A vaxxed vs unvaxxed tale
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Never tested never took the shot never cared
Pussies
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The science was that this was an untested "vax" The science also said that the chicom crud was not a serious risk to healthy people under 40 and in particular to children. But you leftards don't do science. Everyone is the same. Everyone needs to be treated the same except for dem elites who went on vacation to Florida after locking there states down, or heading for a private beauty appointment or to the local blm/antifa riot.
Fauci on mucosal infections and vaccine effectiveness. Basically reiterating much of the Great Barrington Declaration which he wanted and got censured. Use on targeted groups and don't lie that if you take the mRNA experimental vax you can't get covid or spread covid. Then take in the horrific adverse event reports on the mRNA vaxxes
https://www.cell.com/cell-host-microbe/fulltext/S1931-3128(22)00572-8?_returnURL=https%3A%2F%2Flinkinghub.elsevier.com%2Fretrieve%2Fpii%2FS1931312822005728%3Fshowall%3Dtrue
Summary
Viruses that replicate in the human respiratory mucosa without infecting systemically, including influenza A, SARS-CoV-2, endemic coronaviruses, RSV, and many other “common cold” viruses, cause significant mortality and morbidity and are important public health concerns. Because these viruses generally do not elicit complete and durable protective immunity by themselves, they have not to date been effectively controlled by licensed or experimental vaccines. In this review, we examine challenges that have impeded development of effective mucosal respiratory vaccines, emphasizing that all of these viruses replicate extremely rapidly in the surface epithelium and are quickly transmitted to other hosts, within a narrow window of time before adaptive immune responses are fully marshaled. We discuss possible approaches to developing next-generation vaccines against these viruses, in consideration of several variables such as vaccine antigen configuration, dose and adjuventation, route and timing of vaccination, vaccine boosting, adjunctive therapies, and options for public health vaccination polices.
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Until the emergence of COVID-19, influenza had for many decades been the deadliest vaccine-preventable viral respiratory disease, one for which only less than suboptimal vaccines are available. Surprisingly, little has changed with influenza vaccines since 1957 when they were first administered in US national vaccination programs. Over the years, influenza vaccines have never been able to elicit durable protective immunity against seasonal influenza virus strains, even against non-drifted strains. Although current influenza vaccines reduce the risk of severe disease, hospitalization, and death to some degree, their effectiveness against clinically apparent infection is decidedly suboptimal, ranging from 14% to 60% over the past 15 influenza seasons. Furthermore, the duration of vaccine-elicited immunity is measured only in months. Current vaccines require annual re-vaccination with updated formulations that are frequently not precisely matched to circulating virus strains.8 Although annual influenza vaccinations are strongly recommended for most of the general public and especially for persons in high-risk groups, including the elderly, those with chronic diseases, and pregnant women, vaccine acceptance by the general public is not ideal.9
During the COVID-19 pandemic, the rapid development and deployment of SARS-CoV-2 vaccines has saved innumerable lives and helped to achieve early partial pandemic control. However, as variant SARS-CoV-2 strains have emerged, deficiencies in these vaccines reminiscent of influenza vaccines have become apparent. The vaccines for these two very different viruses have common characteristics: they elicit incomplete and short-lived protection against evolving virus variants that escape population immunity. Considering that vaccine development and licensure is a long and complex process requiring years of preclinical and clinical safety and efficacy data, the limitations of influenza and SARS-CoV-2 vaccines remind us that candidate vaccines for most other respiratory viruses have to date been insufficiently protective for consideration of licensure, including candidate vaccines against RSV, a major killer of infants and the elderly, parainfluenzaviruses, endemic coronaviruses,22 and many other “common cold” viruses that cause significant morbidity and economic loss.
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I'm a big fan that you're still getting boosters.
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You’re a fucking idiot.
Lockdowns did jack shit positively.
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Never had Covid, nor myocarditis for that matter.
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But what about your anal warts?
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His monkey pox must be itchy! Better get the vax Cuck. It's called NoFaggala.
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And?
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Your odds of not having "attained" the virus (shoutout to Magic) are actually quite low.
Although you do seem like the type who would test for covid if you had seasonal allergy sniffles, and you do seem like a basement dweller.
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Again, I don’t know how many times I need to school you guys in subjects before you realize I’ve done my homework while you dipshits shoot from the hip (see NVDA post below).
If you guys hate that vaccine so much, then shoot blame your leader Trump who invented it and pushed it out. Why does he get a free pass in your eyes?









