Age-related susceptibility to coronavirus infections: role of impaired and dysregulated host immunity

被引:60
作者
Channappanavar, Rudragouda [1 ,2 ]
Perlman, Stanley [3 ,4 ]
机构
[1] Univ Tennessee, Hlth Sci Ctr, Dept Acute & Tertiary Care, Memphis, TN USA
[2] Univ Tennessee, Hlth Sci Ctr, Dept Microbiol Immunol & Biochem, Memphis, TN USA
[3] Univ Iowa, Roy J & Lucille A Carver Coll Med, Dept Microbiol & Immunol, Iowa City, IA USA
[4] Univ Iowa, Roy J & Lucille A Carver Coll Med, Stead Family Dept Pediat, Iowa City, IA USA
关键词
RESPIRATORY-SYNDROME CORONAVIRUS; T-CELL RESPONSES; SARS-CORONAVIRUS; DENDRITIC CELLS; MOUSE MODEL; CLINICAL CHARACTERISTICS; ANTIBODY-RESPONSES; UP-REGULATION; SOUTH-KOREA; IN-VITRO;
D O I
10.1172/JCI144115
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Human coronaviruses (hCoVs) cause severe respiratory illness in the elderly. Age-related impairments in innate immunity and suboptimal virus-specific T cell and antibody responses are believed to cause severe disease upon respiratory virus infections. This phenomenon has recently received increased attention, as elderly patients are at substantially elevated risk for severe COVID-19 disease and experience increased rates of mortality following SARS-CoV-2 infection compared with younger populations. However, the basis for age-related fatal pneumonia following pathogenic hCoVs is not well understood. In this Review, we provide an overview of our current understanding of hCoV-induced fatal pneumonia in the elderly. We describe host immune response to hCoV infections derived from studies of young and aged animal models and discuss the potential role of age-associated increases in sterile inflammation (inflammaging) and virus-induced dysregulated inflammation in causing age-related severe disease. We also highlight the existing gaps in our knowledge about virus replication and host immune responses to hCoV infection in young and aged individuals.
引用
收藏
页码:6204 / 6213
页数:10
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