T Lymphocyte Subset Counts and Interferon-Gamma Production in Adults and Children with COVID-19: A Narrative Review

被引:5
作者
De Rose, Domenico Umberto [1 ,2 ]
Pace, Pier Giorgio [3 ]
Ceccherini-Silberstein, Francesca [4 ]
Dotta, Andrea [1 ]
Andreoni, Massimo [3 ]
Sarmati, Loredana [3 ]
Iannetta, Marco [3 ]
机构
[1] Bambino Gesu Childrens Hosp IRCCS, Neonatal Intens Care Unit, I-00165 Rome, Italy
[2] Tor Vergata Univ Rome, Fac Med & Surg, Microbiol Immunol Infect Dis & Transplants MIMIT, I-00133 Rome, Italy
[3] Tor Vergata Univ & Hosp, Dept Syst Med, Infect Dis Unit, I-00133 Rome, Italy
[4] Tor Vergata Univ & Hosp, Dept Expt Med, I-00133 Rome, Italy
关键词
SARS-CoV-2; COVID-19; outcome; T cell exhaustion; cytokine storm; inflammation; respiratory outcome; CD3; IFN; IGRA; QuantiFERON-TB Gold; lymphopenia; MULTISYSTEM INFLAMMATORY SYNDROME; SUSCEPTIBILITY; LYMPHOPENIA; CELLS;
D O I
10.3390/jpm13050755
中图分类号
R19 [保健组织与事业(卫生事业管理)];
学科分类号
摘要
Adults and children exhibit a broad range of clinical outcomes from SARS-CoV-2 infection, with minimal to mild symptoms, especially in the pediatric age. However, some children present with a severe hyperinflammatory post-infectious complication named multisystem inflammatory syndrome in children (MIS-C), mainly affecting previously healthy subjects. Understanding these differences is still an ongoing challenge, that can lead to new therapeutic strategies and avoid unfavorable outcomes. In this review, we discuss the different roles of T lymphocyte subsets and interferon-? (IFN-?) in the immune responses of adults and children. Lymphopenia can influence these responses and represent a good predictor for the outcome, as reported by most authors. The increased IFN-? response exhibited by children could be the starting point for the activation of a broad response that leads to MIS-C, with a significantly higher risk than in adults, although a single IFN signature has not been identified. Multicenter studies with large cohorts in both age groups are still needed to study SARS-CoV-2 pathogenesis with new tools and to understand how is possible to better modulate immune responses.
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页数:14
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