Macaque Experiment Fails To Link Vaccine Schedule And Autism

pete

Member
Joined
Aug 31, 2012
Messages
139
http://www.cdc.gov/vaccines/pubs/pinkbook/downloads/appendices/B/excipient-table-2.pdf

MMR (MMR-II)

Medium 199 (vitamins, amino acids, fetal bovine serum, sucrose,
glutamate) , Minimum Essential Medium, phosphate, recombinant human
albumin, neomycin, sorbitol, hydrolyzed gelatin, chick embryo cell
culture, WI-38 human diploid lung fibroblasts

MMRV (ProQuad)

sucrose, hydrolyzed gelatin, sorbitol, monosodium L-glutamate, sodium
phosphate dibasic, human albumin, sodium bicarbonate, potassium
phosphate monobasic, potassium chloride, potassium phosphate dibasic,
neomycin, bovine calf serum, chick embryo cell culture, WI-38 human
diploid lung fibroblasts, MRC-5 cells
 

pete

Member
Joined
Aug 31, 2012
Messages
139
Impact of environmental factors on the prevalence of autistic disorder after 1979
Theresa A. Deisher*, Ngoc V. Doan, AngelicaOmaiye, Kumiko Koyama and Sarah Bwabye
Journal of Public Health and Epidemiology
Received 13 May, 2014; Accepted 9 July, 2014

The children vaccinated with MMRII, Varicella and Hepatitis A vaccines varied from 19 to 35 months of age at the time of vaccination. [highlight=yellow]Autistic disorder birth year change points were identified as 1980.9, 1988.4 and 1996 for the US[/highlight], 1987 for UK, 1990.4 for Western Australia, and 1987.5 for Denmark.

[highlight=yellow]Change points in these countries corresponded to introduction of or increased doses of human fetal cell line-manufactured vaccines[/highlight], while no relationship was found between paternal age or Diagnostic and Statistical Manual (DSM) revisions and autistic disorder diagnosis.

Further, linear regression revealed that Varicella and Hepatitis A immunization coverage was significantly correlated to autistic disorder cases. R software was used to calculate change points.

[highlight=yellow]Autistic disorder change points years are coincident with introduction of vaccines manufactured using human fetal cell lines, containing fetal and retroviral contaminants[/highlight], into childhood vaccine regimens.

This pattern was repeated in the US, UK, Western Australia and Denmark. [highlight=yellow]Thus, rising autistic disorder prevalence is directly related to vaccines manufactured utilizing human fetal cells[/highlight]. Increased paternal age and DSM revisions were not related to rising autistic disorder prevalence.
 
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