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Can the immune responses generated by the vaccines create a pattern of immune imbalance that actually compromises the child’s immune system?
We saw how a vaccine-generated Th2 response can burden the body and exhaust the immune system by forcing the body to deal with a chronic ongoing infection. A Th2 response to a specific virus infection will specifically suppress Th1 cells from becoming activated against the same virus. With the resulting failure to generate a Th1 response, cells infected with virus cannot be destroyed. Chronically infected cells, like nerve cells, can occasionally trick the immune system into reacting to and attacking similar nerve cells resulting in autoimmune disease such as multiple sclerosis, Guillain Barré, etc. Cells chronically infected with live vaccine viruses also risk having the viruses mutate, trade genes with each other, as well as interact with the host cell DNA.5 The live vaccines used presently include, measles, mumps, rubella, varicella (chickenpox), and flu-mist. Overactive Th2 activity, underactive Th1 capability, chronic infection, potential for novel virus infection and autoimmunity characterize failed immunostasis or Th-cell imbalance in vaccinated children.
The classic work by Ader & Cohen,6 taught us that the immune system can be classically conditioned. Like Pavlov training dogs to salivate at only a ringing bell, the immune system can be conditioned into inappropriate responses through repeated vaccinations. Natural exposure to the environment and infectious diseases conditions immune responses to be more Th1 dominant; whereas repeated vaccine exposure conditions responses to be more Th2 dominant. A child with Th2-dominance is more susceptible to intracellular organisms such as viruses and is therefore more prone to chronic ear, respiratory, and gastrointestinal infections. Children need a vibrant Th1 response to appropriately deal with the childhood intracellular viral infections, whooping cough, and hemophilus. Healthy immune systems are said to be in Th1/Th2 balance or “immunostasis.” Unhealthy immune systems are said to have a failure in or an imbalance in “immunostasis.” Parris Kidd,7 has compiled a fascinating review indicating that there may be a link between Th1/Th2 balance and disease. Diseases such as allergies, asthma, atopic dermatitis, systemic lupus erythematosus, cancer, tuberculosis, and AIDS, appear to result from a Th2-dominant immune response. It is imperative that we discern the impact of conditioning children’s immune responses to be more Th2 dominant and the consequences of this pattern on the incidence of the Th2-dominant diseases listed by Parris Kidd. When we become Th2 dominant, the antibody-producing part of our immune systems gets derailed like a freight train going a hundred miles per hour, out of control. E. Hurwitz et al has shown that unvaccinated children have less incidence of respiratory conditions, such as asthma and allergies, when compared to their vaccinated counterparts,8 thereby supporting Kidd’s hypothesis.
The focus of much current research is the role of inflammatory responses of varying degrees of severity serving as precursors to cancer, cardiovascular disease, and chronic degenerative diseases being influenced by the different Th cells. Th2 immune responses direct and support bad, excessive inflammation whereas Th1 cells promote healthier type inflammation.
With evidence to support the adverse effects on the immune system by the vaccines, then why do we continue to vaccinate? The role of public health office is to reduce the incidence of infectious disease in the pediatric population. Vaccines generate protective immune responses on a temporary basis and reduce the incidence of infectious disease in the vaccinated kids as well as the unvaccinated kids. Why are the unvaccinated kids protected too? The risk of exposure to the disease is lessened when more individuals are vaccinated. As described, that happens because vaccinated children have tons of antibodies which neutralize infectious virus thereby lessening their ability to spread viruses to others. The phenomenon of unvaccinated children being protected by the vaccinated is known as herd immunity. Herd immunity is a welcomed effect of the vaccination process from a public health perspective. But, according to physicians like James Taylor,9 this may not be a good thing. Unvaccinated children progress into their adult years with a diminished chance of exposure to childhood diseases.
With the passage of time and the vaccinated population not getting their boosters, all become susceptible to the disease. Susceptibility to childhood diseases when we are adults greatly increases severe morbidity and mortality from those diseases. Parents and the powers that-be desire this vaccination approach in order to defer infectious disease to a later date so they do not have to stay home, miss work, and care for a sick child. Th2 dominance from vaccinations results in children being at risk of diseases arising from chronic ongoing infections as well as being vulnerable to the damaging effects of the infectious disease they were vaccinated against when they age and forget about getting booster vaccinations. On the other hand, there are parents anxious to expose their children to the childhood diseases through measles and chickenpox parties so a natural (Th1) immunity can be established early, provide lifelong immunity and appropriately condition the immune system to the natural environment.