Millions of Children Infected with 'Vaccine Safety Experts' Rotateq Vaccine: Dr. Paul Offit


BREAKING NEWS: Millions of Children Infected with 'Vaccine Safety Experts' Rotateq Vaccine: Dr. Paul Offit

Paul Offit says you can safely administer 10,000 vaccines to infants at once. But he also profits from the patent he holds for the Rotateq vaccine. What's wrong with this picture? 

Dr. Paul Offit is a pediatrician who co-invented a rotavirus vaccine (trade name Rotateq), who once stated in interview that a child can be administered 100,000 vaccines safely at once (later revised to 10,000). A professor of Pediatrics at the University of Pennsylvania, he is the darling of the mainstream media and a widely cited self-appointed 'vaccine safety expert,' despite the glaring conflict of interest implied by such a designation.

Unfortunately for Dr. Offit (not so affectionately named Dr. Profit), a 2010 study published in Journal of Virology revealed that his multi-million dollar grossing patent on the Rotateq vaccine contains a live simian retrovirus (with a 96% match of certainty) that has likely infected millions of children over the past few years with a virus that causes great harm.  Retrovirus infections are permanent, and can carry on indefinitely into future generations. In other words, once they are inserted into the human genome they can not be removed. View the entire PDF here.

Moreover, a 2014  study published in Advances in Virology found Dr. Offit's vaccine contains a "a baboon endogenous virus strain M7...likely due to the monkey cell line in which RotaTeq was produced from." View the entire PDF here.

In order to grasp the dire significance of these findings, you might want to familiarize yourself with the history of adventitious viruses in so-called attenuated or live vaccines. These contain the actual disease vector they are supposed to prevent. While considered "weakened," their process of manufacture often make them more adaptable to the host within which they are injected. Many rounds of passage through human and animal cells often makes these vaccines far more dangerous than the natural 'wild-type' infections that we encounter naturally. You only have to look to oral polio vaccine to understand the dangers of the vaccine model. In 2011, the Indian Journal of Medical Ethics published a study revealing that vaccine strain polio is twice as lethal as wild-type, and has been identified to cause over 47,000 cases of polio-associated paralysis in 2011 alone. This was the vaccine launched by the Dali Lama himself, who apparently has no clue as to the harm caused by these interventions.

The theory is that by infecting healthy bodies with them you generate an immune response – validated by elevated antibody titers, regardless of their affinity to the pathogen – that results (in theory) in increased protection.  Regardless of the justification for using monkey cells for vaccine production, monkey retroviruses contaminate the vaccines nonetheless. By unintentionally infecting healthy infants with these viruses you are making them sick. Retroviruses use reverse transcriptase – a viral enzyme – to insert pathogenic genetic information into healthy cells, effectively converting them into virus-manufacturing factories. And no matter what your medical philosophy is, monkey viruses have no justifiable place in a healthy human body.

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Your article about Rototec vaccine and Dr. Paul Offit



In a thorough reading of the two PDF studies provide within your article, I can find nothing to support what you claim in your article.  What gives?  I shared your article on my FB page and a friend with extensive education in science/chemistry jumped all over it. Then I went back and read carefully those two pdf sources and had to agree with her. Are there other sources you neglected to share?

 

RE: Rotateq



This should help, from one of our advisers Judy Mikovits, PhD:

"It is simply misrepresentation of the literature and available data to suggest the presence of these retroviruses elements are of no concern simply because they are not replication competent.  There is a body of literature of more than two decades showing defective retroviral elements can have deleterious effects in humans.

There are four primary areas of concern; these elements can:

1) alter DNA methylation machinery

2) stimulate proinflammatory cytokiness and chemokines and thus the expression of latent retroviruses (both exogenous and endogenous)

3) alter cellular gene function through insertional mutagenesis or altered expression of microRNA or other regulatory elements3)

4) recombine with human endogenous elements whose expression and methylation is also altered by the expression and integration and presence of defective retroviruses

Since the sequencing of the human genome in 2003, numerous SNPs have been identified in key molecular pathways in response to viral elements.The genetically susceptible populations such as those with the inability to degrade these elements (RNASEL) defects APOBEC editing or methylation machinery (MTHFR) are hypothesized to be among the vaccine injured.  You also discussed the Thompson paper. It is our hypothesis that defects in the RNASEL pathway may in part be an explantation for the increased risk of autism in back males following MMR vaccinations. Had those data not been censored or cherry picked we (the scientific community) could have prevented much suffering. Special interests and politics have no role in scientific discovery and the protection of public health.

References

Mikovits, J. A., Young, H. A., Vertino, P., Issa, J. P. J., Pitha, P. M., Turcoski-Corrales, S., Taub, D. D., Petrow, C. L., Baylin, S. B., and Ruscetti, F. W.: HIV-1 infection upregulates DNA methyltransferase resulting in de novo methylation of the IFN-gamma promoter and subsequent downregulation of IFN-gamma production. Mol. Cell. Biol.,18:5166-5177, 1998. 

J. Mikovits , F. Ruscetti, W. Zhu, R. Bagni, D. Dorjsuren and R. Shoemaker. Potential Cellular Signatures of Viral Infections in Human Hematopoietic Cells. Disease Markers. 2001;17(3):173-8.

 J-Y Fang, JA Mikovits, R Bagni, CL Petrow-Sadowski and FW Ruscetti. Infection of Lymphoid Cells by Integration-Defective HIV-1 increases De Novo Methylation. J Virol. 2001. 75: 9753-9761. 

Mikovits, J. A., Lohrey, N. C., Schuloff, R., Courtless, J. and Ruscetti, F. W.: Immune activation of HIV expression from latently infected monocytes from asymptomatic seropositive patients. J. Clin. Invest. 90: 1486-1491, 1992.

Muegge K, Young H, Ruscetti F, Mikovits J Epigenetic control during lymphoid development and immune responses: aberrant regulation, viruses, and cancer. Ann N Y Acad Sci. 2003 Mar; 983:55-70. Review

 Zhang et al.,  Cancer, Biol. Ther.  2011, 12:617

Laderoute M et al. The replicative ability of Human Endogenous retrovirus K 102 with HIV viremia. AIDS. 2007, 21:2417-2424

 Delviks-Frankenbery K et al. Generation of Multiple Replication-Competent Retroviruses through Recombination between PreXMRV-1 and PreXMRV-2 2013 J.Virol

 Murgai M., et. al. Xenotropic MLV Env proteins induce tumor cells to secrete factors that promote the formation of immature blood vessels. Retrovirology 2013 10:34

 

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