How the covid experimental "vaccines" cause damage BY DESIGN
submitted 2 years ago * by zyxzevn from (self.VaccineSkepticism)
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[–]zyxzevn[S] 1 insightful - 1 fun1 insightful - 0 fun2 insightful - 0 fun2 insightful - 1 fun - 1 year ago* (1 child)
Mechanism of Covid-19 vaccine injury: https://iceni.substack.com/p/mechanisms-of-covid-19-vaccine-injury
(see original for full context and listing)
A Laundry List of Issues
Lipid Nanoparticles
Synthetic mRNA
[–]zyxzevn[S] 1 insightful - 1 fun1 insightful - 0 fun2 insightful - 0 fun2 insightful - 1 fun - 1 year ago* (0 children)
Poor Antibody Responses
Boosting of Cross-Reactive Antibodies to Endemic Coronaviruses by SARS-CoV-2 Infection but not Vaccination with Stabilized Spike - medRxiv (Preprint)
Anti-nucleocapsid antibodies following SARS-CoV-2 infection in the blinded phase of the mRNA-1273 Covid-19 vaccine efficacy clinical trial - medRxiv (Preprint)
Cleavage and Presence in Bloodstream
Circulating Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) Vaccine Antigen Detected in the Plasma of mRNA-1273 Vaccine Recipients - Clinical Infectious Diseases
Coagulopathy
Clinical Characteristics and Pharmacological Management of COVID-19 Vaccine–Induced Immune Thrombotic Thrombocytopenia With Cerebral Venous Sinus Thrombosis - JAMA
Coagulopathies after Vaccination against SARS-CoV-2 May Be Derived from a Combined Effect of SARS-CoV-2 Spike Protein and Adenovirus Vector-Triggered Signaling Pathways - MDPI
A central role for amyloid fibrin microclots in long COVID/PASC: origins and therapeutic implications - Portland Press Biochem Journal
Evidence of SARS-CoV-2 Spike protein on retrieved thrombi from COVID-19 patients - Research Square (Preprint)
Covid-19: European countries suspend use of Oxford-AstraZeneca vaccine after reports of blood clots - BMJ
Amyloidogenesis
SARS-CoV-2 spike protein interactions with amyloidogenic proteins: Potential clues to neurodegeneration - Elsevier
Amyloidogenesis of SARS-CoV-2 Spike Protein - ACS
Autoimmune Attack
Intravenous Injection of Coronavirus Disease 2019 (COVID-19) mRNA Vaccine Can Induce Acute Myopericarditis in Mouse Model - Clinical Infectious Diseases
Role of the antigen presentation process in the immunization mechanism of the genetic vaccines against COVID-19 and the need for biodistribution evaluations - Wiley
New-onset autoimmune phenomena post-COVID-19 vaccination - Wiley
Innate immune suppression by SARS-CoV-2 mRNA vaccinations: The role of G-quadruplexes, exosomes, and MicroRNAs - Elsevier
Auto-immune hepatitis following COVID vaccination - Elsevier
Autoimmune hepatitis after COVID-19 vaccine – more than a coincidence - Elsevier
SARS-CoV-2 vaccination can elicit a CD8 T-cell dominant hepatitis - Journal of Hepatology00234-3/fulltext)
Integrin Binding
A potential role for integrins in host cell entry by SARS-CoV-2 - Elsevier
Integrin mediates cell entry of the SARS-CoV-2 virus independent of cellular receptor ACE2 - JBC
ACE2-independent infection of T lymphocytes by SARS-CoV-2 - Signal Transduction and Targeted Therapy
Blood Brain Barrier Effects
SARS-CoV-2 Spike Protein Disrupts Blood–Brain Barrier Integrity via RhoA Activation - Springer
The SARS-CoV-2 spike protein alters barrier function in 2D static and 3D microfluidic in-vitro models of the human blood–brain barrier - Elsevier
The S1 protein of SARS-CoV-2 crosses the blood–brain barrier in mice - Nature
From the available data, our conclusions regarding the mRNA vaccines are as follows:
The PEGylated LNPs are capable of occasionally causing severe allergic reactions. The LNPs do not remain at the injection site, but travel all over the body and accumulate in key organs.
Unlike the virus, which only infects cells that express the host factors, LNPs can be endocytosed by practically any cell.
Synthetically-capped, pseudouridylated mRNA:
Resists breakdown by nucleases and may accumulate and persist over a long period of time.
May act as a TLR7/8 inhibitor.
May encourage stop codon readthrough and translate normally untranslated regions of the mRNA strand, resulting in an unknown product with unknown properties.
Pfizer’s vaccine, which contains mtRNR1 in its UTR, may promote mitochondrial toxicity and mitochondrial deafness if this UTR is translated, though this has never been confirmed.
May be taken up by LINE-1 retrotransposon activity and reverse-transcribed into DNA.
If this DNA expresses Spike, then the afflicted cell may express Spike continuously.
SARS-CoV-2 Spike produced by the vaccine can be cleaved by endogenous proteases, resulting in loose S1 entering the bloodstream.
This implies that proline substitution does not render the Spike inert.
SARS-CoV-2 Spike is:
Incredibly pro-coagulant and harmful to endothelial integrity.
Highly inflammatory, with a Superantigenic region.
The expression of Spike by healthy cells may provoke autoimmune attack. Any cell that expresses SARS-CoV-2 Spike after being transfected with mRNA may be destroyed by the immune system.
Inadvertent intravenous injection is very harmful and can cause myocarditis and profound heart scarring.
The vaccines may trigger autoimmune attacks on nervous tissue, leading to Bell’s Palsy or Guillain-Barré.
The vaccines may trigger autoimmune hepatitis.
The vaccines may affect fertility or fetus viability if they trigger autoimmune attack against germ cells or fetal tissues.
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[–]zyxzevn[S] 1 insightful - 1 fun1 insightful - 0 fun2 insightful - 0 fun2 insightful - 1 fun - (1 child)
[–]zyxzevn[S] 1 insightful - 1 fun1 insightful - 0 fun2 insightful - 0 fun2 insightful - 1 fun - (0 children)