Fauci admits that COVID-19 vaccines do not protect 'overly well' against infection
https://www.foxnews.com/media/fauci-admits-covid-19-vaccines-protect-overly-well-infection
So might catch BUT chance symptoms lessened
Your thoughts?View attachment 5014
Fauci admits that COVID-19 vaccines do not protect 'overly well' against infection
https://www.foxnews.com/media/fauci-admits-covid-19-vaccines-protect-overly-well-infection
So might catch BUT chance symptoms lessened
Your thoughts?
We have known all this for about a year now. Why is this presented as news? Is this just a way for deliberately stupid people to mount yet another misdirected attack on Fauci or something?
The vaccines have, from the start, never been very effective at preventing infection, but they are very, very good at reducing lessening the likelihood of severe disease and the duration of infection. This remains the case, even with the latest Omicron BA.4 and 5 variants. In the UK, lots of people are getting BA4 and 5 but few of them are getting anything more than a cold - and sometimes a bit of fever.
Don't you love "He is almost right."?
https://link.springer.com/article/10.1007/s41745-021-00268-8springer said:Antibody-Dependent Enhancement Phenomenon
Virus entry into host cells is a primary obligate process in viral pathogenesis; this is usually mediated by hijacking the cellular mechanism. Neutralizing antibodies aid in inhibiting the attachment of the virus to the host cell receptors by targeting the viral surface proteins or glycoproteins and is considered to be a crucial mechanism to eliminate the virus31,32,33,34,35,36, and the attachment between viruses and target cells plays an essential role in most cases and may produce different outcomes.
However, in some instances, paradoxically, binding of the antibodies at sub‐neutralizing concentrations to non-critical sites of the virion can result in non-neutralization of the virion that may lead to virion entry and invasion into certain cell types via antibody Fc region present on the carboxyl-terminal domain of antibody with Fc gamma receptor IIa (FcRIIa)-expressing phagocytic cells like the monocytes, macrophages, or through interaction with complement receptors contributing in the enhancement of infection, a process known as antibody-dependent enhancement37,38,39,40,41 during these instances, the binding of antibodies to these non-critical sites leaves the virus with retainment of its infectivity37.
Virus possesses various kinds of different antigenic epitopes capable of inducing neutralizing antibodies, but some might induce non-neutralizing antibodies that may enhance the infection42. Despite the presence of multiple critical sites on the virus surface, immunoglobulins, after attaching to this area, may not neutralize the virus completely because the virus can utilize another site for interacting with the host cell 37.
Diluting concentrations of antibodies have been shown to increase lung pathology and infiltration of cells into the alveolar air space observed in vivo mouse model during the influenza virus life cycles 43.
In an experimental study, it was observed that lower levels of IgG could promote the uptake of human parvovirus (B19V) in endothelial cells showing an enhancing effect of lower levels of antibodies at the level of virus internalization44. Seropositive people who may have successfully eliminated one viral serotype may well be at increased risk of infection with other viral serotypes. The neutralizing antibodies preformed for one of these serotypes might often not be neutralizing for different serotypes that may cross-neutralize the epitopes, and these deficient and incompetent neutralizing antibodies may instead allow ADE mechanism to kick in, leading to enhanced infection 45,46,47.
Dengue viruses, one of the best studied, representing a classic example of flaviviruses exhibiting ADE cause infection through four distinct serotypes DENV1, DENV2, DENV3, and DENV4; antibodies raised for one Dengue serotype do not protect against other serotypes failing to block the virus entry into cells42,48,49; the humoral response produced against one Dengue serotype provides protective serotype‐specific antibodies; however, these antibodies do cross‐react with other Dengue viral serotypes but do not neutralize them that may promote the entry of the virus via antibody Fc regions failing in protecting against different viral serotypes (Fig. 1); as a result, a second Dengue viral infection could arise, being more lethal, leading to dengue hemorrhagic fever and shock syndrome42,50, this similar instance of ADE can happen in COVID-19 in which RBD region of S protein of SARS-CoV-2 may get mutated as found in some studies51,52.
Enhancement of disease and more severity has been described in infants who received inactivated respiratory syncytial virus (RSV) vaccine as well as inactivated measles vaccine after they encountered a secondary viral infection53,54.
Me too. I only knew because I get antibody tests when I donate blood. But then again I have both vaccination and booster, so no suprise that it was mild.i have covid
Me too. I only knew because I get antibody tests when I donate blood. But then again I have both vaccination and booster, so no suprise that it was mild.
i was expecting to have caught it before now but i have not been testing.
household contacts tested after feeling symptoms so i tested.
otherwise i would not have known
i was due for a dentist appointment so its a bit of luck because i would not want to infect my dentist
was a debunker made up comment probabbly originating from homophobiaAnal probes
probing is ambiotic fluid through the stomach wall
which was reported before the procedure had been developed in modern science
- amniocentesis in abduction reports
Interesting. I would have thought along with amniocentesis aliens would have also run through a ultrasound
Description of a ultrasound before human had invented them would be almost definitively proof of aliens
yes there are reports of people being able to see their internal organs on a screen