In the paper by ALDEN M et al, [ Current Issues in Molecular Biology 2022], where the reverse transcription of BNT162b2 into DNA was demonstrated, it is most unfortunate that they didn't use a simple technique to distinguish if the DNA was cDNA or genomic DNA (integrated). In our 2007 paper [Laderoute M et al, AIDS, 2007] we described how uracil N-glycosylase an enzyme that Applied Biosystems Inc uses in some of its buffers to prevent PCR cross contamination which digests cDNA but NOT genomic DNA, we were able to show that an HIV-1 exposed seronegative cohort had about a 5 fold elevated integration (Laderoute M et al., Open AIDS J, 2015) but not detected in patients with HIV. No fancy gene mapping of integration sites needed. However, in their supplementary materials they suggested the largest insert was 30 nt into chromosome 12.
In Dr. McCullough's Substack today there is another of your HERV genes, HERV-W, which contributes to the pathogenesis of the Spike protein and Covid.
I inadvertently listened to "Cross-Country Checkup" yesterday, which was a "Full Court Press" promotion of the (fairly useless) flu shots, and a vigorous endorsement of the Covid shots. We are pushing a boulder up a mountain.
HERV-W is not the same class of retroviruses as the HERV-K HML-2 which defend the human genome against retroviral insertions. Yes, it could contribute to pathogenesis.
i thought one of the main problems with the "vaccines" is that they only stimulate the adaptive immune system (not the innate immune system) to produce antibodies.
In most cases in a naive individual the first dose sets off "trained (innate) immunity" whereas the second dose generates the IgG antibodies to spike {Walsh EE et al., NEJM 2020; Chu l et al., Vaccine May 2021].
If you look at non-COVID deaths, you will see the benefits of trained immunity reduce non-COVID-19 deaths after one dose and no additional benefit with 2 doses [Xu S et al, Dec 14, 2021 MMWR, doi: http://dx.doi.org/10.15585/mmwr.mm7043e2].
In the paper by ALDEN M et al, [ Current Issues in Molecular Biology 2022], where the reverse transcription of BNT162b2 into DNA was demonstrated, it is most unfortunate that they didn't use a simple technique to distinguish if the DNA was cDNA or genomic DNA (integrated). In our 2007 paper [Laderoute M et al, AIDS, 2007] we described how uracil N-glycosylase an enzyme that Applied Biosystems Inc uses in some of its buffers to prevent PCR cross contamination which digests cDNA but NOT genomic DNA, we were able to show that an HIV-1 exposed seronegative cohort had about a 5 fold elevated integration (Laderoute M et al., Open AIDS J, 2015) but not detected in patients with HIV. No fancy gene mapping of integration sites needed. However, in their supplementary materials they suggested the largest insert was 30 nt into chromosome 12.
In Dr. McCullough's Substack today there is another of your HERV genes, HERV-W, which contributes to the pathogenesis of the Spike protein and Covid.
I inadvertently listened to "Cross-Country Checkup" yesterday, which was a "Full Court Press" promotion of the (fairly useless) flu shots, and a vigorous endorsement of the Covid shots. We are pushing a boulder up a mountain.
HERV-W is not the same class of retroviruses as the HERV-K HML-2 which defend the human genome against retroviral insertions. Yes, it could contribute to pathogenesis.
i thought one of the main problems with the "vaccines" is that they only stimulate the adaptive immune system (not the innate immune system) to produce antibodies.
In most cases in a naive individual the first dose sets off "trained (innate) immunity" whereas the second dose generates the IgG antibodies to spike {Walsh EE et al., NEJM 2020; Chu l et al., Vaccine May 2021].
If you look at non-COVID deaths, you will see the benefits of trained immunity reduce non-COVID-19 deaths after one dose and no additional benefit with 2 doses [Xu S et al, Dec 14, 2021 MMWR, doi: http://dx.doi.org/10.15585/mmwr.mm7043e2].