Telomeres and COVID-19

被引:54
作者
Aviv, Abraham [1 ]
机构
[1] Rutgers State Univ, New Jersey Med Sch, Ctr Human Dev & Aging, Newark, NJ USA
关键词
COVID-19; lymphopenia; Telomeres; T cells; T-CELL; LENGTH; EXPRESSION; PNEUMONIA; IMMUNITY; CANCER; SPAN; SARS;
D O I
10.1096/fj.202001025
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The medical, public health, and scientific communities are grappling with monumental imperatives to contain COVID-19, develop effective vaccines, identify efficacious treatments for the infection and its complications, and find biomarkers that detect patients at risk of severe disease. The focus of this communication is on a potential biomarker, short telomere length (TL), that might serve to identify patients more likely to die from the SARS-CoV-2 infection, regardless of age. The common thread linking these patients is lymphopenia, which largely reflects a decline in the numbers of CD4/CD8 T cells but not B cells. These findings are consistent with data that lymphocyte TL dynamics impose a limit on T-cell proliferation. They suggest that T-cell lymphopoiesis might stall in individuals with short TL who are infected with SARS-CoV-2.
引用
收藏
页码:7247 / 7252
页数:6
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