuvants to stimulate a TH2 response, bypassing the
TH1, which puts the immune system into a perpetual state of confusion. This can
kick in Autoimmunity for predisposed individuals (See the medical textbook
“Vaccines and Autoimmunity” by world renowned immunologist Dr. Yehuda Shoenfeld
MD).
The vaccination process itself
destroys immune capacity by overstimulating the humoral TH2 immune response
while never engaging the cell-mediated TH1 immune response. The immune system
then stays in a state of agitation, which leads to all sorts of chronic health
problems, injury and death. And, never confers immunity (e.g., booster shots
are required to create more antibodies - the only measurement of "vaccine
effectiveness"). On the other hand, when a child naturally gets an infection
a proper TH1 immune response occurs, and then TH2 kicks in, tags the antigens
with antibodies and we now have immunity. No need for booster shots.
"What people don't know
about vaccines --what most doctors don't know-- but well demonstrated in medical
literature, is that vaccines shift your immune system to an immune suppression
type of state called the "TH2 shift." That's what most vaccines do.
They shift your immune system to a weaker, antibody type immune system... If
you're injecting people with so many vaccines that your keeping them in this
constant state --that now your switching everyone to this TH2 immune
suppression-- then everyone becomes more susceptible [to infectious
diseases]... and no one is talking about that. Now, a lot of scientists know
that, but they are afraid to speak out because their careers would be
ruined."
Dr. Russell Blaylock M.D.
Neurosurgeon
The Th1/Th2 balance in
autoimmunity.
Th1 and Th2 lymphocytes in
autoimmune disease.
Another explanation:
"Bypassing the mucosal
aspect of the immune system by directly injecting organisms into the body leads
to a corruption in the immune system itself where IgA (Immunoglobulin A) is
transmitted into IgE (Immunoglobulin E), and/or the B cells are hyperactivated
to produce pathological amounts of self-tracking 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
them into ‘L forms,’ leading to a lack of some critical antigens normally
recognized by the cellular immune system.
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 secret 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 can develop leaky gut
syndrome. Crohn’s disease and colitis are also caused by auto-antibody attack
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 unable 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). And on and on and on.
The brain and spinal chord can
also be attacked with auto-antibodies (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,
Guillain-Barré, and seizure disorders."
— Rebecca Carley, MD
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