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10.1111/jcmm.15771

http://scihub22266oqcxt.onion/10.1111/jcmm.15771
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32975374!7537162!32975374
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suck abstract from ncbi


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pmid32975374      J+Cell+Mol+Med 2020 ; 24 (21): 12457-12463
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  • Naturally activated adaptive immunity in COVID-19 patients #MMPMID32975374
  • Yang X; Dai T; Zhou X; Qian H; Guo R; Lei L; Zhang X; Zhang D; Shi L; Cheng Y; Hu J; Guo Y; Zhang B
  • J Cell Mol Med 2020[Nov]; 24 (21): 12457-12463 PMID32975374show ga
  • Coronavirus disease-2019 (COVID-19) caused by severe acute respiratory syndrome coronavirus (SARS-CoV-2) has rapidly spread worldwide, threatening the health and lives of many people. Unfortunately, information regarding the immunological characteristics of COVID-19 patients remains limited. Herein, we collected blood samples from 18 healthy donors (HDs) and 38 COVID-19 patients to analyse changes in the adaptive immune cell populations and their phenotypes. We observed that the lymphocyte percentage moderately decreased, CD4 and CD8 T cell percentage among lymphocytes were similar, and B cell percentage was increased in COVID-19 patients in comparison to that in HDs. T cells, especially CD8 T cells, showed an enhanced expression of late activation marker CD25 and exhaustion marker PD-1. Importantly, SARS-CoV-2 infection increased the percentage of T follicular helper- and germinal centre B-like cells in the blood. The parameters in COVID-19 patients remained unchanged across various age groups. Therefore, we demonstrated that the T and B cells are activated naturally and are functional during SARS-CoV-2 infection. These data provide evidence that the adaptive immunity in most patients could be primed to induce a significant immune response against SARS-CoV-2 infection upon receiving standard medical care.
  • |*Adaptive Immunity[MESH]
  • |Adult[MESH]
  • |Antigens, CD/metabolism[MESH]
  • |B-Lymphocytes/virology[MESH]
  • |CD4-Positive T-Lymphocytes/immunology/virology[MESH]
  • |CD8-Positive T-Lymphocytes/immunology/virology[MESH]
  • |COVID-19/blood/*immunology[MESH]
  • |Female[MESH]
  • |Humans[MESH]
  • |Immunophenotyping[MESH]
  • |Male[MESH]
  • |Programmed Cell Death 1 Receptor/metabolism[MESH]


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