Heterologous Immune Responses of Serum IgG and Secretory IgA Against the Spike Protein of Endemic Coronaviruses During Severe COVID-19

被引:9
|
作者
Smit, Wouter L. [1 ,2 ]
van Tol, Sophie [3 ]
van der Wal, Sanne [1 ]
van Vulpen, Femke [1 ]
la Grouw, Shannon [1 ]
van Lelyveld, Lenneke [4 ]
Limonard, Gijs [5 ]
Bossink, Ailko [5 ]
Godeke, Gert-Jan [3 ]
Shrestha, Sandhya [3 ]
Reimerink, Johan [3 ]
Eggink, Dirk [3 ]
Reusken, Chantal [3 ]
Heron, Michiel [1 ]
Thijsen, Steven [1 ]
机构
[1] Diakonessenhuis Utrecht, Dept Med Microbiol & Immunol, Utrecht, Netherlands
[2] Univ Med Ctr Utrecht, Dept Med Microbiol, Utrecht, Netherlands
[3] Natl Inst Publ Hlth & Environm RIVM, Ctr Infect Dis Control, Bilthoven, Netherlands
[4] Diakonessenhuis Utrecht, Dept Intens Care, Utrecht, Netherlands
[5] Diakonessenhuis Utrecht, Dept Pulm Dis, Utrecht, Netherlands
来源
FRONTIERS IN IMMUNOLOGY | 2022年 / 13卷
关键词
SARS-CoV-2; COVID-19; spike protein; seasonal coronaviruses; immune imprinting; SARS-COV-2;
D O I
10.3389/fimmu.2022.839367
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Defining immune correlates of disease severity is important to better understand the immunopathogenesis in COVID-19. Here we made use of a protein microarray platform to detect IgG- and IgA-reactive antibodies in sera and saliva respectively, and assess cross-reactivity between SARS-CoV-2 and endemic coronaviruses (eCoVs). IgG responses against the full protein of spike, but not the S1 subunit, were significantly higher in convalescent sera of patients with severe disease compared to mild disease and healthy controls. In addition, we detected reactivity of secretory IgA to eCoVs in saliva of patients with severe disease, not present in patients with moderate disease or seropositive healthy controls. These heterologous immune responses are in line with non-protective cross-reactivity, and support a potential role for immune imprinting in the pathogenesis of severe COVID-19.
引用
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页数:10
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