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10.4049/jimmunol.2100135

http://scihub22266oqcxt.onion/10.4049/jimmunol.2100135
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34049971!8627528!34049971
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suck abstract from ncbi


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pmid34049971      J+Immunol 2021 ; 206 (12): 2785-2790
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  • Cutting Edge: Distinct B Cell Repertoires Characterize Patients with Mild and Severe COVID-19 #MMPMID34049971
  • Hoehn KB; Ramanathan P; Unterman A; Sumida TS; Asashima H; Hafler DA; Kaminski N; Dela Cruz CS; Sealfon SC; Bukreyev A; Kleinstein SH
  • J Immunol 2021[Jun]; 206 (12): 2785-2790 PMID34049971show ga
  • Protective immunity against COVID-19 likely depends on the production of SARS-CoV-2-specific plasma cells and memory B cells postinfection or postvaccination. Previous work has found that germinal center reactions are disrupted in severe COVID-19. This may adversely affect long-term immunity against reinfection. Consistent with an extrafollicular B cell response, patients with severe COVID-19 have elevated frequencies of clonally expanded, class-switched, unmutated plasmablasts. However, it is unclear whether B cell populations in individuals with mild COVID-19 are similarly skewed. In this study, we use single-cell RNA sequencing of B cells to show that in contrast to patients with severe COVID-19, subjects with mildly symptomatic COVID-19 have B cell repertoires enriched for clonally diverse, somatically hypermutated memory B cells approximately 30 d after the onset of symptoms. This provides evidence that B cell responses are less disrupted in mild COVID-19 and result in the production of memory B cells.
  • |B-Lymphocytes/*immunology[MESH]
  • |COVID-19/*immunology[MESH]
  • |Cohort Studies[MESH]
  • |Humans[MESH]


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