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10.1038/s41423-021-00750-4

http://scihub22266oqcxt.onion/10.1038/s41423-021-00750-4
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34413488!8374113!34413488
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suck abstract from ncbi


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pmid34413488      Cell+Mol+Immunol 2021 ; 18 (10): 2325-2333
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  • Activation or exhaustion of CD8(+) T cells in patients with COVID-19 #MMPMID34413488
  • Rha MS; Shin EC
  • Cell Mol Immunol 2021[Oct]; 18 (10): 2325-2333 PMID34413488show ga
  • In addition to CD4(+) T cells and neutralizing antibodies, CD8(+) T cells contribute to protective immune responses against SARS-CoV-2 in patients with coronavirus disease 2019 (COVID-19), an ongoing pandemic disease. In patients with COVID-19, CD8(+) T cells exhibiting activated phenotypes are commonly observed, although the absolute number of CD8(+) T cells is decreased. In addition, several studies have reported an upregulation of inhibitory immune checkpoint receptors, such as PD-1, and the expression of exhaustion-associated gene signatures in CD8(+) T cells from patients with COVID-19. However, whether CD8(+) T cells are truly exhausted during COVID-19 has been a controversial issue. In the present review, we summarize the current understanding of CD8(+) T-cell exhaustion and describe the available knowledge on the phenotypes and functions of CD8(+) T cells in the context of activation and exhaustion. We also summarize recent reports regarding phenotypical and functional analyses of SARS-CoV-2-specific CD8(+) T cells and discuss long-term SARS-CoV-2-specific CD8(+) T-cell memory.
  • |CD8-Positive T-Lymphocytes/*immunology[MESH]
  • |COVID-19 Vaccines/immunology[MESH]
  • |COVID-19/*immunology[MESH]
  • |Humans[MESH]
  • |Immunologic Memory[MESH]
  • |Lymphocyte Activation[MESH]


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