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10.1101/2021.07.28.453981

http://scihub22266oqcxt.onion/10.1101/2021.07.28.453981
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suck abstract from ncbi


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pmid34341788      bioRxiv 2021 ; ä (ä): ä
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  • Single-Cell Profiling of the Antigen-Specific Response to BNT162b2 SARS-CoV-2 RNA Vaccine #MMPMID34341788
  • Kramer KJ; Wilfong EM; Voss K; Barone SM; Shiakolas AR; Raju N; Roe CE; Suryadevara N; Walker L; Wall SC; Paulo A; Schaefer S; Dahunsi D; Westlake CS; Crowe JE; Carnahan RH; Rathmell JC; Bonami RH; Georgiev IS; Irish JM
  • bioRxiv 2021[Jul]; ä (ä): ä PMID34341788show ga
  • RNA-based vaccines against SARS-CoV-2 are critical to limiting COVID-19 severity and spread. Cellular mechanisms driving antigen-specific responses to these vaccines, however, remain uncertain. We used single-cell technologies to identify and characterized antigen-specific cells and antibody responses to the RNA vaccine BNT162b2 in longitudinal samples from a cohort of healthy donors. Mass cytometry and machine learning pinpointed a novel expanding, population of antigen-specific non-canonical memory CD4 (+) and CD8 (+) T cells. B cell sequencing suggested progression from IgM, with apparent cross-reactivity to endemic coronaviruses, to SARS-CoV-2-specific IgA and IgG memory B cells and plasmablasts. Responding lymphocyte populations correlated with eventual SARS-CoV-2 IgG and a donor lacking these cell populations failed to sustain SARS-CoV-2-specific antibodies and experienced breakthrough infection. These integrated proteomic and genomic platforms reveal an antigen-specific cellular basis of RNA vaccine-based immunity. ONE SENTENCE SUMMARY: Single-cell profiling reveals the cellular basis of the antigen-specific response to the BNT162b2 SARS-CoV-2 RNA vaccine.
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