Immune response against the severe acute respiratory syndrome coronavirus 2

被引:3
|
作者
Ferenc, Uher [1 ]
Zsolt, Matula [1 ]
Marton, Gonczi [1 ]
Laszlo, Gopcsa [1 ]
Gabriella, Beko [1 ]
Marienn, Reti [1 ]
Zoltan, Szekanecz [2 ]
Eva, Ajzner [1 ]
Istvan, Valyi-Nagy [1 ]
机构
[1] Orszagos Hematol & Infektol Int, Del Pesti Cent korhaz, Budapest, Hungary
[2] Debreccni Egyet, Altalanos Orvostud Kar, Reumatol Tanszek, Debrecen, Hungary
关键词
adaptive immunity; antibodies; B and T cell memory; cytokines; innate immunity; interferon; INNATE IMMUNITY; T-CELLS; SARS-COV-2; MECHANISMS;
D O I
10.1556/650.2022.32521
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Coronavirus disease 2019 (COVID???19) displays tremendous inter-individual variability, ranging from asymptomatic infections to life-threatening illness. Although more studies are needed, a picture has begun to emerge that variability in the immune system components is a main contributor to the heterogeneous disease courses. Here, we provide a concept for the interaction of the innate and adaptive immune systems with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) to link the observations that have been made during the first two years of the pandemic. Inborn errors of, and autoantibodies directed against, type I interferons, dysregulated myeloid response, hyperinflammation, lymphopenia, lymphocyte impairment, and heterogeneous adaptive immunity to SARS-CoV-2 are discussed, as well as their impact in the course of COVID???19. In addition, we will also review part of the key findings that have helped define and delineate some of the essential attributes of SARS-CoV-2-specific humoral and cell -mediated immune memory.
引用
收藏
页码:774 / 787
页数:14
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