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10.1016/j.vaccine.2021.10.074

http://scihub22266oqcxt.onion/10.1016/j.vaccine.2021.10.074
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34802792!8580836!34802792
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suck abstract from ncbi


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pmid34802792      Vaccine 2021 ; 39 (51): 7367-7374
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  • BNT162b2 mRNA COVID-19 vaccine Reactogenicity: The key role of immunity #MMPMID34802792
  • Vizcarra P; Haemmerle J; Velasco H; Velasco T; Fernandez-Escribano M; Vallejo A; Casado JL
  • Vaccine 2021[Dec]; 39 (51): 7367-7374 PMID34802792show ga
  • We examined the impact of pre-existing SARS-CoV-2-specific cellular immunity on BNT162b2 mRNA COVID-19 vaccine reactogenicity. Of 96 healthcare workers (HCWs), 76% reported any vaccine reaction (first dose: 70%, second dose: 67%), none of which was severe. Following first dose, systemic reactions were significantly more frequent among HCWs with past infection than in infection-naive individuals, and among HCWs with pre-existing cellular immunity than in those without it. The rate of systemic reactions after second dose was 1.7 and 2.0-times higher than after first dose among infection-naive HCWs and those without pre-existing cellular immunity, respectively. Levels of SARS-CoV-2-specific T-cells before vaccination were higher in HCWs with systemic reactions after the first dose than in those without them. BNT162b2 vaccine reactogenicity after first dose is attributable to pre-existing cellular immunity elicited by prior COVID-19 or cross-reactivity. Reactogenicity following second dose suggests an immunity-boosting effect. Overall, these data may reduce negative attitudes towards COVID-19 vaccines. Study Registration. The study was registered on clinicaltrials.gov, NCT04402827.
  • |*COVID-19[MESH]
  • |*COVID-19 Vaccines[MESH]
  • |BNT162 Vaccine[MESH]
  • |Humans[MESH]
  • |RNA, Messenger/genetics[MESH]


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