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10.1038/s41598-021-85202-9

http://scihub22266oqcxt.onion/10.1038/s41598-021-85202-9
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33723294!7960719!33723294
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suck abstract from ncbi


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pmid33723294      Sci+Rep 2021 ; 11 (1): 5934
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  • SARS-CoV-2-induced humoral immunity through B cell epitope analysis in COVID-19 infected individuals #MMPMID33723294
  • Yoshida S; Ono C; Hayashi H; Fukumoto S; Shiraishi S; Tomono K; Arase H; Matsuura Y; Nakagami H
  • Sci Rep 2021[Mar]; 11 (1): 5934 PMID33723294show ga
  • The aim of this study is to understand adaptive immunity to SARS-CoV-2 through the analysis of B cell epitope and neutralizing activity in coronavirus disease 2019 (COVID-19) patients. We obtained serum from forty-three COVID-19 patients from patients in the intensive care unit of Osaka University Hospital (n = 12) and in Osaka City Juso Hospital (n = 31). Most individuals revealed neutralizing activity against SARS-CoV-2 assessed by a pseudotype virus-neutralizing assay. The antibody production against the spike glycoprotein (S protein) or receptor-binding domain (RBD) of SARS-CoV-2 was elevated, with large individual differences, as assessed by ELISA. We observed the correlation between neutralizing antibody titer and IgG, but not IgM, antibody titer of COVID-19 patients. In the analysis of the predicted the linear B cell epitopes, hot spots in the N-terminal domain of the S protein were observed in the serum from patients in the intensive care unit of Osaka University Hospital. Overall, the analysis of antibody production and B cell epitopes of the S protein from patient serum may provide a novel target for the vaccine development against SARS-CoV-2.
  • |*Immunity, Humoral[MESH]
  • |Amino Acid Sequence[MESH]
  • |Antibodies, Neutralizing/blood/immunology[MESH]
  • |Antibodies, Viral/blood/immunology[MESH]
  • |COVID-19/*epidemiology/*immunology/virology[MESH]
  • |Enzyme-Linked Immunosorbent Assay[MESH]
  • |Epitopes, B-Lymphocyte/*immunology[MESH]
  • |Female[MESH]
  • |Host-Pathogen Interactions[MESH]
  • |Humans[MESH]
  • |Male[MESH]
  • |SARS-CoV-2/*immunology[MESH]


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