What is the Simian 40 (SV40) virus?
This is the re-write of the post that went POOF yesterday lol. Thank you everyone for the amazing info you all shared…….I learn from all of you! I am breaking the SV40 down into 2-3 posts because there is a lot to learn about it!
We will start here:
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC153983/
The simian virus SV40 is a monkey polyomavirus. It is a ZOONOTIC virus, and this study was looking at when/how the virus could enter into a human body. What makes this very scary is that SV40 is highly oncogenic in experimental animals and readily transforms rodent cells in lab cultures. Hamsters inoculated with SV40 develop lymphomas, brain tumors, osteosarcomas, and mesotheliomas. When SV40 infects its natural host, it initially undergoes a lytic replication cycle. The early viral genes encode the tumor (T) antigens: large T antigen (LT), small t antigen (ST), and 17K T antigen. The large T antigen or the LT plays a dominant role in infection, repressing early viral gene transcription and stimulating late viral gene transcription; it is also an initiation factor for viral DNA replication, recruiting the DNA polymerase α-primase complex to the origin of replication. Following the strategy of other DNA viruses, the SV40 early proteins dysregulate the cell cycle and impede cell apoptosis in order to maximize virus production. What does this mean? The virus encodes for tumor creating antigens. It directly inhibits cell death or apoptosis to prevent the tumor encoded cells from dying. They continue to replicate and in the case of a cancerous tumor, they replicate quickly.
How did the SV40 enter into humans? Through the polio virus vaccine. “Melnick and Stinebaugh found SV40 (by cytopathic effects in monkey cells) in the stools of children 3 to 4 weeks after ingestion of SV40 with oral poliovirus vaccine. Morris et al. gave SV40 intranasally to volunteers and found subclinical infections. They were able to isolate virus 7 to 11 days after administration from 3 of 8 subjects, and they detected antibody responses of various amplitudes. Horváth and Fornosi found SV40 excreted in the stools of 10 of 35 children 1 to 2 weeks after being given contaminated oral poliovirus vaccines. Thus, SV40 may replicate in humans after oral administration, but the efficiency and duration of the replication could be dependent on the dose given. The polio vaccine was the introductory vector into humans. The FDA “alleges” that the SV40 gene version of the polio vaccine has not been used since the 1960’s. Do you trust them?
SV40 is likely oncogenic in rodents because the large T antigen (LT) is unable to interact functionally with the rodent DNA polymerase α-primase complex. In this setting, the oncogenic functions of the T antigens are engaged but the productive cycle is not completed, resulting in uncontrolled cell division rather than cell death.
Then we have this paper:
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC452549/
Where did the SV40 come from? Inactivated polio vaccines by Salk and early live attenuated versions from Sabin forms of polio were INADVERTENTLY (uh huh) contaminated with SV40. In addition, different adenovirus vaccines distributed to some U.S. military personnel from 1961 to 1965 also contained SV40. The viral contamination occurred because these early vaccines were prepared in primary cultures of kidney cells derived from rhesus monkeys, which are often naturally infected with SV40. Infectious SV40 survived the vaccine inactivation treatments, and conservative estimates indicate that up to 30 million people (children and adults) in the United States may have been exposed to live SV40 from 1955 through 1963 when administered potentially contaminated polio vaccines. Millions of people worldwide were also potentially exposed to SV40 because contaminated polio vaccines were distributed and used in many countries. These data led the Institute of Medicine to conclude that “the biological evidence is of moderate strength that SV40 exposure from the polio vaccine is related to SV40 infection in humans”
“Persuasive evidence now indicates that SV40 is causing infections in humans today and represents an emerging pathogen. A meta-analysis of molecular, pathological, and clinical data from 1,793 cancer patients indicates that there is a significant excess risk of SV40 associated with human primary brain cancers, primary bone cancers, malignant mesothelioma, and non-Hodgkin's lymphoma. Experimental data strongly suggest that SV40 may be functionally important in the development of some of those human malignancies. Therefore, the major types of tumors induced by SV40 in laboratory animals are the same as those human malignancies found to contain SV40 markers. The Institute of Medicine recently concluded that “the biological evidence is of moderate strength that SV40 exposure could lead to cancer in humans under natural conditions.” This review analyzes the accumulating data that indicate that SV40 is a pathogen which has a possible etiologic role in human malignancies.” This paper was written in 2004. If the polio vaccines were widely used in the 1950-1960’s, then this would be your 40-50 year old age group and up that were developing cancers that were possibly attributed to SV40.
Tomorrow, we will discuss why SV40 is important to understand in current times. Did the SV40 really leave the vaccine industry in the 1960’s? Or has it made a reappearance?
Thanks Jennifer. I recall reading Dr. Judy Mikovits books - she talked about the contamination of the polio "vaccines" - which, when you dig deeper, did absolutely nothing to rid the world of polio. It is very clear that modern "medicine" has created all of today's illness and cancer. On another note, Kevin McKernan ( true genetics expert ) has sequenced Moderna and Pfizer vials and found DNA plasmid contamination. I am not a twitter user but you can browse his posts: https://twitter.com/Kevin_McKernan
Thanks for always telling the truth!
May there be peace on earth. :-)
My dad was born in 1925 and died in 1993 at the age of 67 from a brain tumor, and I've always wondered if SV40 could have been responsible. I think the "40-50 year old age group" as of 2004 is probably too restrictive, and so I asked my buddy chatGPT about the uptake of the vaccines by age group in the 50s and 60s. Here's what it said:
"The Salk polio vaccine was first licensed in 1955 and was initially recommended for use in children aged 6 to 9 years old. Over time, the age range was expanded to include all children up to age 18.
The Sabin oral polio vaccine was licensed in 1962 and was recommended for use in children and adults.
Adults above a certain age were not excluded from receiving the vaccine, but it was primarily targeted at children as they were most at risk for developing paralytic polio.
According to the Centers for Disease Control and Prevention (CDC), by 1963, an estimated 80% of Americans under the age of 40 had received at least one dose of polio vaccine. The percentage of Americans who received the vaccine varied by year, but increased steadily over time. By 1961, over half of all Americans had received the vaccine, and by 1963, over 80% of those under 40 had been vaccinated.
It's worth noting that the polio vaccine was not mandatory, but it was widely recommended by health officials and was considered to be an important public health measure."
I was born in 1952 and distinctly remember as a child drinking the polio vaccine from one of those tiny white paper cups. I even remember thinking "wow, that was easy" as it didn't require a needle!