Literature DB >> 32324595

The laboratory tests and host immunity of COVID-19 patients with different severity of illness.

Feng Wang1, Hongyan Hou1, Ying Luo1, Guoxing Tang1, Shiji Wu1, Min Huang1, Weiyong Liu1, Yaowu Zhu1, Qun Lin1, Liyan Mao1, Minghao Fang2, Huilan Zhang3, Ziyong Sun1.   

Abstract

BACKGROUNDThe coronavirus disease 2019 (COVID-19), infected by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), has caused a severe outbreak throughout the world. The host immunity of COVID-19 patients is unknown.METHODSThe routine laboratory tests and host immunity in COVID-19 patients with different severity of illness were compared after patient admission.RESULTSA total of 65 SARS-CoV-2-positive patients were classified as having mild (n = 30), severe (n = 20), and extremely severe (n = 15) illness. Many routine laboratory tests, such as ferritin, lactate dehydrogenase, and D-dimer, were increased in severe and extremely severe patients. The absolute numbers of CD4+ T cells, CD8+ T cells, and B cells were gradually decreased with increased severity of illness. The activation markers such as HLA-DR and CD45RO expressed on CD4+ and CD8+ T cells were increased in severe and extremely severe patients compared with mild patients. The costimulatory molecule CD28 had opposite results. The percentage of natural Tregs was decreased in extremely severe patients. The percentage of IFN-γ-producing CD8+ T cells was increased in both severe and extremely severe patients compared with mild patients. The percentage of IFN-γ-producing CD4+ T cells was increased in extremely severe patients. IL-2R, IL-6, and IL-10 were all increased in extremely severe patients. The activation of DC and B cells was decreased in extremely severe patients.CONCLUSIONThe number and function of T cells are inconsistent in COVID-19 patients. The hyperfunction of CD4+ and CD8+ T cells is associated with the pathogenesis of extremely severe SARS-CoV-2 infection.FUNDINGThis work was funded by the National Mega Project on Major Infectious Disease Prevention (2017ZX10103005-007) and the Fundamental Research Funds for the Central Universities (2019kfyRCPY098).

Entities:  

Keywords:  Adaptive immunity; Cellular immune response; Immunology; Infectious disease; Innate immunity

Mesh:

Substances:

Year:  2020        PMID: 32324595      PMCID: PMC7259533          DOI: 10.1172/jci.insight.137799

Source DB:  PubMed          Journal:  JCI Insight        ISSN: 2379-3708


  24 in total

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