MODERNA: Tal Zaks 2017 TEDx Talk Promoting "GENE EDITING" mRNA Vaccines

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Harold Saive

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Apr 18, 2022, 6:22:03 AM4/18/22
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Moderna TEDx Talk: mRNA Vaccine Technology (PROMOTION VIDEO 2017)
https://youtu.be/AHB2bLILAvM

Moderna TEDx Talk: mRNA Vaccine Technology (PROMOTION VIDEO 2017)
Tal Zaks from Moderna sells you the mRNA Vaccine technology used in the COVID-19 "vaccines" a.k.a experimental gene therapies. He proudly promotes they are "hacking the software of life" and they call it "information therapy". They see the body "as an operating system" to reprogram and he admits TWICE that they don't know if it's going to work. Not one single product ever approved for use because of its dangers and the COVID-19 "vaccines" are for emergency use only. This is a version with improved subtitles, pointing out IN CAPS the most interesting things he says.
https://www.brighteon.com/3f1e4cd4-7fe8-43a2-868a-8732731e2ab6

TEDx Program
https://www.ted.com/about/programs-initiatives/tedx-program

The War on Cancer has been raging for over a century, and Tal Zaks may have the biggest breakthrough yet. His idea, to go straight to the source of the problem and edit the genetic code that causes the body to produce cancerous cells, could save millions of lives without a single surgery or chemotherapy regimen. Tal Zaks is the Chief Medical Officer of Moderna Therapeutics.

Tal Zaks is the Chief Medical Officer of Moderna Therapeutics. This talk was given at a TEDx event using the TED conference format but independently organized by a local community. Learn more at https://www.ted.com/tedx

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Preclinical and Clinical Demonstration of Immunogenicity by mRNA Vaccines against H10N8 and H7N9 Influenza Viruses (2017)
Kapil Bahl,1 Joe J. Senn,2 Olga Yuzhakov,1 Alex Bulychev,2 Luis A. Brito,2 Kimberly J. Hassett,1 Michael E. Laska,2 Mike Smith,2 Örn Almarsson,2 James Thompson,2 Amilcar (Mick) Ribeiro,1 Mike Watson,1 Tal Zaks,2 and Giuseppe Ciaramella1
(Published online 2017 Apr 27)

Recently, the World Health Organization confirmed 120 new human cases of avian H7N9 influenza in China resulting in 37 deaths, highlighting the concern for a potential pandemic and the need for an effective, safe, and high-speed vaccine production platform. Production speed and scale of mRNA-based vaccines make them ideally suited to impede potential pandemic threats. Here we show that lipid nanoparticle (LNP)-formulated, modified mRNA vaccines, encoding hemagglutinin (HA) proteins of H10N8 (A/Jiangxi-Donghu/346/2013) or H7N9 (A/Anhui/1/2013), generated rapid and robust immune responses in mice, ferrets, and nonhuman primates, as measured by hemagglutination inhibition (HAI) and microneutralization (MN) assays. A single dose of H7N9 mRNA protected mice from a lethal challenge and reduced lung viral titers in ferrets. Interim results from a first-in-human, escalating-dose, phase 1 H10N8 study show very high seroconversion rates, demonstrating robust prophylactic immunity in humans. Adverse events (AEs) were mild or moderate with only a few severe and no serious events. These data show that LNP-formulated, modified mRNA vaccines can induce protective immunogenicity with acceptable tolerability profiles.

Keywords: mRNA vaccines, influenza, immunogenicity, pandemic, vaccines, H10N8, H7N9, mRNA
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5475249/

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