Mary Ferrie and the Monkey Virus

[Steven Gaal]

http://www.conspiracyplanet.com/channel.cfm?channelid=47&contentid=7886 cancer in vaccines BELOW AT BOTTOM Ive placed three PUB MED references that add to this video. Polio vaccine was sent to Russia.

http://www.amazon.com/Mary-Ferrie-Monkey-Virus-Underground/dp/0964398125 lots of bucks. Maybe someone bought them up? If so ,who would that be ? wow I got 2 of these books (one signed). sg

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http://www.amazon.com/Virus-Vaccine-Contaminated-Cancers-Government/dp/0312342721/ref=pd_cp_b_2

Amazon.com Review

Past tragedies caused by "miracle drugs" have taught the public to approach cures with caution, and vaccines, in particular, have come under public scrutiny. In The Virus and the Vaccine, journalists Debbie Bookchin and Jim Schumacher uncover the true tale of the polio vaccine and its past and present dangers. Like many medical detective stories before it, this book starts with a chilling anecdote, then flashes back to slowly set the stage for disaster. Baby boomers who only know Jonas Salk and his virus-fighting colleagues as heroes will be disturbed at how some of them downplayed concerns about a monkey virus called SV40 that was present in the polio vaccine. The links between SV40 and human cancer took a long time to define, and breakthroughs in molecular biology made the job more realistic in later decades. Nevertheless, Bookchin and Schumacher argue that a biased scientific bureaucracy in combination with a desperate public and money-hungry pharmaceutical! companies fostered the use of a vaccine that may have increased cancer risk. "The vast majority of baby boomers--almost all of whom received polio vaccine in the late 1950s and early 1960s--have potentially been exposed to the virus," they write. But baby boomers aren't the only ones at risk. The authors reveal that Lederle Laboratories continued to produce potentially contaminated oral polio vaccines well into the 1990s. Although the authors point fingers of blame at some specific targets, they carefully balance their accusations with reminders that public demands for cures must be balanced with careful assessment of new medical treatments. --Therese Littleton --This text refers to an out of print or unavailable edition of this title.

From Publishers Weekly

Journalists Bookchin and Schumacher argue that for nine years, from 1954 to 1963, almost every dose of polio vaccine produced in the worldâ€"and the 98 million Americans who received polio vaccinationsâ€"was contaminated with a cancer-causing virus from the monkey kidneys used to develop the vaccine. Although the polio vaccine developed by Dr. Jonas Salk virtually ended polio as a threatening disease, the authors detail how "the screening techniques and observation periods that Salk and the vaccine manufacturers employed were not capable of always catching the contaminants." This sordid story spells out how repeated research studies showing that the "SV40" virus was in the vaccine were dismissed by federal health officials, so that "there would be no warning to consumers that the vaccine they and their children were receiving contained a live monkey virus whose effect on humans was entirely unknown." In the second part, the authors contend that even today such organizations as the National Institutes of Health continue to dismiss study results, even though numerous studies have shown that SV40 is capable of causing cancer in humans. The final and most horrific part of the story reports that Lederle Laboratories, the sole oral vaccine supplier in the U.S. from 1977 onward, continued to use monkey kidneys possibly infected by the SV40 virus in its manufacturing process until oral polio vaccine was removed from the market as late as January 2000. This meticulously researched, levelheaded and well-written book should stir up considerable debate. Because the authors never become alarmist, this solid work of investigative reporting carries considerable weight, and deserves to be read by a large audience.

Copyright © Reed Business Information, a division of Reed Elsevier Inc. All rights reserved. --This text refers to an out of print or unavailable edition of this title.

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Bull Exp Biol Med. 2009 Dec;148(6):924-6.

Epidemiology of SV-40 simian virus in different regions of the Russian federation.

Lapin BA, Chikobava MG.

Institute of Medical Primatology, Russian Academy of Medical Sciences, SochiAdler, Russia. blapin@yandex.ru

Abstract

Multiplication of poliomyelitis virus for vaccine production in 1955-1961 was realized in kidney cell culture from M. rhesus naturally infected with SV-40 simian virus. Hence, some lots of the vaccine were contaminated with this virus. It was found that SV-40 is oncogenic for laboratory rodents. Since 1963, in accordance with WHO recommendation, green monkey kidneys containing no SV-40 were used instead of M. rhesus kidneys. Overall vaccination of the population with poliomyelitis vaccine in 1955-1961 led to infection of many humans in Russia and many foreign countries with SV-40. The possibility of horizontal transmission of the virus was demonstrated. As a result, virus (its DNA sequences) was detected in individuals who were never vaccinated. Hundreds of reports, often contradictory, discuss this problem. Our study is based on the analyses of 460 blood specimens from subjects living in different regions of Russia (Krasnodar region, Moscow, Novosibirsk region, Krasnoyarsk territory). The percent of individuals infected with SV-40 varies from 16 to 49%.

PMID: 21116508 [PubMed - in process]

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J Virol. 2009 Apr;83(7):3402-6. Epub 2009 Jan 7.

Evolution of the Sabin vaccine into pathogenic derivatives without appreciable changes in antigenic properties: need for improvement of current poliovirus surveillance.

Yakovenko ML, Korotkova EA, Ivanova OE, Eremeeva TP, Samoilovich E, Uhova I, Gavrilin GV, Agol VI.

M. V. Lomonosov Moscow State University, Moscow 119899, Russia.

Abstract

The Sabin oral polio vaccine (OPV) may evolve into pathogenic viruses, causing sporadic cases and outbreaks of poliomyelitis. Such vaccine-derived polioviruses (VDPV) generally exhibit altered antigenicity. The current paradigm to distinguish VDPV from OPV and wild polioviruses is to characterize primarily those poliovirus isolates that demonstrate deviations from OPV in antigenic and genetic intratypic differentiation (ITD) tests. Here we report on two independent cases of poliomyelitis caused by VDPVs with "Sabin-like" properties in several ITD assays. The results suggest the existence of diverse pathways of OPV evolution and necessitate improvement of poliovirus surveillance, which currently potentially misses this class of VDPV.

PMID: 19129444 [PubMed - indexed for MEDLINE]PMCID: PMC2655595Free PMC Article

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2.Cancer Cell Int. 2010 Feb 23;10:4.

Transformation of SV40-immortalized human uroepithelial cells by 3-methylcholanthrene increases IFN- and Large T Antigen-induced transcripts.

Crosby LM, Moore TM, George M, Yoon LW, Easton MJ, Ni H, Morgan KT, DeAngelo AB.

Environmental Carcinogenesis Division, National Health Effects and Environmental Research Laboratory, US Environmental Protection Agency, Research Triangle Park, USA. lcrosby@uthsc.edu

Abstract

BACKGROUND: Simian Virus 40 (SV40) immortalization followed by treatment of cells with 3-methylcholanthrene (3-MC) has been used to elicit tumors in athymic mice. 3-MC carcinogenesis has been thoroughly studied, however gene-level interactions between 3-MC and SV40 that could have produced the observed tumors have not been explored. The commercially-available human uroepithelial cell lines were either SV40-immortalized (HUC) or SV40-immortalized and then 3-MC-transformed (HUC-TC).

RESULTS: To characterize the SV40 - 3MC interaction, we compared human gene expression in these cell lines using a human cancer array and confirmed selected changes by RT-PCR. Many viral Large T Antigen (Tag) expression-related changes occurred in HUC-TC, and it is concluded that SV40 and 3-MC may act synergistically to transform cells. Changes noted in IFP 9-27, 2'-5' OAS, IF 56, MxA and MxAB were typical of those that occur in response to viral exposure and are part of the innate immune response. Because interferon is crucial to innate immune host defenses and many gene changes were interferon-related, we explored cellular growth responses to exogenous IFN-gamma and found that treatment impeded growth in tumor, but not immortalized HUC on days 4 - 7. Cellular metabolism however, was inhibited in both cell types. We conclude that IFN-gamma metabolic responses were functional in both cell lines, but IFN-gamma anti-proliferative responses functioned only in tumor cells.

CONCLUSIONS: Synergism of SV40 with 3-MC or other environmental carcinogens may be of concern as SV40 is now endemic in 2-5.9% of the U.S. population. In addition, SV40-immortalization is a generally-accepted method used in many research materials, but the possibility of off-target effects in studies carried out using these cells has not been considered. We hope that our work will stimulate further study of this important phenomenon.

PMID: 20178601 [PubMed]PMCID: PMC2848030Free PMC Article

Edited February 20, 2011 by Steven Gaal

[David Andrews]

Again, people who really want to see how investigative journalists ought to research Alton Ochsner and weaponized virology should compare how polio and AIDS are examined in this documentary, The Origin of AIDS:

http://www.imdb.com/title/tt0438938/

Which can be watched here:

http://freedocumentaries.org/film.php?id=123

And is based on this book, The River, by Edward Hooper:

http://www.amazon.com/River-Journey-Source-HIV-AIDS/dp/0316371378/ref=sr_1_1?ie=UTF8&qid=1298211162&sr=8-1

Edited February 20, 2011 by David Andrews