IFN-γ decreases PD-1 in T lymphocytes from convalescent COVID-19 patients via the AKT/GSK3β signaling pathway

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作者
Meijuan Song
Xiangqun Liu
Weiyu Shen
Zhengxia Wang
Jingjing Wu
Jingxian Jiang
Yanan Liu
Tingting Xu
Tao Bian
Mingshun Zhang
Wei Sun
Mao Huang
Ningfei Ji
机构
[1] Jiangsu Province People’s Hospital and Nanjing Medical University First Affiliated Hospital,Department of Respiratory and Critical Care Medicine
[2] The Xuzhou Municipal Hospital Affiliated to Xuzhou Medical University,Department of Respiratory and Critical Care Medicine
[3] Wuxi People’s Hospital Affiliated to Nanjing Medical University,Department of Respiratory and Critical Care Medicine
[4] Nanjing Medical University,Jiangsu Province Engineering Research Center of Antibody Drug, NHC Key Laboratory of Antibody Technique, Department of Immunology
[5] Xishan People’s Hospital of Wuxi City,Department of Respiratory and Critical Care Medicine
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Coronavirus disease 2019; Convalescent patients; CD8; T cells; PD-1; IFN-γ;
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摘要
Post-COVID-19 syndrome may be associated with the abnormal immune status. Compared with the unexposed age-matched elder group, PD-1 in the CD8+ T cells from recovered COVID-19 patients was significantly lower. IFN-γ in the plasma of COVID-19 convalescent patients was increased, which inhibited PD-1 expression in CD8+ T cells from COVID-19 convalescent patients. scRNA-seq bioinformatics analysis revealed that AKT/GSK3β may regulate the INF-γ/PD-1 axis in CD8+ T cells from COVID-19 convalescent patients. In parallel, an IFN-γ neutralizing antibody reduced AKT and increased GSK3β in PBMCs. An AKT agonist (SC79) significantly decreased p-GSK3β. Moreover, AKT decreased PD-1 on CD8+ T cells, and GSK3β increased PD-1 on CD8+ T cells according to flow cytometry analysis. Collectively, we demonstrated that recovered COVID-19 patients may develop long COVID. Increased IFN-γ in the plasma of recovered Wuhan COVID-19 patients contributed to PD-1 downregulation on CD8+ T cells by regulating the AKT/GSK3β signaling pathway.
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