both in cause and outcome....
The studies are embedded in the article... can't wait for the circle jerk to shoot the messenger.
www.conservativewoman.co.uk
The Money Quotes:
Review of other studies: "Researchers have reported that the SARS-CoV-2 mRNA-LNP vaccine may pose the risk of development and progression of cancer [25-28]. In addition, several case reports have described cancer developing or worsening after vaccination and discussed possible causal links between cancer and mRNA-LNP vaccination [29-34]."
The mechanism for the impairment of the immune system: "Based on the molecular weight of BNT162b2 mRNA (Pfizer-BioNTech), the mRNA content per dose is estimated at 13 trillion molecules and 40 trillion molecules in mRNA-1273 (Moderna) [35,36]. The total number of cells in humans is estimated to be 37.2 trillion [37], making the number of mRNA-LNPs very high, ranging from one-third to the equivalent of the total cell number. After inoculation, the mRNA-LNPs are delivered to various organs, especially the liver, spleen, adrenal gland, ovary, and bone marrow [38]. In one study, vaccine mRNA was detected in the lymph nodes of persons vaccinated with hybridization of a SARS-CoV-2 mRNA vaccine-specific probe 7 to 60 days after the second mRNA-1273 or BNT162b2 dose [39]. Modified mRNA with N1-methyl-pseudouridine could translate a large amount of SARS-CoV-2 spike protein (S-protein) [40]. S-protein emerged on the surface of exosomes in the blood of the vaccinated [41]. Fragments of vaccine-specific recombinant S-protein were found in blood specimens of 50% of vaccine recipients and were still detected three to six months later [42]."
The more your vaxed the worse your immune system and the more susceptible to infection you are: "A study of more than 50,000 employees at a medical institution in the United States observed the incidence of the Omicron variant epidemic based on the number of vaccine doses received (0, 1, 2, 3, and 4 or more doses) over a period of 26 weeks and showed that the number of vaccines received was positively correlated with the cumulative incidence rate of COVID-19 [46]. Susceptibility to COVID-19 infection after multiple vaccinations may be enhanced by antibody-dependent enhancement [47], immune imprinting [39,48], and immunosuppression [25-27]. This can result in a risk of exposure to viral S-protein in addition to vaccine S-protein for the multiple-vaccinated. These data suggest a significant impact on vaccine recipients, including the large number of mRNA-LNPs that are injected, their rapid and widespread distribution particularly into specific organs, the amount of S-protein produced, its long persistence in the body, and increased susceptibility to infection. "
Increased risk of thrombosis: "Because cancer often leads to the activation of coagulation via various mechanisms, one of the major causes of mortality in patients with cancer is cancer-associated thrombosis (CAT) [49-51], manifesting as disseminated intravascular coagulation (DIC) in its most extreme form [52]. Therefore, it is reasonable to assume that the additional thrombus-forming tendency noted with the mRNA-LNP vaccine could be extremely dangerous. The viral and vaccine S-protein of SARS-CoV-2, especially Omicron lineages, having a solid electro-positive potential, could attach to electro-negative glycoconjugates on the surfaces of red blood cells (RBCs), other blood cells, and endothelial cells [53]. The S-protein of SARS-CoV-2 alone has been reported to bind to angiotensin-converting enzyme 2 (ACE2) and activate angiotensin II receptor type 1 (AT1) signal, which promotes interleukin-6 (IL-6) trans-signaling [54], induces vascular wall thickening via activation of the protein kinases [55], impairs mitochondrial function [56], and generates reactive oxygen species (ROS) [57]. A recent study revealed that certain segments of the S-protein can induce the formation of amyloid, a fibrous protein that is insoluble in water. This protein plays a significant role in blood coagulation and fibrinolytic disorders [58]. Anti-spike protein antibodies bind to the S-proteins that emerge on cell surfaces, which triggers autoimmune inflammatory reactions [59-63]. In addition, the injection of LNPs into mice has been reported to cause strong inflammation [64]. All these findings suggest that the COVID-19 mRNA-LNP vaccine poses a risk of thrombosis in individuals with cancer and might explain the excess mortalities after mass vaccination."
The studies are embedded in the article... can't wait for the circle jerk to shoot the messenger.
Massive cancer deaths study vindicates my warnings over covid boosters - The Conservative Woman
Massive cancer deaths study vindicates my warnings over covid boosters
www.conservativewoman.co.uk
The Money Quotes:
Review of other studies: "Researchers have reported that the SARS-CoV-2 mRNA-LNP vaccine may pose the risk of development and progression of cancer [25-28]. In addition, several case reports have described cancer developing or worsening after vaccination and discussed possible causal links between cancer and mRNA-LNP vaccination [29-34]."
The mechanism for the impairment of the immune system: "Based on the molecular weight of BNT162b2 mRNA (Pfizer-BioNTech), the mRNA content per dose is estimated at 13 trillion molecules and 40 trillion molecules in mRNA-1273 (Moderna) [35,36]. The total number of cells in humans is estimated to be 37.2 trillion [37], making the number of mRNA-LNPs very high, ranging from one-third to the equivalent of the total cell number. After inoculation, the mRNA-LNPs are delivered to various organs, especially the liver, spleen, adrenal gland, ovary, and bone marrow [38]. In one study, vaccine mRNA was detected in the lymph nodes of persons vaccinated with hybridization of a SARS-CoV-2 mRNA vaccine-specific probe 7 to 60 days after the second mRNA-1273 or BNT162b2 dose [39]. Modified mRNA with N1-methyl-pseudouridine could translate a large amount of SARS-CoV-2 spike protein (S-protein) [40]. S-protein emerged on the surface of exosomes in the blood of the vaccinated [41]. Fragments of vaccine-specific recombinant S-protein were found in blood specimens of 50% of vaccine recipients and were still detected three to six months later [42]."
The more your vaxed the worse your immune system and the more susceptible to infection you are: "A study of more than 50,000 employees at a medical institution in the United States observed the incidence of the Omicron variant epidemic based on the number of vaccine doses received (0, 1, 2, 3, and 4 or more doses) over a period of 26 weeks and showed that the number of vaccines received was positively correlated with the cumulative incidence rate of COVID-19 [46]. Susceptibility to COVID-19 infection after multiple vaccinations may be enhanced by antibody-dependent enhancement [47], immune imprinting [39,48], and immunosuppression [25-27]. This can result in a risk of exposure to viral S-protein in addition to vaccine S-protein for the multiple-vaccinated. These data suggest a significant impact on vaccine recipients, including the large number of mRNA-LNPs that are injected, their rapid and widespread distribution particularly into specific organs, the amount of S-protein produced, its long persistence in the body, and increased susceptibility to infection. "
Increased risk of thrombosis: "Because cancer often leads to the activation of coagulation via various mechanisms, one of the major causes of mortality in patients with cancer is cancer-associated thrombosis (CAT) [49-51], manifesting as disseminated intravascular coagulation (DIC) in its most extreme form [52]. Therefore, it is reasonable to assume that the additional thrombus-forming tendency noted with the mRNA-LNP vaccine could be extremely dangerous. The viral and vaccine S-protein of SARS-CoV-2, especially Omicron lineages, having a solid electro-positive potential, could attach to electro-negative glycoconjugates on the surfaces of red blood cells (RBCs), other blood cells, and endothelial cells [53]. The S-protein of SARS-CoV-2 alone has been reported to bind to angiotensin-converting enzyme 2 (ACE2) and activate angiotensin II receptor type 1 (AT1) signal, which promotes interleukin-6 (IL-6) trans-signaling [54], induces vascular wall thickening via activation of the protein kinases [55], impairs mitochondrial function [56], and generates reactive oxygen species (ROS) [57]. A recent study revealed that certain segments of the S-protein can induce the formation of amyloid, a fibrous protein that is insoluble in water. This protein plays a significant role in blood coagulation and fibrinolytic disorders [58]. Anti-spike protein antibodies bind to the S-proteins that emerge on cell surfaces, which triggers autoimmune inflammatory reactions [59-63]. In addition, the injection of LNPs into mice has been reported to cause strong inflammation [64]. All these findings suggest that the COVID-19 mRNA-LNP vaccine poses a risk of thrombosis in individuals with cancer and might explain the excess mortalities after mass vaccination."
