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Urgent Covid Pfizer vaccine female infertility concerns: read The FULL Petition

 
Anonymous Coward
User ID: 29292321
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12/20/2020 05:01 AM
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just watch in the coming years and the birth rate plummets. do you think people will be able to make the connection
emerald eye  (OP)
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12/22/2020 11:31 PM

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Re: Urgent Covid Pfizer vaccine female infertility concerns: read The FULL Petition
Less than 50% quoted (emphasis mine):

“Suspicions grow that nanoparticles in Pfizer’s COVID-19 vaccine trigger rare allergic reaction”

Severe allergy-like reactions in at least eight people who received the COVID-19 vaccine produced by Pfizer and BioNTech over the past 2 weeks may be due to a compound in the packaging of the messenger RNA (mRNA) that forms the vaccine’s main ingredient, scientists say. A similar mRNA vaccine developed by Moderna, which was authorized for emergency use in the United States on Friday, also contains the compound, polyethylene glycol (PEG).”

PEG has never been used before in an approved vaccine, but it is found in many drugs that have occasionally triggered anaphylaxis—a potentially life-threatening reaction that can cause rashes, a plummeting blood pressure, shortness of breath, and a fast heartbeat. Some allergists and immunologists believe a small number of people previously exposed to PEG may have high levels of antibodies against PEG, putting them at risk of an anaphylactic reaction to the vaccine.”


The two vaccines both contain mRNA wrapped in lipid nanoparticles (LNPs) that help carry it to human cells but also act as an adjuvant, a vaccine ingredient that bolsters the immune response. The LNPs are “PEGylated”—chemically attached to PEG molecules that cover the outside of the particles and increase their stability and life span.”
“PEGs are also used in everyday products such as toothpaste and shampoo as thickeners, solvents, softeners, and moisture carriers, and they’ve been used as a laxative for decades. An increasing number of biopharmaceuticals include PEGylated compounds as well.”


“PEGs were long thought to be biologically inert, but a growing body of evidence suggests they are not. As much as 72% of people have at least some antibodies against PEGs, according to a 2016 study led by Samuel Lai, a pharmaco-engineer at the University of North Carolina, Chapel Hill, presumably as a result of exposure to cosmetics and pharmaceuticals. About 7% have a level that may be high enough to predispose them to anaphylactic reactions, he found. Other studies have also found antibodies against PEG, but at lower levels.”

This is consistent with the petition linked in this thread filed in the EU by the former Pfizer VP and German MD, as many as 70% of the population may have allergic reactions to PEGs (polyethylene glycols) and 7% may have potentially lethal anaphylactic reactions . Thus this represents a possible 7% death rate from the PEG containing vaccines, versus a fraction of a percentage death rate from the virus for most previously healthy people"

As always my posts are not intended as medical advice but presented merely for entertainment and free discussion purposes.hfhfhf

References:

[link to www.sciencemag.org (secure)]
[link to pubs.acs.org (secure)]

Last Edited by emerald eye on 12/22/2020 11:39 PM
Courage forges a path through all obstacles,
while fear is the obstruction of all dreams.


The only way that anyone gets something for nothing, is that someone else has given up something for nothing.
emerald eye  (OP)
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01/01/2021 10:33 AM

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Re: Urgent Covid Pfizer vaccine female infertility concerns: read The FULL Petition
Brandy Vaughan was found dead by her 10-year-old son on December 8, 2020. Rest in Peace....hfhfhf

She was a former Merck employee who well understood the profit without liability motivation of the pharmaceutical industry, especially with respect to vaccines, the lack of safety testing of vaccines, and the complete lack of any meaningful oversight or regulation.

She ran the website Learn the Risk dot org



[link to www.youtube.com (secure)]

Last Edited by emerald eye on 01/01/2021 10:52 AM
Courage forges a path through all obstacles,
while fear is the obstruction of all dreams.


The only way that anyone gets something for nothing, is that someone else has given up something for nothing.
emerald eye  (OP)
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01/01/2021 10:55 AM

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Re: Urgent Covid Pfizer vaccine female infertility concerns: read The FULL Petition
Brandy Vaughan was found dead by her 10-year-old son on December 8, 2020. Rest in Peace....hfhfhf

She was a former Merck employee who well understood the profit without liability motivation of the pharmaceutical industry, especially with respect to vaccines, the lack of safety testing of vaccines, and the complete lack of any meaningful oversight or regulation.

She ran the website Learn the Risk dot org



[link to www.youtube.com (secure)]
 Quoting: emerald eye


I guess free speech can and does get you killed these days...

Profit over People

verysad
Courage forges a path through all obstacles,
while fear is the obstruction of all dreams.


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Anonymous Coward
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01/05/2021 02:14 AM
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bump
emerald eye  (OP)
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01/10/2021 02:35 PM

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[link to www.youtube.com (secure)]

LOL!
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while fear is the obstruction of all dreams.


The only way that anyone gets something for nothing, is that someone else has given up something for nothing.
emerald eye  (OP)
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01/15/2021 11:10 AM

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Re: Urgent Covid Pfizer vaccine female infertility concerns: read The FULL Petition
I posted this on another thread but wanted to add it here:

I have very sad personal knowledge of a previously healthy late 30’s aged nurse who (this week) died within days after receiving her 2nd Covid 19 vaccine. She did not have any known underlying health issues and no previous major medical illnesses. She was strongly encouraged by her hospital employer to be vaccinated against SARS-CoV-2 (the causative virus of Covid 19 illness). She appeared to tolerate her first dose of the vaccine without incident. When she received her 2nd shot she did not feel well and continued to feel worse. Several days after the second vaccine dose she died at home before paramedics could get her to the hospital. The cause of death appears to be a massive amount of blood clots in both lungs and in her legs (PE, DVT).

Of course, the hospital is now saying her death was not related to the vaccine. However, if she had undergone surgery and died several days later, especially due to blood clots (PE or DVT), her death would have been classified as a surgical complication resulting in death, but magically with the same scenario, “her death cannot be a vaccine complication” because of some sort of distorted doublespeak thinking.

Her family and colleagues are all understandably devastated.

That is as much information as I can give without getting into trouble for a HIPPA violation. Somehow, everything is geared to keep us muzzled and to keep us from speaking the truth.

Think about this for a minute:

The mRNA platform is geared to cause the delivery of mRNA templates to code for your own protein transcription processes to make multiple copies of the SARS-CoV-2 (the Covid 19 virus) spike protein. Those copies of the spike protein will migrate to the surface of your cells in order to allow your body to make an antibody response to the spike protein. To accept that this is a safe platform; one must first believe that the SARS-CoV-2 spike protein itself is harmless. However, there is evidence that is not the case and that the spike protein itself is associated with thrombosis through the formation of abnormally fused cells:


“COVID-19 lung damage caused by persistence of 'abnormal cells”, November 4, 2020, King's College London

New research shows the SARS-CoV-2 virus' unique characteristics and may explain why patients suffer from 'long COVID'.

“Researchers analyzed the organs of 41 patients who died of COVID-19 at the University Hospital of Trieste, Italy, from February to April 2020, at the start of the pandemic. The team took lung, heart, liver, and kidney samples to examine the behavior of the virus.”

Almost 90% of patients showed two additional characteristics that were quite unique to COVID-19 compared to other forms of pneumonia. First, patients showed extensive blood clotting of the lung arteries and veins (thrombosis). Second, several lung cells were abnormally large and had many nuclei, resulting from the fusion of different cells into single large cells. This formation of fused cells (syncytia) is due to the viral spike protein, which the virus uses to enter the cell. When the protein is present on the surface of cells infected by the COVID-19 virus, it stimulates their fusion with other normal lung cells, which can be a cause for inflammation and thrombosis.”

[link to www.sciencedaily.com (secure)]


From the full article:
We attribute the high prevalence of these syncytial cells to the properties of the SARS-CoV-2 Spike protein. Both SARS-CoV and SARS-CoV-2 that bind the ACE2 receptor and can be activated by the TMPRSS2 protease. However, in the case of SARS-CoV, a main route for Spike activation follows endocytosis of the viral particles and is carried out by endosomal, low pH-activated proteases such as cathepsin B and cathepsin L. In contrast, other proteases, in particular furin, can prime SARS-CoV-2 Spike directly at the plasma membrane level, targeting a sequence at the S1/S2 interface that is not present in SARS-CoV As a consequence, cells expressing SARS-CoV-2 Spike can fuse with other cells expressing the ACE2 receptors and form syncytia, while this property is less pronounced for Spike from SARS-CoV.

The possible pathogenetic significance of this difference has remained so far unexplored. Of interest, mice transgenic for the DPP4 MERS-CoV receptor and infected with MERS-CoV develop pulmonary microvascular thrombosis. This observation might hint at the possibility that the fusogenic properties of the MERS-CoV- and SARS-CoV-2-infected cells might be linked to the pathogenesis of thrombosis. Further investigations are needed in this respect. In light of the persistence of virus-infected cells in the lungs of infected individuals and the peculiar molecular features of the SARS-CoV-2 Spike protein we propose that several of the clinical characteristics that set COVID-19 apart from other interstitial pneumonias are not attributable to pneumocyte death as a consequence viral replication, but to the persistence of virus-infected, Spike-expressing cells in the lungs of the infected individuals.


[link to www.thelancet.com (secure)]


The above is not for entertainment, as I am heartbroken, but it is for discussion. It is also not intended as medical advice; but I am tired of the lies and misrepresentation, the lack of critical thinking, and mostly the placing of pharmaceutical profits over human lives. I am just sick of it all.
verysad
Courage forges a path through all obstacles,
while fear is the obstruction of all dreams.


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emerald eye  (OP)
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01/15/2021 11:13 AM

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Re: Urgent Covid Pfizer vaccine female infertility concerns: read The FULL Petition
I also wanted to add my response to another poster on that thread from here:
(I didn't feel comfortable posting that person's post on my thread without permission, but it is linked below:

Thread: The Devastating Side Effects Of The Moderna Vaccine (Page 3)


My response:

You are obviously well versed in Chemistry and have some interesting thoughts, thanks for sharing them, especially about the LNP, I will follow up on that! (Chem was one of my majors as an undergrad and still a favorite, although I am quite rusty.)

The following quote pertains to your discussion about the observation of blood group O having less thrombosis risk from Covid. (If the spike proteins themselves cause thrombosis from interactions on the surface of the cell, either by creating abnormally large fused syncytia cells that cause thrombosis or by converting non-activator surfaces to activator surfaces; because of the following mechanisms, then type O blood group will be somewhat protected from run-away thrombosis).

Less than 50% quoted from all linked sources:

“Although ABO(H) blood group carbohydrate structures are traditionally considered red blood cell antigens, they are actually expressed on a range of other cell types, including endothelial cells (EC) and platelets. In addition, covalently linked ABO(H) determinants are also present on a number of plasma glycoproteins, including von Willebrand factor (VWF), and factor VIII (FVIII). Importantly, the ABO(H) sugars on VWF have been shown to influence its biological activity. First, plasma VWF levels are 20–30% lower in normal blood group O individuals compared to non-O subjects.

These reduced VWF levels are due to the fact that group O VWF has a significantly reduced plasma half-life compared to non-O VWF (10·0 compared to 25·5 h). Since FVIII circulates in high-affinity complex with VWF, plasma FVIII:C levels are also significantly reduced in blood group O individuals. Second, ABO(H) blood group determinants on VWF have also been shown to regulate susceptibility to proteolysis by ADAMTS13. In particular, group O VWF is cleaved significantly more rapidly by ADAMTS13 compared to non-O VWF. Finally, ABO sugars on both VWF and platelet GPIb have been demonstrated to influence VWF-dependent platelet aggregation under shear stress. Cumulatively, these ABO effects on VWF/FVIII and platelet biology undoubtedly play a major role in determining the reduced risk of thrombosis observed in blood group O subjects.”

[link to www.ncbi.nlm.nih.gov (secure)]

“Here, we demonstrate that the SARS-CoV-2 spike protein (subunit 1 and 2), but not the N protein, directly activates the alternative pathway of complement (APC). “
In conclusion, SARS-CoV-2 spike proteins convert nonactivator surfaces to activator surfaces by preventing the inactivation of the cell-surface APC convertase. APC activation may explain many of the clinical manifestations (microangiopathy, thrombocytopenia, renal injury, and thrombophilia) of COVID-19 that are also observed in other complement-driven diseases such as atypical hemolytic uremic syndrome and catastrophic antiphospholipid antibody syndrome. C5 inhibition prevents accumulation of C5b-9 in vitro but does not prevent upstream complement activation in response to SARS-CoV-2 spike proteins.”

[link to pubmed.ncbi.nlm.nih.gov (secure)]

This raises the specter that many of the thrombotic complications arising from SARS-CoV-2 infections may be triggered and/or exacerbated by excess complement activation. This is of major potential clinical relevance, as currently available anti-complement therapies that are highly effective in protecting against thrombosis in aHUS, could be efficacious in COVID-19. In this review, we provide mounting evidence for complement participating in the pathophysiology underlying the thrombotic diathesis associated with pathogenic coronaviruses, including SARS-CoV-2. Based on current knowledge of complement, coagulation and the virus, we suggest lines of study to identify novel therapeutic targets and the rationale for clinical trials with currently available anti-complement agents for COVID-19.”
[link to pubmed.ncbi.nlm.nih.gov (secure)]

In addition, there was co-localization of COVID-19 spike glycoproteins with C4d and C5b-9 in the interalveolar septa and the cutaneous microvasculature of 2 cases examined. In conclusion, at least a subset of sustained, severe COVID-19 may define a type of catastrophic microvascular injury syndrome mediated by activation of complement pathways and an associated procoagulant state.”

[link to pubmed.ncbi.nlm.nih.gov (secure)]

We have made a dangerous assumption that generating multiple copies of the spike protein to migrate to the surface of the cell is automatically safe because they “are not infectious” and only the spike protein.

I think there is evidence that the spike protein itself is capable of interacting on the cell surface in ways that aggravate thrombosis, particularly pulmonary thrombosis in potentially catastrophic ways.

I am convinced that the loss of a previously healthy thirty-something nurse days after her second Covid vaccine shot was a consequence of this.

Also, last night, I was working and one of the nurses (also young and previously healthy) got sent to the ED for stroke symptoms, difficulty speaking, a loss of strength on her left side, ect. I asked when she got her “2nd shot” and was told it was about a week ago, so some of the other nurses who had gotten the 2nd shot breathed a sigh of relief and thought this was once again just “bad-luck”. Stroke symptoms could also be a result of microvascular thrombosis in the brain.

If young healthy people are having thrombotic events, following the 2nd dose, then old folks don’t stand a chance. All of the blood clots, strokes, and heart attacks will just be classified as “bad-luck”.

The above is intended for entertainment and discussion, and not intended as medical advice. However, independent thinking is still strongly encouraged.

hfhfhf

Last Edited by emerald eye on 01/15/2021 11:13 AM
Courage forges a path through all obstacles,
while fear is the obstruction of all dreams.


The only way that anyone gets something for nothing, is that someone else has given up something for nothing.
emerald eye  (OP)
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03/08/2021 06:21 PM

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Re: Urgent Covid Pfizer vaccine female infertility concerns: read The FULL Petition
I posted this information on another thread, but thought I would also add it here:



There is now little debate that the Covid- 19 (SARS-C-CoV-2) infection causes damage to endothelial neurologic, and cardiac tissues above and aside from alveolar lung damage. As the alveolar tissues are rich in capillaries (tiny blood vessels), any type of endothelia damage seems now to be a universal pathology of this virus.


Many of the newer papers directly attribute this type of damage to the unique SARS-C-CoV-2 spike protein.

For example:


“SARS-CoV-2 Spike Protein Impairs Endothelial Function via Downregulation of ACE2”

“We show here that S(spike) protein alone can damage vascular endothelial cells (ECs) in vitro and in vivo, manifested by impaired mitochondrial function, decreased ACE2 expression and eNOS activity, and increased glycolysis. The underlying mechanism involves S protein downregulation of AMPK and upregulation of MDM2, causing ACE2 destabilization. Thus, the S(spike) protein-exerted vascular endothelial damage via ACE2 downregulation overrides the decreased virus infectivity.”

[link to www.biorxiv.org (secure)]


“SARS-CoV-2 Spike Proteins Disrupt the Blood-Brain Barrier, Potentially Raising Risk of Neurological Damage in COVID-19 Patients”

“New work by scientists at the Lewis Katz School of Medicine at Temple University shows that the spike proteins that extrude from SARS-CoV-2 promote inflammatory responses on the endothelial cells that form the blood-brain barrier. The study, published in the December print issue of the journal Neurobiology of Disease, is the first to show that SARS-CoV-2 spike proteins can cause this barrier to become “leaky,” potentially disrupting the delicate neural networks within the brain. “

[link to www.templehealth.org (secure)]


The SARS-CoV-2 spike protein disrupts the cooperative function of human cardiac pericytes -endothelial cells through CD147 receptor-mediated signaling: a potential non-infective mechanism of COVID-19 microvascular disease”


“We show, for the first time, that the recombinant S (spike) protein alone elicits functional alterations in cardiac PCs. This was documented as: (1) increased migration, (2) reduced ability to support EC network formation on Matrigel, (3) secretion of pro-inflammatory molecules typically involved in the cytokine storm, and (4) production of pro-apoptotic factors responsible for EC death. Furthermore, the S (spike) protein stimulates the phosphorylation/activation of the extracellular signal-regulated kinase 1/2 (ERK1/2) through the CD147 receptor, but not ACE2, in cardiac PCs. Accordingly, the neutralization of CD147, using a blocking antibody, prevented the activation of ERK1/2 and partially rescued the PC function in the presence of the S (spike) protein.”

"Interpretation. Our findings suggest the new, intriguing hypothesis that the S(spike)protein may elicit vascular cell dysfunction, potentially amplifying, or perpetuating, the damage caused by the whole coronavirus. This mechanism may have clinical and therapeutic implication.”

[link to www.biorxiv.org (secure)]



What do the currently used Covid- 19 (SARS-C-CoV-2) vaccines do?

They are engineered to create a large amount of spike protein in order to create an antibody response with no thought or concern to possible risks of the spike protein upon endothelial or other cells.

There is just a false assumption that creating large amounts of spike protein is safe just because it is not infectious; when the literature about the spike protein points to an opposite conclusion, the spike protein alone is capable of causing significant vascular and tissue damage. It’s similar to saying the bomb is harmless just because the factory in which it was made is no longer active.


Also, the problem of ADE (Antibody-Dependent Enhancement) was never been solved, preventing the development of vaccines for SARS in 2002 and MERS 2008 that could pass safety standards. ADE increased the risk of death in vaccinated as compared to unvaccinated animals due to cytokine storm upon re-infection, so even a traditional vaccine for SARS-C-CoV-2 carries this, as yet, unresolved risk.


As always, none of my posts are intended as medical advice and presented merely for the purposes of entertainment and discussion.hf
Courage forges a path through all obstacles,
while fear is the obstruction of all dreams.


The only way that anyone gets something for nothing, is that someone else has given up something for nothing.
Anonymous Coward
User ID: 73856390
Canada
03/08/2021 06:28 PM
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Re: Urgent Covid Pfizer vaccine female infertility concerns: read The FULL Petition
North America will be a farm colony

unless the people redpill and take action fast enough

go back to work

buy local

build a new, stronger north america

hustle or get wiped out
emerald eye  (OP)
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03/09/2021 10:23 AM

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Less than 50% quoted:

"Could Spike Protein in Moderna, Pfizer Vaccines Cause Blood Clots, Brain Inflammation, and Heart Attacks?

Dr. J. Patrick Whelan, a pediatric rheumatologist, warned the FDA in December that mRNA vaccines could cause microvascular injury to the brain, heart, liver and kidneys in ways not assessed in safety trials."


"If not viral infection, what else could be causing injury to distant organs associated with COVID-19?

The most likely culprit that has been identified is the COVID-19 spike protein released from the outer shell of the virus into circulation. Research cited below has documented that the viral spike protein is able to initiate a cascade of events that triggers damage to distant organs in COVID-19 patients.

Worryingly, several studies have found that the spike proteins alone have the capacity to cause widespread injury throughout the body, without any evidence of virus.

What makes this finding so disturbing is that the COVID-19 mRNA vaccines manufactured by Moderna and Pfizer and currently being administered throughout the U.S. program our cells to manufacture this same coronavirus spike protein as a way to trigger our bodies to produce antibodies to the virus.

According to Whelan’s letter to the FDA, the “Pfizer/BioNTech vaccine is composed of an mRNA that produces a membrane-anchored full-length spike protein.”

A landmark study in Nature Neuroscience, published a few days after Whelan’s letter, found that the commercially obtained COVID-19 spike protein (S1) injected into mice readily crossed the blood-brain barrier, was found in all 11 brain regions examined and entered the parenchymal brain space (the functional tissue in the brain)."

[link to childrenshealthdefense.org (secure)]

hfhfhf

Last Edited by emerald eye on 03/09/2021 10:27 AM
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while fear is the obstruction of all dreams.


The only way that anyone gets something for nothing, is that someone else has given up something for nothing.
emerald eye  (OP)
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04/22/2021 06:19 PM

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No matter what the current vaccine, they all produce the S or Spike protein, with recognized impacts that are cardiovascular, endothelial (blood vessel lining), and potential neurologic impacts with the penetration of the blood-brain barrier so it really doesn’t matter which one is given.

Also, ADE (Antibody Dependent Enhancement) was the reason the vaccines for the original SARS in 2002 and MERS in 2008 could never be developed because they failed the animal studies when there were increased deaths in vaccinated animals challenged with live virus versus unvaccinated animals (ADE). Guess what, to accomplish “warp-speed” the animal trials were skipped.

From the literature, less than 50% quoted, emphasis mine:

Evidence provided suggests that the SARS-CoV-2 spike proteins trigger a pro-inflammatory response on brain endothelial cells that may contribute to an altered state of BBB(Blood Brain Barrier) function. Together, these results are the first to show the direct impact that the SARS-CoV-2 spike protein could have on brain endothelial cells; thereby offering a plausible explanation for the neurological consequences seen in COVID-19 patients.”

[link to www.sciencedirect.com (secure)]

Findings We show, for the first time, that the recombinant S (Spike) protein alone elicits functional alterations in cardiac PCs. This was documented as: (1) increased migration, (2) reduced ability to support EC network formation on Matrigel, (3) secretion of pro-inflammatory molecules typically involved in the cytokine storm, and (4) production of pro-apoptotic factors responsible for EC(endothelial cell) death. Furthermore, the S (Spike) protein stimulates the phosphorylation/activation of the extracellular signal-regulated kinase 1/2 (ERK1/2) through the CD147 receptor, but not ACE2, in cardiac PCs. Accordingly, the neutralization of CD147, using a blocking antibody, prevented the activation of ERK1/2 and partially rescued the PC function in the presence of the S protein.”
Interpretation Our findings suggest the new, intriguing hypothesis that the S (Spike) protein may elicit vascular cell dysfunction, potentially amplifying, or perpetuating, the damage caused by the whole coronavirus. This mechanism may have clinical and therapeutic implications.”

[link to www.biorxiv.org (secure)]


Importantly, spike protein itself can activate endothelial responses, and for this, a cellular infection by the virus is not necessary. Taken that ACE2 is the only relevant receptor for the spike protein, further research is warranted to elucidate the underlying signaling pathway including the activity of protein kinases and transcription factors. Spike protein with a D614G mutation found in new virus variants can bind ACE2 better than that of the original variant.”

In conclusion, novel data with brain endothelial cells in 3D flow culture indicate that upregulation of ACE2 associates with increased SARS-CoV-2 spike protein binding and transcriptional cell activation. These effects can be mediated by the spike protein independently of cellular infection by the virus. This may involve direct cell activation via ACE2 or potentially via other accessory receptors or even activation of proinflammatory shedding enzymes. These different pathways may all contribute to the increased cardiovascular risk in COVID19 patients.”

[link to www.ahajournals.org (secure)]

“ADE is a phenomenon in which pre-existing non- or poorly neutralizing antibodies enhance the viral entry and replication in the host cell. ADE is more common in flaviviruses, especially in the dengue virus, which has four serotypes. It has been shown that when patients are infected with dengue virus for first time, specific neutralizing antibodies are produced. However, if they are later infected with a different serotype of dengue virus, the pre-existing antibodies from the previous infection do not have enough potency to neutralize the new virus, even though they can bind with the virus. These partially neutralizing antibodies help the virus to enter cells via an Fc-receptor (FcR)-mediated mechanism in addition to their natural entry route (Fig. 2 A). The antibody-bound viruses bind via the antibody Fc-domain to FcR expressed on the surface of several immune cells, leading to enhancement of the virus entry and replication (Katzelnick et al., 2017; Khandia et al., 2018). ADE has also been reported in other viruses like HIV, Ebola, HCV, and Zika ((Gorlani and Forthal, 2013; Meyer et al., 2008; Takada et al., 2001; Willey et al., 2011)."

“Vaccine-induced enhancement was first reported during the vaccine trial of RSV in 1969. In this trial, the administration of the formalin-inactivated vaccine RSV (FI-RSV) to naïve infants resulted in a much higher incidence rate of severe illness. It led to increased hospitalization in 80 % among vaccinated infants, compared to only 5% of the non-immunized infants (Kim et al., 1969). Unfortunately, two vaccinated infants also died because of enhanced RSV infections (Kim et al., 1969).”

“There are huge theoretical concerns of vaccine-induced ADE which can occur in several scenarios. It is possible that vaccine-induced antibodies against SARS-CoV-2 may bind to the virus without neutralizing it. Currently, mutations on the viral Spike protein have been found in circulating clinical SARS-CoV-2 strains (Korber et al., 2020; Lu et al., 2020). If this happens, the non-neutralizing antibodies could produce ADE effect and enhance the viral entry into cells (Garber, 2020; Iwasaki and Yang, 2020; Tetro, 2020; Ulrich et al., 2020). In addition, significant sequence variations between the spike proteins of SARS-CoV and SARS-CoV-2 may cause ADE (Tetro, 2020). Moreover, it is also possible that a future SARS-related (SARSr)-CoV causes ADE in patients vaccinated with SARS-CoV-2, if the future SARSr-CoV shows significant sequence variations from SARS-CoV-2. Furthermore, insufficient concentration of neutralizing Ab may also cause ADE (Renner et al., 2018; Wan et al., 2019). Given the fact that neutralizing antibodies declined rapidly in some of COVID-19 patients (Long et al., 2020; Seow et al., 2020), this latter scenario is more troublesome. Nevertheless, based on the knowledge from research on SARS-CoV, several vaccine trials are ongoing for SARS-CoV-2.”
[link to www.ncbi.nlm.nih.gov (secure)]

These are what are openly admitted to in the current literature about the spike protein the vaccines force you to make.
What is not admitted to; but equally plausible are the concerns about gene therapy, irreversible genomic impact, and autoimmune triggers.

As always, none of my postings is intended for medical information but presented for discussion and entertainment purposes.
Stay safe GLP!

hfhfhf
Courage forges a path through all obstacles,
while fear is the obstruction of all dreams.


The only way that anyone gets something for nothing, is that someone else has given up something for nothing.
emerald eye  (OP)
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08/14/2021 03:02 PM

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Update my Dr. Micheal Yeardon...



DR. MIKE YEADON, FORMER PFIZER VP
Vice President and Chief Scientist for Allergy and Respiratory illnesses research and development
, Pfizer

Later founded his own Biotech company which he sold for over 300 million Euros.
Not exactly an idiot…

Latest message:



Latest message:
Do not take, especially if you are pregnant this experimental, still
in clinical trials gene therapy!
He also mentions a possible comparison to thalidomide!
Anyone giving this drug to a pregnant woman is an absolute reckless
idiot!

Again, presented for entertainment and discussion purposes only
Courage forges a path through all obstacles,
while fear is the obstruction of all dreams.


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Asc4110

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08/26/2021 09:06 AM
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bump
Asc4110





GLP