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10.1016/j.celrep.2021.109391

http://scihub22266oqcxt.onion/10.1016/j.celrep.2021.109391
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suck abstract from ncbi


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pmid34242574      Cell+Rep 2021 ; 36 (2): 109391
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  • Antibody landscape against SARS-CoV-2 reveals significant differences between non-structural/accessory and structural proteins #MMPMID34242574
  • Li Y; Xu Z; Lei Q; Lai DY; Hou H; Jiang HW; Zheng YX; Wang XN; Wu J; Ma ML; Zhang B; Chen H; Yu C; Xue JB; Zhang HN; Qi H; Guo SJ; Zhang Y; Lin X; Yao Z; Sheng H; Sun Z; Wang F; Fan X; Tao SC
  • Cell Rep 2021[Jul]; 36 (2): 109391 PMID34242574show ga
  • The immunogenicity of the SARS-CoV-2 proteome is largely unknown, especially for non-structural proteins and accessory proteins. In this study, we collect 2,360 COVID-19 sera and 601 control sera. We analyze these sera on a protein microarray with 20 proteins of SARS-CoV-2, building an antibody response landscape for immunoglobulin (Ig)G and IgM. Non-structural proteins and accessory proteins NSP1, NSP7, NSP8, RdRp, ORF3b, and ORF9b elicit prevalent IgG responses. The IgG patterns and dynamics of non-structural/accessory proteins are different from those of the S and N proteins. The IgG responses against these six proteins are associated with disease severity and clinical outcome, and they decline sharply about 20 days after symptom onset. In non-survivors, a sharp decrease of IgG antibodies against S1 and N proteins before death is observed. The global antibody responses to non-structural/accessory proteins revealed here may facilitate a deeper understanding of SARS-CoV-2 immunology.
  • |Adult[MESH]
  • |Aged[MESH]
  • |Antibodies, Viral/immunology[MESH]
  • |Antibody Formation[MESH]
  • |COVID-19/*immunology[MESH]
  • |Humans[MESH]
  • |Immunoglobulin G/immunology[MESH]
  • |Immunoglobulin M/immunology[MESH]
  • |Male[MESH]
  • |Middle Aged[MESH]
  • |Protein Array Analysis[MESH]
  • |SARS-CoV-2/*immunology[MESH]
  • |Spike Glycoprotein, Coronavirus/*immunology[MESH]
  • |Viral Nonstructural Proteins/*immunology[MESH]


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