Immune Dysregulation in Autism Spectrum Disorder: What Do We Know about It?
Over 200 Peer-Reviewed Papers on Immune System Related to Common Childhood Problem
By Peter A. McCullough, MD, MPH
The race is on to find determinants or risk factors for autism that could be modified or eliminated in order to stem the tide of new cases. One of the hottest areas of research is immune dysregulation causing changes during the development of the human brain that result in the expression of autism spectrum disorder.
de los Angeles Robinson-Agramonte published an exhaustive review on the topic with 236 references. I did a PUBMED search and also found > 200 papers. The evidence for immune system involvement in autism is overwhelming. The next question in the chain of logic is: “What common immune system perturbation occurs in nearly every child over multiple exposures during childhood?” Obvious exposures must include intensive childhood hyper-vaccination, that is, giving multiple antigens/killed/live-attenuated viruses to small children in the same dose administration which is common practice with the ever-expanding vaccine schedule.
The authors point out that both adjuvants in vaccines (e.g. thiomersal) and antibodies against vaccine induced antigens (e.g. measles) have been associated with autism. The next steps in research are carefully controlled prospective studies of immunological markers in those hyper-vaccinated with periodic assessment for the outcome of autism spectrum disorder. While more parents are opting out of the CDC ACIP childhood vaccine schedule, there are plenty more who should be willing to participate in this important research area.
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Just a simple comment on giving multiple vax in ONE shot:
-- If you wanted to cover up the effects of one ingredient, inject it with lots of other stuff so the there is huge interaction between them.
-- Statistically Designed experiments in industry purposely keep the number of variables to the minimum level so "confounded variation" does not obscure the results and interpretation has more significance.
-- Having 2 or 3 vaccines + adjuvants + no controls is a recipe to make forensics impossible
ANY scientist who has EVER performed a REAL experiment KNOWS by now that the FDA does not have human interest in life at heart.
My grandson(whom I have raised) got the big doses of thimerosal in vaccines as he was born in 1997.
Attemps at chelating and removing the mercury have always failed. During chelation, we have seen mega doses of other toxins come out like aluminum, cadmium, lead and even tin etc etc. The likely inference has always been that babies and toddlers given vaccines with mercury and having a genetic predisposition to not be able eliminate it quickly from the body-that after 2 weeks the mercury will corss the B/B barrier and later enter all the organs of the body where removing it has been virtually impossible. The genetic predisposition I've always read about has been low glutathione levels and thus having an effect on a good methylation system(plus the MTHFR gene)plus being born with high levels of testosterone. He was diagnosed with autism at age 2, but showed earlier signs of it prior to age 2. He's now 25 and although he is ever so much better, I have yet been unable to completely recover him. Verbal repetition has become his biggest stumbling block. (PANS, PANDAS. I know they are now doing clinical trials with suramin(Bradstreet's challenge before he died) I am still unable to get a hold of it to try). May God bless the millions with autism that our government, Pharma and most doctors have ignored for 25 years.