Author:
Niu Xuefeng,Li Song,Li Pingchao,Pan Wenjing,Wang Qian,Feng Ying,Mo Xiaoneng,Yan Qihong,Ye Xianmiao,Luo Jia,Qu Linbing,Weber Daniel,Byrne-Steele Miranda L.,Wang Zhe,Yu Fengjia,Li Fang,Myers Richard M.,Lotze Michael T.,Zhong Nanshan,Han Jian,Chen Ling
Abstract
Severe COVID-19 is associated with profound lymphopenia and an elevated neutrophil to lymphocyte ratio. We applied a novel dimer avoidance multiplexed polymerase chain reaction next-generation sequencing assay to analyze T (TCR) and B cell receptor (BCR) repertoires. Surprisingly, TCR repertoires were markedly diminished during the early onset of severe disease but recovered during the convalescent stage. Monitoring TCR repertoires could serve as an indicative biomarker to predict disease progression and recovery. Panoramic concurrent assessment of BCR repertoires demonstrated isotype switching and a transient but dramatic early IgA expansion. Dominant B cell clonal expansion with decreased diversity occurred following recovery from infection. Profound changes in T cell homeostasis raise critical questions about the early events in COVID-19 infection and demonstrate that immune repertoire analysis is a promising method for evaluating emergent host immunity to SARS-CoV-2 viral infection, with great implications for assessing vaccination and other immunological therapies.
Funder
National Natural Science Foundation of China-Yunnan Joint Fund
Subject
Immunology,Immunology and Allergy
Cited by
57 articles.
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