TH1 & TH2
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.
https://www.ncbi.nlm.nih.gov/m/pubmed/8679122/
Th1 and Th2 lymphocytes in autoimmune disease.
https://www.ncbi.nlm.nih.gov/m/pubmed/15952931/
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