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The Water Cooler
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CDC admits death toll is inflated! Of 161,392 deaths ONLY 6% / 9,683 ARE DIRECTLY CAUSED BY COVID.
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<blockquote data-quote="_CY_" data-source="post: 3543197" data-attributes="member: 7629"><p>The study Zaks cites at the 3:12 minute mark can be found and read <a href="https://archive.is/o/AI1er/https://www.researchgate.net/publication/316527213_Preclinical_and_Clinical_Demonstration_of_Immunogenicity_by_mRNA_Vaccines_against_H10N8_and_H7N9_Influenza_Viruses" target="_blank">here</a>. The abstract is contained on the <a href="https://archive.is/o/AI1er/https://pubmed.ncbi.nlm.nih.gov/28457665/" target="_blank">NIH Pub Med Library website</a>. In the full test of the study on ResearchGate, the mention of “Luciferase” occurs on page 10. A crucial piece of information in this study is contained on page 4 – “Ferrets immunized with 200 micrograms and challenged [exposed to influenza H7N9 via IN (intranasal)] on day 49 had viral loads below the level of detection”. If a viral load was “below the level of detection”, two questions emerge: 1) did the ferrets even contract H7N9 through intranasal challenge; and, 2) if a viral load is below the level of detection, how do you know the animals even had a viral load? This would bring into question the efficacy of the injection.</p><p>Moreover, the studies Zaks cites as occurring in humans only lasted approximately 18 months.</p><p>At about the 4:00 minute mark, Zaks begins discussing mRNA vaccines for cancer. Immediately following that, Zaks discusses a children’s condition where a gene or “code” is missing that causes production of a certain enzyme critical for metabolism where the current treatment is to transplant an entire organ – in this case, the liver. Zaks proposes to inject mRNA that codes for the missing gene, a gene contained in DNA on the human genome, it would “correct” the genetic defect.</p><p>Ask this question: what causes the cells/body to produce needed enzymes/proteins? Zaks answers that by saying the genetic code or DNA. So, mRNA has to alter a genetic code or the DNA for the body to produce the proteins of COVID-19 for the body to mount an immune response.</p><p></p><p><span style="font-size: 22px"><strong>Preclinical and Clinical Demonstration of Immunogenicity by mRNA Vaccines against H10N8 and H7N9 Influenza Viruses</strong></span></p><p><span style="font-size: 22px"><strong><a href="https://archive.is/GvUjj#selection-1649.33-1649.147" target="_blank">https://archive.is/GvUjj#selection-1649.33-1649.147</a></strong></span></p><p><span style="font-size: 22px"></span></p><p><span style="font-size: 22px"><a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5475249/pdf/main.pdf" target="_blank">https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5475249/pdf/main.pdf</a></span></p><p><span style="font-size: 22px"></span></p><p><span style="font-size: 22px"><span style="font-size: 18px"><strong>Abstract</strong></span></span></p><p><span style="font-size: 22px">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.</span></p><p><span style="font-size: 22px"></span></p></blockquote><p></p>
[QUOTE="_CY_, post: 3543197, member: 7629"] The study Zaks cites at the 3:12 minute mark can be found and read [URL='https://archive.is/o/AI1er/https://www.researchgate.net/publication/316527213_Preclinical_and_Clinical_Demonstration_of_Immunogenicity_by_mRNA_Vaccines_against_H10N8_and_H7N9_Influenza_Viruses']here[/URL]. The abstract is contained on the [URL='https://archive.is/o/AI1er/https://pubmed.ncbi.nlm.nih.gov/28457665/']NIH Pub Med Library website[/URL]. In the full test of the study on ResearchGate, the mention of “Luciferase” occurs on page 10. A crucial piece of information in this study is contained on page 4 – “Ferrets immunized with 200 micrograms and challenged [exposed to influenza H7N9 via IN (intranasal)] on day 49 had viral loads below the level of detection”. If a viral load was “below the level of detection”, two questions emerge: 1) did the ferrets even contract H7N9 through intranasal challenge; and, 2) if a viral load is below the level of detection, how do you know the animals even had a viral load? This would bring into question the efficacy of the injection. Moreover, the studies Zaks cites as occurring in humans only lasted approximately 18 months. At about the 4:00 minute mark, Zaks begins discussing mRNA vaccines for cancer. Immediately following that, Zaks discusses a children’s condition where a gene or “code” is missing that causes production of a certain enzyme critical for metabolism where the current treatment is to transplant an entire organ – in this case, the liver. Zaks proposes to inject mRNA that codes for the missing gene, a gene contained in DNA on the human genome, it would “correct” the genetic defect. Ask this question: what causes the cells/body to produce needed enzymes/proteins? Zaks answers that by saying the genetic code or DNA. So, mRNA has to alter a genetic code or the DNA for the body to produce the proteins of COVID-19 for the body to mount an immune response. [SIZE=6][B]Preclinical and Clinical Demonstration of Immunogenicity by mRNA Vaccines against H10N8 and H7N9 Influenza Viruses[/B] [B][URL]https://archive.is/GvUjj#selection-1649.33-1649.147[/URL][/B] [URL]https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5475249/pdf/main.pdf[/URL] [SIZE=5][B]Abstract[/B][/SIZE][/SIZE] [SIZE=6]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. [/SIZE] [/QUOTE]
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