Spike - jab vs virus

Many people ask, what's the difference between the "vaccine" Spike and the spike from the virus

Spike - jab vs virus

All natural, endogenously produced messenger ribonucleic acid is a single-stranded molecule of RNA that corresponds to the genetic sequence of a gene and is NOT the same thing as a chemically modified mRNA that uses a technology platform for creation

mRNA manufacturing

Ever heard of:

codon reading errors,
polynucleotide fragmentation,
manufacturering quality control issues,
changes in MicroRNA signaling,
Important gene regulation (p53, BRCA, etc)
Endotoxin & anaphylaxis risks,
SV 40 promoter & cancer risks,
antibiotic resistance risks,
biodistribution of LNPs,
N1-methylpseudouridine substituted for uracils or
dsDNA plasmid contamination?

What about:
polydispersity,
lipid adducts,
tetrahydrofuran,
exosomal communication,
zeta charge,
nitrosamines,
metal contamination,
LNP size,
dispersion stability


The mRNA vaccines are made in massive vats of E.Coli bacteria (which is the primary constituent of poop)



You can have the most perfectly designed product, but there is no guarantee that is what will be the end result

Some questions:  Why do you bio-engineer a prefusion Spike protein if you are artificially creating the protein in the ribosome to be released to the cytosol to encounter the proteasome who job it is to degrade foreign proteins?  How much makes it out of the proteasome?


Uracil substituted with N1-methylpseudouridine causes ribosomal pausing, protein misfolding, extended synthesis and genesis of all kinds of proteins, not just prefusion spike proteins



The jab has mRNA strands that code for an 'altered' spike protein.
These are enveloped in a PEGylated lipid nanoparticle (LNP) that spreads into cells ALL OVER THE BODY.
They transfect everything. This is fundamentally very different from the spike from the virus.

Makes cells all over the body produce profuse quantities of cytotoxic, fusogenic spike proteins

These jab induced spikes behave differently from the viral spike protein found on SARS-CoV2 which only binds to certain receptors (such as ACE2, CD147, VEGF-A, nAChR) in a certain subset of cells



After a jab, you may be high in ALL of these biomarkers on a Blood/Urine Environmental Toxins Test

hs-CRP - high sensitivity cardio reactive protein - evaluates myocardial infarction, stroke, sudden cardiac death, etc

Homocysteine - amino acid which can be a signal for heart disease

High liver enzymes - signal of inflammation

GgT - Gamma-glutamyl Transferase - elevated levels are linked to a wide range of diseases

NT-proBNP - B-type natriuretic peptide (BNP) is a hormone produced by the heart. N-terminal (NT) pro hormone BNP. High levels in the blood indicate potential heart failure.

Myeloperoxidase (MPO) - shows that blood vessels have become inflamed. Also indicates autoimmune vasculitis diseases characterized by inflammation and necrosis of blood vessels.

PLAC - blood test used to measure serum activity of lipoprotein associated phospholipase. This enzyme is present when vascular walls breakdown. Shows individuals may be about to have a stroke, cardio disease or heart attack

HEMA - urine test that detects carcinogens, such as the ethylene oxide nanoparticles that are broken down from the polyethylene glycol hydrogel in the shots.

FCS man made
https://www.frontiersin.org/articles/10.3389/fviro.2022.834808/full

Jabbed vs Unjabbed study - childhood vaccines
https://ipaknowledge.org/ipak-vaxxed-v-unvaxxed-study.php?s=09

The vaccinated are driving the acquisition of spike protein mutations
https://www.medrxiv.org/content/10.1101/2021.07.29.21261006v1


despite full vaccination and universal masking of HCW, breakthrough infections occurred in 24 of 29
https://www.eurosurveillance.org/content/10.2807/1560-7917.ES.2021.26.30.2100636

Shedding of infectious SARS-CoV-2, despite vaccination
https://www.medrxiv.org/content/10.1101/2021.07.31.21261387v4


Exosomes with Spike protein are detected 4 Months post jab.
https://pubmed.ncbi.nlm.nih.gov/34654691/?s=09

vaccinees less protected against newly emerging variants.
https://pubmed.ncbi.nlm.nih.gov/33532796/


Convergent antibody responses to the SARS-CoV-2 spike protein in convalescent and vaccinated individuals
https://www.cell.com/cell-reports/fulltext/S2211-1247(21)01042-1

Vaccinated people are 13x more likely to get infected than those with natural immunity.
This study demonstrated that natural immunity confers longer lasting and stronger protection against infection, symptomatic disease AND hospitalization caused by the Delta variant compared to the Pfizer vaccine-induced immunity
https://www.medrxiv.org/content/10.1101/2021.08.24.21262415v1

Natural immunity is 27 times better
https://www.medrxiv.org/content/10.1101/2021.08.24.21262415v1

Natural immunity
http://web.archive.org/web/20220712133631/https://threadreaderapp.com/thread/1546842939086733317.html

15 studies that show natural immunity is far superior
https://www.theblaze.com/amp/horowitz-15-studies-that-indicate-natural-immunity-from-prior-infection-is-more-robust-than-the-covid-vaccines-2654789339?__twitter_impression=true

Natural immunity gives long lasting protection
https://www.nature.com/articles/s41586-021-03647-4

T cell memory still strong at 12 months
https://www.biorxiv.org/content/10.1101/2021.08.11.455984v1


So, let's clarify that T cells arise from hematopoietic stem cells, in the bone marrow, then migrate to the thymus gland to mature.

👉T cells mature into 3 distinct types of T cells:

👉CD8 + "killer" T cells,

👉CD4 + "helper" T cells,

and 👉"suppressor" or regulatory T cells.

➡️CD8 + "killer" T cells are cytotoxic, which means they are able to directly kill virus-infected cells, or cancer cells.

➡️CD4 + "helper" T cells are "auxiliary cells" and work by indirectly killing cells identified as foreign; they are also important because they directly affect B cells and, indirectly, other cell populations.

➡️"Regulatory" or suppressor T cells provide the critical tolerance mechanism, whereby they are able to distinguish invading cells from themselves, thus preventing immune cells from reacting inappropriately against their own cells (autoimmune response).

The optimal response, based on the stimulation of CD8 + T cells, is based on the signaling of CD4 + cells, the latter useful in the initial antigenic activation of CD8 T cells themselves and in the maintenance of memory CD8 + T cells, following a acute infection.

➡️The first signal is provided by the binding of the T cell receptor to its cognate peptide, antigen presenting cells, such as: 👉dendritic cells, 👉B cells, and 👉macrophages.

➡️The second signal comes from co-stimulation, usually products of pathogens, but sometimes products of cell degradation, such as necrotic bodies or heat shock proteins.

➡️(The only costimulatory receptor constitutively expressed by T cells = is CD28).

➡️This second signal authorizes the T cell to respond to an antigen. Without it, the T cell becomes more difficult to activate in the future.

➡️Once a T cell has been properly activated (it has received the 👉signal one and the 👉signal two) it alters its expression on the cell surface with a variety of proteins.

🎯Here's the reason why mRNA does NOT activate T cells, because it fails to trigger the 2 activation signals!

➡️It is very important to underline that activated T cells also change their cell surface glycosylation profile.

➡️The actual T cell receptor is composed of two separate peptide chains, which are produced by the independent T cell receptor genes, alpha and beta, (TCRα and TCRβ).

➡️T cells can be phosphorylated by CD28 proteins (and can also phosphorylate tyrosines onto many other molecules) which allows for the aggregation of signaling complexes around these proteins.


There is also a "technical" reason why the "vaccinated" still get infected is due to a mistake in choosing the type of vaccine.

These are not "traditional" (ie inactivated) vaccines.

Actually, as you know, these are gene therapy vaccines, so what is written, in the short mRNA sequence, covers a short Spike antigenic sequence
peak (purified by the way, so it's not even Wuhan original Spike "wild") which induces a rewrite, in the host's immune system, which is stimulated to produce antibodies.

Antibodies are a class of serum glycoproteins, globular proteins involved in the immune response (in the fight against the microorganisms considered
foreigner); these immunoglobulins are secreted by mature B lymphocytes (which host them in their cell membrane), while T lymphocytes are not involved.
Only T lymphocytes develop humoral and cellular immunity against any pathogen.

These "Vaccines" specifically add to selection pressure on Spike of Sars CoV 2 thus leading to immune escape variants. Never ending cycle

Also, you're actually much more likely to get Covid from someone who has been vaccinated than you are from someone who has recovered from a natural infection.

The mucosal surfaces represent the largest area of exposure of the body to external pathogens. Immunoglobulin A (IgA), in its secretory form, is the main effector of the mucosal immune system and provides an important first line of defense against most pathogens that invade the body at a mucosal surface. This is where viruses replicate (nose, throat, upper respiratory)
For someone who has had a natural infection, they have mucosal immunity and therefore carry no viral load in their mucosal membranes and DO NOT spread the disease.

The vaccinated however, DO NOT have mucosal immunity. The vaccine induced IgG antibodies are in the blood only.

The vaccinated can carry 251 times the viral load and spread MUCH more infection than ANYBODY else. If you want to demonize someone, it's the "vaccinated".. They're the ones spreading around the virus and CAUSING the variants

Viral loads 251 times higher in vaccinated
https://papers.ssrn.com/sol3/papers.cfm?abstract_id=3897733

New variants are completely resistant to the vaccines with the original spike
https://www.biorxiv.org/content/10.1101/2021.08.22.457114v1

Imperfect vaccinations can lead to highly virulent strains
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4516275/

Natural immunity gives long lasting protection
https://www.nature.com/articles/s41586-021-03647-4

T cell memory still strong at 12 months
https://www.biorxiv.org/content/10.1101/2021.08.11.455984v1

CDC admits natural immunity is far superior than vaccines
https://www.cdc.gov/mmwr/volumes/71/wr/mm7104e1.htm?s_cid=mm7104e1_w


Role of IgA in Covid-19
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7245198/

ALSO, the "vaccine" DOESN'T prevent infection or transmission.
Everyone knows this.