Forbes Staff
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May 13, 2022,11:00am EDT
TOPLINE
Immunity against the omicron coronavirus variant fades rapidly after a second and third dose of Pfizer and BioNTech’s Covid-19 vaccine, according to peer reviewed research published in JAMA Network Open on Friday, a finding that could support rolling out additional booster shots to vulnerable people as the variant drives an uptick in new cases across the country.
KEY FACTS
Levels of omicron-specific “neutralizing” antibodies—which can target the virus and stop it from replicating—decline rapidly after a second and third dose of Pfizer’s shot, according to the Danish study of 128 people who had received two or three doses.
Antibody levels, which are associated with protection against infection and disease, fell within weeks of getting the shots and were much lower than the level of antibodies specific to the original and delta coronavirus variants, the researchers said.
Compared to original and delta variants, the proportion of omicron-specific antibodies detected in participants’ blood dropped “rapidly” from 76% four weeks after the second shot to 53% at weeks eight to 10 and 19% at weeks 12 to 14, the researchers found.
Omicron-specific antibody levels increased after the third dose—nearly 21-fold at week three and nearly 8-fold at week four, compared to four weeks after the second dose—and the shot generated a detectable response in most people for at least eight weeks, the researchers said.
However, antibody levels started to drop as early as three weeks after the booster shot, falling 4.9-fold for the original variant, 5.6-fold for delta and 5.4-fold for omicron between weeks three and eight.
The “transient” antibody response after doses two and three mean additional booster shots might be needed to combat the variant, particularly among older people, the researchers said.
KEY BACKGROUND
Experts and regulators broadly acknowledge the benefits of a third vaccine dose to top up flagging protection against serious illness and death. There is less consensus over whether additional shots are needed beyond that and questions over whether frequent boosting will be practical. Neutralizing antibodies have been the primary focus of studies evaluating vaccines—they are much easier to study—but they are not the only part of the immune system protecting humans against disease. Other parts of the immune system, such as T cells, might be less effective at preventing infection but they are more durable than antibodies and can reduce the chance of serious illness if infected. Many experts believe this latter property is the primary function of vaccination, not preventing infection, and data shows they offer much more durable protection, including against omicron.
FURTHER READING
We Cannot ‘Boost Our Way Out’ Of The Covid Pandemic, Experts Warn (Forbes)
Do You Need A Second Covid Booster Shot? Experts Are Divided. (Forbes)
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Spike Protein Protocol
Glutathione (most important for body detoxification) or better
NAC = N-Acetyl-Cysteine 600-750mg (causes the body to produce glutathione itself)
Zinc
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Alternatively CDS/CDL and zeolite
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INTELLIGENCE ISN’T KNOWING EVERYTHING, IT’S THE ABILITY TO CHALLENGE EVERYTHING YOU KNOW
Rights and Freedoms 
Who writes shit like this?
The vaccines don’t work, so we have to get more vaccines?
Here again the composition of the so-called vaccines.
There is not a single portion of a SARS-CoV-2 virus in the vaccines.
That is why these drugs are not vaccines.
There are billions of cold virus mRNA portions, from adenoviruses contained in every single shot. AstraZeneca uses cold viruses from monkeys. More specifically, from chimpanzees.
Because the human immune system cannot easily destroy chimpanzee adenoviruses.
PEG . Polyethylene glycol from vaccines is used to make polyester and is also found in antifreeze.
Polyethylene glycol is a component of many plastics that are not naturally degradable and are poisoning our oceans.
The spike proteins are mimics of the SARS-CoV-2 spike proteins in the laboratory.
They consist of a string of amino acids. These proteins are additionally reinforced with the amino acid proline. This alone distinguishes the copies from the original SARS-CoV-2 spike proteins and they are not exact replicas.
The adenoviruses are packaged in nanoparticles, which consist of 90 percent chemicals, mainly chemical lipids and polyethylene glycol.
Here again are the applications of polyethylene glycol.
Product
Description Properties Applications PEG 1500
CAS: 25322-68-3 Chemical name: Polyethylene glycol Appearance: Flakes Color: White pH: 4.5-7.0 (5% in water) Water soluble polymer produced by polymerization of ethylene oxide. Source: https://www.impag.de/material-science/industrial-chemicals/produkte/polyethylenglycol-peg-fest
Kinetic viscosity: 50-58 (20°C, 50% aqueous solution) Hydroxyl value: Approx. 65-75mg KOH/g Detergent and cleaning agent Lubricant and mold release agent Plasticizer and binder for ceramic molding compounds Rubber / plastic production Plastics / polyester, polyurethanes Additive for fibers, textiles and leather processing Paint industry Metal processing Paper and packaging industry Wood industry.
Healthy alternatives:
Andrographis against SARS-CoV-2
Source: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7212536/
Or this example:
Drosten’s 2020 study on the successful treatment of SARS-CoV-2 viruses with spermidine and spermine.
https://www.biorxiv.org/content/10.1101/2020.04.15.997254v1.full
Analysis of SARS-CoV-2-controlled autophagy reveals spermidine, MK-2206, and niclosamide as putative antiviral therapeutics
Nils C. Gassen, Jan Papies, Thomas Bajaj, Frederik Dethloff, Jackson Emanuel, Katja Weckmann, Daniel E. Heinz, Nicolas Heinemann, Martina Lennarz, Anja Richter, Daniela Niemeyer, Victor M. Corman, Patrick Giavalisco,
Christian Drosten, Marcel A. Müller
doi: https://doi.org/10.1101/2020.04.15.997254
Now published in Nature Communications doi: 10.1038/s41467-021-24007-w
Safe alternatives to the toxic vaccines do not seem to play a role in the treatment of SARS-CoV-2.
And here is another important aspect, why it is better not to get this poison mixture from Pfizer and co injected into the healthy cells.
The question about SARS-CoV-2 vaccines is not whether SARS-CoV-2 vaccines are toxic. There is now countless, irrefutable evidence of that.
The question must be why are politicians around the world poisoning the population with chemicals that are not vaccines, even though every member of parliament is now aware of the toxicity of the SARS-CoV-2 vaccines.
Here is an original excerpt from the Pfizer study that Pfizer was forced to release because of a court ruling in Texas. None of the reported side effects were mentioned within the study.
Anyone who continues to administer or supports the administration of the SARS-CoV-2 vaccines is supporting the largest mass murder in the history of the world.
What we are witnessing right now is a regular systematic and detailed planned worldwide execution of millions of healthy people.
Here are Pfizer’s concealed findings on possible side effects associated with the SARS-CoV-2 vaccines.
Cumulative analysis of post-approval adverse event reports.
APPENDIX 1. LIST OF ADVERSE EVENTS OF SPECIAL INTEREST
I am copying you here only the adverse possible side effects with the letter A because otherwise it will be Too Much. You can read the rest yourself via the link in the Pfizer PDF at the end of the study.
Click to access 5.3.6-postmarketing-experience.pdf
APPENDIX 1. LIST OF ADVERSE EVENTS OF SPECIAL INTEREST
1p36 deletion syndrome;2-Hydroxyglutaric aciduria;5’nucleotidase increased;Acoustic neuritis;Acquired C1 inhibitor deficiency;Acquired epidermolysis bullosa;Acquired epileptic aphasia;Acute cutaneous lupus erythematosus;Acute disseminated encephalomyelitis;Acute encephalitis with refractory, repetitive partial seizures;Acute febrile neutrophilic dermatosis;Acute flaccid myelitis;Acute haemorrhagic leukoencephalitis;Acute haemorrhagic oedema of infancy;Acute kidney injury;Acute macular outer retinopathy;Acute motor axonal neuropathy;Acute motor-sensory axonal neuropathy;Acute myocardial infarction;Acute respiratory distress syndrome;Acute respiratory failure;Addison’s disease;Administration site thrombosis;Administration site vasculitis;Adrenal thrombosis;Adverse event following immunisation;Ageusia;Agranulocytosis;Air embolism;Alanine aminotransferase abnormal;Alanine aminotransferase increased;Alcoholic seizure;Allergic bronchopulmonary mycosis;Allergic oedema;Alloimmune hepatitis;Alopecia areata;Alpers disease;Alveolar proteinosis;Ammonia abnormal;Ammonia increased;Amniotic cavity infection;Amygdalohippocampectomy;Amyloid arthropathy;Amyloidosis;Amyloidosis senile;Anaphylactic reaction;Anaphylactic shock;Anaphylactic transfusion reaction;Anaphylactoid reaction;Anaphylactoid shock;Anaphylactoid syndrome of pregnancy;Angioedema;Angiopathic neuropathy;Ankylosing spondylitis;Anosmia;Antiacetylcholine receptor antibody positive;Anti-actin antibody positive;Anti-aquaporin-4 antibody positive;Anti-basal ganglia antibody positive;Anti-cyclic citrullinated peptide antibody positive;Anti-epithelial antibody positive;Anti-erythrocyte antibody positive;Anti-exosome complex antibody positive;Anti- GAD antibody negative;Anti-GAD antibody positive;Anti-ganglioside antibody positive;Antigliadin antibody positive;Anti-glomerular basement membrane antibody positive;Anti-glomerular basement membrane disease;Anti-glycyl-tRNA synthetase antibody positive;Anti-HLA antibody test positive;Anti-IA2 antibody positive;Anti-insulin antibody increased;Anti-insulin antibody positive;Anti-insulin receptor antibody increased;Anti- insulin receptor antibody positive;Anti-interferon antibody negative;Anti-interferon antibody positive;Anti-islet cell antibody positive;Antimitochondrial antibody positive;Anti-muscle specific kinase antibody positive;Anti-myelin-associated glycoprotein antibodies positive;Anti-myelin-associated glycoprotein associated polyneuropathy;Antimyocardial antibody positive;Anti-neuronal antibody positive;Antineutrophil cytoplasmic antibody increased;Antineutrophil cytoplasmic antibody positive;Anti-neutrophil cytoplasmic antibody positive vasculitis;Anti-NMDA antibody positive;Antinuclear antibody increased;Antinuclear antibody positive;Antiphospholipid antibodies positive;Antiphospholipid syndrome;Anti-platelet antibody positive;Anti-prothrombin antibody positive;Antiribosomal P antibody positive;Anti-RNA polymerase III antibody positive;Anti-saccharomyces cerevisiae antibody test positive;Anti-sperm antibody positive;Anti-SRP antibody positive;Antisynthetase syndrome;Anti-thyroid antibody positive;Anti-transglutaminase antibody increased;Anti-VGCC antibody positive;Anti- VGKC antibody positive;Anti-vimentin antibody positive;Antiviral prophylaxis;Antiviral treatment;Anti-zinc transporter 8 antibody positive;Aortic embolus;Aortic thrombosis;Aortitis;Aplasia pure red cell;Aplastic anaemia;Application site thrombosis;Application site vasculitis;Arrhythmia;Arterial bypass occlusion;Arterial bypass thrombosis;Arterial thrombosis;Arteriovenous fistula thrombosis;Arteriovenous graft site stenosis;Arteriovenous graft thrombosis;Arteritis;Arteritis
CONFIDENTIAL Page 1
FDA-CBER-2021-5683-0000083
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090177e196ea1800\Approved\Approved On: 30-Apr-2021 09:26 (GMT)
BNT162b2
5.3.6 Cumulative Analysis of Post-authorization Adverse Event Reports
Anyone who still recommends SARS-CoV-2 vaccination after all this knowledge should first be booted 2 times and then jailed.
We are definitely governed by sick and perverted neo-fascists who are working worldwide to reduce the world population with lethal injections. SARS-CoV-2 vaccines are the Zyklon B of these global mass murderers.
The difference with Hitler’s mass murder is that this time the genocide by Scholz, Merkel, Obama, Trudeau, Biden, Macron and all the other neo-fascist heads of government is not only the Jewish population, but the entire population of the Western world.
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