sublimesatanist
Active member
I did some reading into this and I want to share what I learned. This is important information because it proves they are making permanent changes to the human genome. This might be a bit tedious to read but it has some riveting information.
SARS-CoV-2 Spike Impares DNA Damage Repair and Inhibits V(D)J Recombination in Vitro:
"Here, by using an in vitro cell line, we report that the SARS-CoV-2 spike protein significantly inhibits DNA damage repair, which is required for effective V(D)J recombination in adaptive immunity. Mechanistically, we found that the spike protein localizes in the nucleus and inhibits DNA damage repair by impeding key DNA repair protein BRCA1 and 53BP1 recruitment to the damage site."
("V(D)J recombination is the mechanism of somatic recombination that occurs only in developing lymphocytes during the early stages of T and B cell maturation. It results in the highly diverse repertoire of antibodies/immunoglobulins and T cell receptors (TCRs) found in B cells and T cells, respectively. The process is a defining feature of the adaptive immune system." - Wikipedia)
It's important to understand these two pathways, Non-homogulous end joining (NHEJ) and Homologous Recombination (HR) as explained in another quote:
"NHEJ repair and holologus recombination repair are two major DNA repair pathways that not only continuously monitor and ensure genome integrity but are also vital for adaptive immune cell functions."
From study "Comparison of nonhomologous end joining and homologous recombination in human cells:"
"...we conclude than in proliferating cells NHEJ repairs 75% of DSBs while HR repairs the remaining 25%."
The scientists (from the first study mentioned) used DNA treatments on damaged cells and tested them for SARS-CoV-2 proteins. The spike protein (in both NHEJ and HR) had an efficiency rate of around 10% and 20%, which means it inhibits this repair mechanism by 80% to 90%. (See slide below).
"To determine how the spike protein inhibits both NHEJ and HR repair pathways, we analyzed the recruitment of BRCA1 and B3BP1, which are key checkpoint proteins for HR and NHEJ repair, respectively. We found that the spike protein markedly inhibited both BRCA1 and B3BP1 foci formation. Together, these data show that the SARS-CoV-2 full-length spike protein inhibits DNA damage repair by hindering DNA repair protein recruitment."
These two gene mutations have been found to increase risk of cancer big time. (Quoting a separate study below):
"Women with germline BRCA1 and BRCA2 mutations have five- to 20-fold increased risks of developing breast and ovarian cancer."
On 53BP1 (53-binding-protein-1):
53BP1: A key player of DNA damage response with critical functions in cancer:
"It has been extensively demonstrated that aberrant expression of 53BP1 contributes to tumor occurrence and development. 53BP1 loss of function in tumor tissues is also related in tumor progression and poor prognosis in human malignancies."
(*aberrant = changed/altered)
Interestingly, if you look at the vaccine inserts for J&J, Pfizer and AstraZeneca you will find this (right from the FDA):
"COMIRNATY has NOT been evaluated for the potential to cause carcinogenicity, genotoxicity, or impairment of
male fertility."
In addition to this information, a study from Sweden of February this year proved that Pfizer vaccines alter DNA.
Intracellular Reverse Transcription of Pfizer BioNTech COVID-19 mRNA Vaccine BNT162b2 In Vitro in Human Liver Cell Line:
“In this study, we investigated the effect of BNT162b2 on the human liver cell line Huh7 in vitro,”
(*HuH-7, hereafter Huh7, is an immortal cell line built from male hepatoma tissue.)
(*BNT162b2 is a lipid nanoparticle–formulated, nucleoside-modified RNA vaccine that encodes a prefusion stabilized, membrane-anchored SARS-CoV-2 full-length spike protein.)
(*hepatoma tissue = cancer cells of the kidney.)
The study found that the mRNA injection is able to enter the human liver cell line Huh7 and that the injections’ mRNA is reverse transcribed into DNA as fast as SIX HOURS after the cells were exposed to it.
“A possible mechanism for reverse transcription is through endogenous [intracellular] reverse transcriptase LINE-1, and the nucleus protein distribution of LINE-1 is elevated by BNT162b2.”
LINE-1 is a reverse transcriptase that we carry and it comprises ≈17% of our genome.
“Our study shows that [Pfizer’s mRNA injection] … can be reverse transcribed to DNA … and this may give rise to the concern if [injection]-derived DNA may be integrated into the host genome and affect the integrity of genomic DNA, which may potentially mediate genotoxic side effects.”
Going through all this science stuff it makes me wonder how people are still standing and how long before these ticking time bombs go off full-scale. On top of all this you guys no doubt have seen the self-assembling nanotech that reacts to microwaves. The footage looks almost like it's from 30 years into the future. Crazy stuff.
Sources for information: NaturalNews.com, Bitchute.com
SARS-CoV-2 Spike Impares DNA Damage Repair and Inhibits V(D)J Recombination in Vitro:
"Here, by using an in vitro cell line, we report that the SARS-CoV-2 spike protein significantly inhibits DNA damage repair, which is required for effective V(D)J recombination in adaptive immunity. Mechanistically, we found that the spike protein localizes in the nucleus and inhibits DNA damage repair by impeding key DNA repair protein BRCA1 and 53BP1 recruitment to the damage site."
("V(D)J recombination is the mechanism of somatic recombination that occurs only in developing lymphocytes during the early stages of T and B cell maturation. It results in the highly diverse repertoire of antibodies/immunoglobulins and T cell receptors (TCRs) found in B cells and T cells, respectively. The process is a defining feature of the adaptive immune system." - Wikipedia)
It's important to understand these two pathways, Non-homogulous end joining (NHEJ) and Homologous Recombination (HR) as explained in another quote:
"NHEJ repair and holologus recombination repair are two major DNA repair pathways that not only continuously monitor and ensure genome integrity but are also vital for adaptive immune cell functions."
From study "Comparison of nonhomologous end joining and homologous recombination in human cells:"
"...we conclude than in proliferating cells NHEJ repairs 75% of DSBs while HR repairs the remaining 25%."
The scientists (from the first study mentioned) used DNA treatments on damaged cells and tested them for SARS-CoV-2 proteins. The spike protein (in both NHEJ and HR) had an efficiency rate of around 10% and 20%, which means it inhibits this repair mechanism by 80% to 90%. (See slide below).
"To determine how the spike protein inhibits both NHEJ and HR repair pathways, we analyzed the recruitment of BRCA1 and B3BP1, which are key checkpoint proteins for HR and NHEJ repair, respectively. We found that the spike protein markedly inhibited both BRCA1 and B3BP1 foci formation. Together, these data show that the SARS-CoV-2 full-length spike protein inhibits DNA damage repair by hindering DNA repair protein recruitment."
These two gene mutations have been found to increase risk of cancer big time. (Quoting a separate study below):
"Women with germline BRCA1 and BRCA2 mutations have five- to 20-fold increased risks of developing breast and ovarian cancer."
On 53BP1 (53-binding-protein-1):
53BP1: A key player of DNA damage response with critical functions in cancer:
"It has been extensively demonstrated that aberrant expression of 53BP1 contributes to tumor occurrence and development. 53BP1 loss of function in tumor tissues is also related in tumor progression and poor prognosis in human malignancies."
(*aberrant = changed/altered)
Interestingly, if you look at the vaccine inserts for J&J, Pfizer and AstraZeneca you will find this (right from the FDA):
"COMIRNATY has NOT been evaluated for the potential to cause carcinogenicity, genotoxicity, or impairment of
male fertility."
In addition to this information, a study from Sweden of February this year proved that Pfizer vaccines alter DNA.
Intracellular Reverse Transcription of Pfizer BioNTech COVID-19 mRNA Vaccine BNT162b2 In Vitro in Human Liver Cell Line:
“In this study, we investigated the effect of BNT162b2 on the human liver cell line Huh7 in vitro,”
(*HuH-7, hereafter Huh7, is an immortal cell line built from male hepatoma tissue.)
(*BNT162b2 is a lipid nanoparticle–formulated, nucleoside-modified RNA vaccine that encodes a prefusion stabilized, membrane-anchored SARS-CoV-2 full-length spike protein.)
(*hepatoma tissue = cancer cells of the kidney.)
The study found that the mRNA injection is able to enter the human liver cell line Huh7 and that the injections’ mRNA is reverse transcribed into DNA as fast as SIX HOURS after the cells were exposed to it.
“A possible mechanism for reverse transcription is through endogenous [intracellular] reverse transcriptase LINE-1, and the nucleus protein distribution of LINE-1 is elevated by BNT162b2.”
LINE-1 is a reverse transcriptase that we carry and it comprises ≈17% of our genome.
“Our study shows that [Pfizer’s mRNA injection] … can be reverse transcribed to DNA … and this may give rise to the concern if [injection]-derived DNA may be integrated into the host genome and affect the integrity of genomic DNA, which may potentially mediate genotoxic side effects.”
Going through all this science stuff it makes me wonder how people are still standing and how long before these ticking time bombs go off full-scale. On top of all this you guys no doubt have seen the self-assembling nanotech that reacts to microwaves. The footage looks almost like it's from 30 years into the future. Crazy stuff.
Sources for information: NaturalNews.com, Bitchute.com