Wednesday, 21 June 2023

 

Monkey Virus DNA Found in COVID-19 Shots

Monkey Virus DNA Found in COVID-19 Shots

The COVID-19 shots are turning out to be more of a time bomb than ever imagined. This new discovery of the presence of monkey virus DNA, including tumor-linked viral promoters, in the jabs has this microbiologist and immunologist calling for an immediate halt in the use of mRNA “vaccines.”

STORY AT-A-GLANCE

  • Microbiologist Kevin McKernan—a former researcher and team leader for the MIT Human Genome Project—has discovered massive DNA contamination in the mRNA COVID-19 shots, including simian virus 40 (SV40) promoters.
  • SV40 has been linked to cancer in humans, including mesotheliomas, lymphomas, and cancers of the brain and bone. In 2002, the Lancet published evidence linking polio vaccines contaminated with SV40 to Non-Hodgkin’s lymphoma. According to the authors, the vaccine may be responsible for up to 50 percent of the 55,000 Non-Hodgkin’s lymphoma cases diagnosed each year.
  • The level of contamination varies depending on the platform used to measure it, but no matter which method is used, the level of DNA contamination is significantly higher than the regulatory limits in both Europe and the United States. The highest level of DNA contamination found was 30 percent.
  • The finding of DNA means the mRNA COVID-19 shots may have the ability to alter the human genome.
  • Even if genetic modification does not occur, the fact that you’re getting foreign DNA into your cells poses a risk in and of itself. Partial expression could occur, or it might interfere with other transcription translations that are already in the cell. Cytoplasmic transfection can also allow for genetic manipulation, as the nucleus disassembles and exchanges cellular components with the cytosol during cell division.

In the video1 above, Dr. Steven E. Greer interviews microbiologist Kevin McKernan—a former researcher and team leader for the MIT Human Genome project2—and Dr. Sucharit Bhakdi about the DNA contamination McKernan’s team has found in the Pfizer and Moderna mRNA shots.

As it turns out, spike protein and the mRNA are not the only hazards of these injections. McKernan’s team has also discovered simian virus 40 (SV40) promoters that, for decades, have been suspected of causing cancer in humans, including mesotheliomas, lymphomas, and cancers of the brain and bone.3 The findings4,5,6,7 were posted on OSF Preprints in early April 2023. As explained in the abstract:8

“Several methods were deployed to assess the nucleic acid composition of four expired vials of the Moderna and Pfizer bivalent mRNA vaccines. Two vials from each vendor were evaluated … Multiple assays support DNA contamination that exceeds the European Medicines Agency (EMA) 330ng/mg requirement and the FDA’s [U.S. Food and Drug Administration]s 10ng/dose requirements …”

As noted by Greer,9 this means that governments and drug companies “have misled the world to a far greater extent than previously known.” If these findings are correct, it would also mean that “the so-called ‘vaccines’ are actually altering the human genome and causing permanent production of the deadly spike protein,” and this internal production of spike protein would, in turn, “trigger the immune system to attack its own cells,” Greer says.

In the interview, McKernan explains how the DNA contaminants found in the COVID-19 jabs can result in the genetic modification of the human genome, and Bhakdi reviews how and why the shots can trigger autoimmune diseases.

Background: What Is SV40?

In 2002, the Lancet published10 evidence linking polio vaccines contaminated with SV40 to Non-Hodgkin’s lymphoma. According to the authors, the vaccine may be responsible for up to half the 55,000 Non-Hodgkin’s lymphoma cases diagnosed each year.

How did this simian (monkey) virus get into the human population? According to the late Dr. Maurice Hilleman, a leading vaccine developer, Merck inadvertently unleashed the virus via their polio vaccine.11 It’s unclear exactly when SV40 was eliminated from the polio vaccine. The timing also varies from country to country. For example, SV40-contaminated polio vaccines were administered in Italy as recently as 1999.12

As reported in a Lancet book review of “The Virus and the Vaccine: The True Story of a Cancer-Causing Monkey Virus, Contaminated Polio Vaccine and the Millions of Americans Exposed”:13

“By 1960, scientists and vaccine manufacturers knew that monkey kidneys were sewers of simian viruses. Such contamination often spoiled cultures, including those of an NIH researcher named Bernice Eddy, who worked on vaccine safety … Her discovery … threatened one of the USA’s most important public-health programs …

“Eddy tried to get word out to colleagues but was muzzled and stripped of her vaccine regulatory duties and her laboratory … [Two] Merck researchers, Ben Sweet and Maurice Hilleman, soon identified the rhesus virus later named SV40—the carcinogenic agent that had eluded Eddy.

“In 1963, U.S. authorities decided to switch to African green monkeys, which are not natural hosts of SV40, to produce polio vaccine. In the mid-1970s, after limited epidemiological studies, authorities concluded that although SV40 caused cancer in hamsters, it didn’t seem to do so in people.

“Fast forward to the 1990s: Michele Carbone, then at NIH [National Institutes of Health], was working on how SV40 induces cancers in animals. One of these was mesothelioma, a rare cancer of the pleura thought in people to be caused mainly by asbestos. The orthodoxy held that SV40 didn’t cause human cancers.

“Emboldened by a 1992 NEJM [New England Journal of Medicine] paper that found DNA ‘footprints’ of SV40 in childhood brain tumors, Carbone tested human mesothelioma tumor biopsies at the National Cancer Institute: 60% contained SV40 DNA. In most, the monkey virus was active and producing proteins.

“He published his results in Oncogene in May, 1994, but the NIH declined to publicize them … Carbone … moved to Loyola University. There he discovered how SV40 disables tumor suppressor genes in human mesothelioma, and published his results in Nature Medicine in July, 1997. Studies in Italy, Germany, and the USA also showed associations between SV40 and human cancers.”

mRNA COVID Jabs Contaminated With Double-Stranded DNA

With that background, let’s get back to McKernan’s findings, which in addition to the featured video are also discussed in Daniel Horowitz’s podcast above. In short, his team discovered elevated levels of double-stranded DNA plasmids, including SV40 promoters (DNA sequence that is essential for gene expression) that are known to trigger cancer development when encountering an oncogene (a gene that has the potential to cause cancer).

The level of contamination varies depending on the platform used to measure it, but no matter which method is used, the level of DNA contamination is significantly higher than the regulatory limits in both Europe and the United States, McKernan says. The highest level of DNA contamination found was 30 percent, which is rather astounding.

As explained by McKernan, when using a typical PCR test, you’ll be considered positive if the test detects the SARS-CoV-2 virus using a cycle threshold (CT) of about 40. In comparison, the DNA contamination is detected at CTs below 20.

That means the contamination is a million-fold greater than the amount of virus you’d need to have in order to test positive for COVID-19. “So, there’s an enormous difference here with regards to the amount of material that’s in there,” McKernan says.

In his Substack article,14 he also points out that people who argue that double-stranded DNA and viral RNA is a false equivalency because viral RNA is replication competent, are wrong.

“The majority of the sgRNA you are detecting in a nasal swab in your nose is NOT REPLICATION COMPETENT as shown in Jaafar et al.15 It is just an RNA fragment that should have lower longevity in your cells than dsDNA contaminating fragments,” he writes.

In that Substack article, McKernan has also copied a 2009 study discussing how DNA in vaccines can cause cancer and highlighted the most relevant parts. It’s a helpful resource if you want to learn more.

Quality Control Is Sorely Lacking

As for how SV40 promoters ended up in the mRNA shots, it appears to be related to poor quality control during the manufacturing process, although it’s unclear where in the development SV40 might have sneaked in. Quality control deficiencies may also be responsible for the high rate of anaphylactic reactions we’ve been seeing. McKernan tells Greer:

“It’s in both Moderna and Pfizer. We looked at the bivalent vaccines for both Moderna and Pfizer and only the monovalent vaccines for Pfizer because we didn’t have access to monovalent vaccines for Moderna. In all three cases, the vaccines contain double-stranded DNA contamination.

“If you sequence that DNA, you’ll find that it matches what looks to be an expression vector that’s used to make the RNA … Whenever we see DNA contamination, like from plasmids, ending up in any injectable, the first thing people think about is whether there’s any E. coli endotoxin present because that creates anaphylaxis for the injected.

“And, of course … there’s a lot of anaphylaxis going on, not only on TV but in the VAERS database. You can see people get injected with this and drop. That could be the background from this E. coli process of manufacturing the DNA …”

Regulatory Agencies Knew There Was a Contamination Problem

In a May 20 Substack article,16 McKernan points out that Pfizer itself submitted evidence to the European Medicines Agency (EMA) showing sampled lots contained vast differences in the levels of double-stranded DNA contamination.

The arbitrary limit for dsDNA that the EMA came up with was 330 nanograms per milligram (ng/mg). Data submitted to the EMA by Pfizer shows sampled lots had anywhere from 1 ng/mg to 815 ng/mg of DNA. McKernan adds:17

“This limit likely did not consider the potency of this dsDNA contamination if it was packaged in an LNP [lipid nanoparticle]. Packaged dsDNA is more potent as a gene therapy. We now know this DNA is packaged and transfection ready.18 Even lower limits should be applied if the DNA is packaged in transfection ready LNPs …

“Even with Pfizer being able to cherry pick the data they provided to the EMA for 10 lots, they see a 1 to 815ng/mg variance. If you were to expand this study to 100 or 1000 lots, you’d likely see another order or two of magnitude variance.”

Double-Stranded DNA May Integrate Into Your Genome

The presence of double-stranded DNA also brings up another major concern, and that is the possibility of genomic integration.

“At least on the Pfizer side of things, it has what’s known as an SV40 promoter. This is an oncogenic virus piece. It’s not the entire virus. However, the small piece is known to drive very aggressive gene expression.

“And the concern that people, even at the FDA, have noted in the past whenever injecting double-stranded DNA, is that these things can integrate into the genome,” McKernan says.

While McKernan’s paper does not present evidence of genome integration, it does point out that it’s possible, especially in the presence of SV40 promoters:19

“There has been a healthy debate about the capacity for SARs-CoV-2 to integrate into the human genome … This work has inspired questions regarding the capacity for the mRNA vaccines to also genome integrate. Such an event would require LINE-1 driven reverse transcription of the mRNA into DNA as described by Alden et al.

“dsDNA [double-stranded DNA] contamination of sequence encoding the spike protein wouldn’t require LINE-1 for Reverse Transcription and the presence of an SV40 nuclear localization signal in Pfizer’s vaccine vector would further increase the odds of integration.”

Manifold Risks

That said, even if genetic modification does not occur, the fact that you’re getting foreign DNA into your cells poses a risk in and of itself, McKernan says. For example, partial expression could occur, or it might interfere with other transcription translations that are already in the cell.

Bhakdi also points out that the SV40 promoters do not need to be present in the nucleus of the cell for problems to occur. Cytoplasmic transfection can, in and of itself, allow for genetic manipulation, because the nucleus disassembles and exchanges cellular components with the cytosol during cell division.

In addition to having DNA floating around and causing potential problems, the RNA in the COVID-19 jab is also modified to resist breakdown. “So, we have TWO versions of the spike protein floating around that can persist longer than anticipated,” McKernan says, and the spike protein, of course, is the most toxic part of the virus that can cause your body to attack itself.

Both McKernan and Bhakdi are adamant that ALL mRNA “vaccines” must be immediately stopped, whether for human or animal use, due to the magnitude of the risks involved.

‘Alarming Problems’

In the video above,20 Yusuke Murakami, a professor at Tokyo University, expresses alarm over the finding of SV40 promoters in the COVID-19 jabs. The interview is in Japanese but has English subtitles. I’ve included it because I think he does a good job of putting the problem into layman’s terms:

“The Pfizer vaccine has a staggering problem,” Murakami says. “This figure is an enlarged view of Pfizer’s vaccine sequence. As you can see, the Pfizer vaccine sequence contains part of the SV40 sequence here. This sequence is known as a promoter.

“Roughly speaking, the promoter causes increased expression of the gene. The problem is that the sequence is present in a well-known carcinogenic virus. The question is why such a sequence that is derived from a cancer virus is present in Pfizer’s vaccine.

“There should be absolutely no need for such a carcinogenic virus sequence in the vaccine. This sequence is totally unnecessary for producing the mRNA vaccine. It is a problem that such a sequence is solidly contained in the vaccine.

“This is not the only problem. If a sequence like this is present in the DNA, the DNA is easily migrated to the nucleus. So it means that the DNA can easily enter the genome. This is such an alarming problem.

“It is essential to remove the sequence. However, Pfizer produced the vaccine without removing the sequence. That is outrageously malicious. This kind of promoter sequence is completely unnecessary for the production of the mRNA vaccine. In fact, SV40 is a promoter of cancer viruses.”

Resources for Those Injured by the COVID Jab

The more we learn about the COVID-19 jabs, the worse they appear. While they suck as vaccines, they’re capable of destroying health in any number of ways, through myriad mechanisms.

If you got one or more jabs and are now reconsidering, first and foremost, never ever take another COVID-19 booster, another mRNA gene therapy shot, or regular vaccine. You need to end the assault on your body. Even if you haven’t experienced any obvious side effects, your health may still be impacted long-term, so don’t take any more shots.

If you’re suffering from side effects, your first order of business is to eliminate the spike protein that your body is producing. Two remedies that can do this are hydroxychloroquine and ivermectin. Both of these drugs bind and facilitate the removal of spike protein.

The Front Line COVID-19 Critical Care Alliance (FLCCC) has developed a post-vaccine treatment protocol called I-RECOVER. Since the protocol is continuously updated as more data become available, your best bet is to download the latest version straight from the FLCCC website at covid19criticalcare.com21 (hyperlink to the correct page provided above).

For additional suggestions, check out the World Health Council’s spike protein detox guide,22 which focuses on natural substances like herbs, supplements, and teas. To combat neurotoxic effects of spike protein, a March 2022 review paper23 suggests using luteolin and quercetin. Time-restricted eating (TRE) and/or sauna therapy can also help eliminate toxic proteins by stimulating autophagy.

Correction: The original headline, ‘Green Monkey DNA Found in COVID-19 Shots,’ has been corrected to ‘Monkey Virus DNA Found in COVID-19 Shots.’ The Epoch Times regrets this error.

Originally published May 31, 2023, on Mercola.com

 References:

Views expressed in this article are the opinions of the author and do not necessarily reflect the views of The Epoch Times. Epoch Health welcomes professional discussion and friendly debate. To submit an opinion piece, please follow these guidelines and submit through our form here.


https://www.theepochtimes.com/health/green-monkey-dna-found-in-covid-19-shots_5317587.html


DNA Virus Monyet Ditemukan dalam Suntikan COVID-19


Tembakan COVID-19 berubah menjadi lebih dari bom waktu daripada yang pernah dibayangkan. Penemuan baru tentang keberadaan DNA virus monyet ini, termasuk promotor virus terkait tumor, dalam suntikan membuat ahli mikrobiologi dan imunologi ini menyerukan penghentian segera dalam penggunaan "vaksin" mRNA.


SEKILAS CERITA


Ahli mikrobiologi Kevin McKernan—mantan peneliti dan pemimpin tim untuk Proyek Genom Manusia MIT—telah menemukan kontaminasi DNA besar-besaran dalam suntikan mRNA COVID-19, termasuk promotor virus simian 40 (SV40).


SV40 telah dikaitkan dengan kanker pada manusia, termasuk mesothelioma, limfoma, dan kanker otak dan tulang. Pada tahun 2002, Lancet menerbitkan bukti yang menghubungkan vaksin polio yang terkontaminasi SV40 dengan limfoma Non-Hodgkin. Menurut penulis, vaksin mungkin bertanggung jawab atas hingga 50 persen dari 55.000 kasus limfoma Non-Hodgkin yang didiagnosis setiap tahun.


Tingkat kontaminasi bervariasi tergantung pada platform yang digunakan untuk mengukurnya, tetapi tidak peduli metode mana yang digunakan, tingkat kontaminasi DNA secara signifikan lebih tinggi daripada batas peraturan di Eropa dan Amerika Serikat. Tingkat kontaminasi DNA tertinggi yang ditemukan adalah 30 persen.


Penemuan DNA berarti suntikan mRNA COVID-19 mungkin memiliki kemampuan untuk mengubah genom manusia.


Bahkan jika modifikasi genetik tidak terjadi, fakta bahwa Anda memasukkan DNA asing ke dalam sel Anda menimbulkan risiko dalam dan dari dirinya sendiri. Ekspresi parsial dapat terjadi, atau mungkin mengganggu terjemahan transkripsi lain yang sudah ada di dalam sel. Transfeksi sitoplasma juga dapat memungkinkan manipulasi genetik, karena inti membongkar dan bertukar komponen seluler dengan sitosol selama pembelahan sel.


Dalam video1 di atas, Dr. Steven E. Greer mewawancarai ahli mikrobiologi Kevin McKernan—mantan peneliti dan pemimpin tim untuk proyek MIT Human Genome2—dan Dr. Sucharit Bhakdi tentang kontaminasi DNA yang ditemukan tim McKernan dalam suntikan mRNA Pfizer dan Moderna.


Ternyata, protein lonjakan dan mRNA bukan satu-satunya bahaya dari suntikan ini. Tim McKernan juga telah menemukan promotor virus simian 40 (SV40) yang, selama beberapa dekade, telah dicurigai menyebabkan kanker pada manusia, termasuk mesothelioma, limfoma, dan kanker otak dan tulang.3 Temuan4,5,6,7 diposting di Preprint OSF pada awal April 2023. Seperti yang dijelaskan dalam abstrak:8


"Beberapa metode digunakan untuk menilai komposisi asam nukleat dari empat botol kedaluwarsa dari vaksin mRNA bivalen Moderna dan Pfizer. Dua botol dari masing-masing vendor dievaluasi ... Beberapa pengujian mendukung kontaminasi DNA yang melebihi persyaratan European Medicines Agency (EMA) 330ng/mg dan FDA [U.S. Administrasi Makanan dan Obat-obatan] persyaratan 10ng/dosis ..."


Sebagaimana dicatat oleh Greer,9 ini berarti bahwa pemerintah dan perusahaan obat "telah menyesatkan dunia ke tingkat yang jauh lebih besar daripada yang diketahui sebelumnya." Jika temuan ini benar, itu juga berarti bahwa "yang disebut 'vaksin' sebenarnya mengubah genom manusia dan menyebabkan produksi permanen protein lonjakan yang mematikan," dan produksi internal protein lonjakan ini akan, pada gilirannya, "memicu sistem kekebalan tubuh untuk menyerang sel-selnya sendiri," kata Greer.


Dalam wawancara, McKernan menjelaskan bagaimana kontaminan DNA yang ditemukan dalam suntikan COVID-19 dapat menghasilkan modifikasi genetik genom manusia, dan Bhakdi meninjau bagaimana dan mengapa suntikan tersebut dapat memicu penyakit autoimun.


Latar Belakang: Apa Itu SV40?


Pada tahun 2002, Lancet menerbitkan 10 bukti yang menghubungkan vaksin polio yang terkontaminasi SV40 dengan limfoma Non-Hodgkin. Menurut penulis, vaksin mungkin bertanggung jawab atas hingga setengah dari 55.000 kasus limfoma Non-Hodgkin yang didiagnosis setiap tahun.


Bagaimana virus simian (monyet) ini masuk ke populasi manusia? Menurut mendiang Dr. Maurice Hilleman, pengembang vaksin terkemuka, Merck secara tidak sengaja melepaskan virus melalui vaksin polio mereka.11 Tidak jelas kapan tepatnya SV40 dieliminasi dari vaksin polio. Waktunya juga bervariasi dari satu negara ke negara lain. Sebagai contoh, vaksin polio yang terkontaminasi SV40 diberikan di Italia baru-baru ini pada 1999.12


Seperti yang dilaporkan dalam ulasan buku Lancet tentang "Virus dan Vaksin: Kisah Nyata Virus Monyet Penyebab Kanker, Vaksin Polio Terkontaminasi, dan Jutaan Orang Amerika Terpapar":13


"Pada tahun 1960, para ilmuwan dan produsen vaksin tahu bahwa ginjal monyet adalah selokan virus simian. Kontaminasi seperti itu sering merusak budaya, termasuk seorang peneliti NIH bernama Bernice Eddy, yang bekerja pada keamanan vaksin ... Penemuannya ... mengancam salah satu program kesehatan masyarakat paling penting di AS ...


"Eddy mencoba menyampaikan kabar kepada rekan kerja tetapi diberangus dan dilucuti dari tugas pengaturan vaksinnya dan laboratoriumnya ... [Dua] peneliti Merck, Ben Sweet dan Maurice Hilleman, segera mengidentifikasi virus rhesus yang kemudian bernama SV40—agen karsinogenik yang telah menghindari Eddy.


"Pada tahun 1963, otoritas AS memutuskan untuk beralih ke monyet hijau Afrika, yang bukan inang alami SV40, untuk memproduksi vaksin polio. Pada pertengahan 1970-an, setelah studi epidemiologi yang terbatas, pihak berwenang menyimpulkan bahwa meskipun SV40 menyebabkan kanker pada hamster, tampaknya tidak melakukannya pada manusia.


“Maju cepat ke tahun 1990-an: Michele Carbone, saat itu di NIH [Institut Kesehatan Nasional], sedang mengerjakan bagaimana SV40 menginduksi kanker pada hewan. Salah satunya adalah mesothelioma, kanker pleura langka yang diperkirakan pada orang terutama disebabkan oleh asbes. Ortodoksi menyatakan bahwa SV40 tidak menyebabkan kanker manusia.


"Dicerakkan oleh makalah NEJM [New England Journal of Medicine] 1992 yang menemukan 'jejak kaki' DNA SV40 pada tumor otak masa kanak-kanak, Carbone menguji biopsi tumor mesothelioma manusia di National Cancer Institute: 60% mengandung DNA SV40. Pada sebagian besar, virus monyet aktif dan memproduksi protein.


“Dia menerbitkan hasilnya di Oncogene pada Mei 1994, tetapi NIH menolak untuk mempublikasikannya ... Carbone ... pindah ke Universitas Loyola. Di sana dia menemukan bagaimana SV40 menonaktifkan gen penekan tumor pada mesothelioma manusia, dan menerbitkan hasilnya di Nature Medicine pada Juli 1997. Studi di Italia, Jerman, dan Amerika Serikat juga menunjukkan hubungan antara SV40 dan kanker manusia.”


Suntan COVID mRNA Terkontaminasi Dengan DNA Untai Ganda


Dengan latar belakang itu, mari kita kembali ke temuan McKernan, yang selain video unggulan juga dibahas dalam podcast Daniel Horowitz di atas. Singkatnya, timnya menemukan peningkatan kadar plasmid DNA untai ganda, termasuk promotor SV40 (urutan DNA yang penting untuk ekspresi gen) yang diketahui memicu perkembangan kanker ketika menghadapi onkogen (gen yang berpotensi menyebabkan kanker).


Tingkat kontaminasi bervariasi tergantung pada platform yang digunakan untuk mengukurnya, tetapi tidak peduli metode mana yang digunakan, tingkat kontaminasi DNA secara signifikan lebih tinggi daripada batas peraturan di Eropa dan Amerika Serikat, kata McKernan. Tingkat kontaminasi DNA tertinggi yang ditemukan adalah 30 persen, yang agak mencengangkan.


Seperti yang dijelaskan oleh McKernan, ketika menggunakan tes PCR tipikal, Anda akan dianggap positif jika tes mendeteksi virus SARS-CoV-2 menggunakan ambang siklus (CT) sekitar 40. Sebagai perbandingan, kontaminasi DNA terdeteksi pada CT di bawah 20.


Itu berarti kontaminasi satu juta kali lipat lebih besar dari jumlah virus yang perlu Anda miliki untuk dites positif COVID-19. "Jadi, ada perbedaan besar di sini sehubungan dengan jumlah materi yang ada di sana," kata McKernan.


Dalam artikel Substack-nya,14 dia juga menunjukkan bahwa orang-orang yang berpendapat bahwa DNA untai ganda dan RNA virus adalah kesetaraan yang salah karena RNA virus adalah replikasi yang kompeten, salah.


"Mayoritas sgRNA yang Anda deteksi dalam usap hidung di hidung Anda BUKAN REPLIKASI KOMPETEN seperti yang ditunjukkan dalam Jaafar et al.15 Ini hanyalah fragmen RNA yang seharusnya memiliki umur panjang yang lebih rendah di sel Anda daripada fragmen yang mencemari dsDNA," tulisnya.


Dalam artikel Substack itu, McKernan juga telah menyalin studi tahun 2009 yang membahas bagaimana DNA dalam vaksin dapat menyebabkan kanker dan menyoroti bagian yang paling relevan. Ini adalah sumber yang bermanfaat jika Anda ingin mempelajari lebih lanjut.


Kontrol Kualitas Sangat Kurang


Adapun bagaimana promotor SV40 berakhir di tembakan mRNA, tampaknya terkait dengan kontrol kualitas yang buruk selama proses manufaktur, meskipun tidak jelas di mana dalam pengembangan SV40 mungkin telah menyelinap masuk. Kekurangan kontrol kualitas mungkin juga bertanggung jawab atas tingginya tingkat reaksi anafilaksis yang telah kita lihat. McKernan memberi tahu Greer:


"Itu ada di Moderna dan Pfizer. Kami melihat vaksin bivalen untuk Moderna dan Pfizer dan hanya vaksin monovalen untuk Pfizer karena kami tidak memiliki akses ke vaksin monovalen untuk Moderna. Dalam ketiga kasus, vaksin mengandung kontaminasi DNA untai ganda.


"Jika Anda mengurutkan DNA itu, Anda akan menemukan bahwa itu cocok dengan apa yang tampak seperti vektor ekspresi yang digunakan untuk membuat RNA ... Setiap kali kita melihat kontaminasi DNA, seperti dari plasmid, berakhir dengan suntikan apa pun, hal pertama yang dipikirkan orang adalah apakah ada endotoksin E. coli karena itu menciptakan anafilaksis untuk yang disuntikkan.


“Dan, tentu saja ... ada banyak anafilaksis yang terjadi, tidak hanya di TV tetapi di database VAERS. Anda dapat melihat orang-orang disuntik dengan ini dan jatuh. Itu bisa menjadi latar belakang dari proses pembuatan DNA E. coli ini ...”


Badan Pengatur Tahu Ada Masalah Kontaminasi


Dalam artikel Substack 20 Mei,16 McKernan menunjukkan bahwa Pfizer sendiri menyerahkan bukti ke European Medicines Agency (EMA) yang menunjukkan lot sampel mengandung perbedaan besar dalam tingkat kontaminasi DNA untai ganda.


Kekhawatiran yang telah dicatat orang-orang, bahkan di FDA, di masa lalu setiap kali menyuntikkan DNA untai ganda, adalah bahwa hal-hal ini dapat berintegrasi ke dalam genom.


— Kevin McKernan


Batas sewenang-wenang untuk dsDNA yang muncul dari EMA adalah 330 nanogram per miligram (…



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