Zhang Sifan, Asquith Becca, Szydlo Richard, Tregoning John S, Pollock Katrina M
Department of Infectious Disease, Imperial College London, London, UK.
Centre for Haematology, Department of Immunology and Inflammation, Imperial College London, London, UK.
Immunother Adv. 2021 Jul 2;1(1):ltab015. doi: 10.1093/immadv/ltab015. eCollection 2021 Jan.
Immunopathogenesis involving T lymphocytes, which play a key role in defence against viral infection, could contribute to the spectrum of COVID-19 disease and provide an avenue for treatment. To address this question, a review of clinical observational studies and autopsy data in English and Chinese languages was conducted with a search of registered clinical trials. Peripheral lymphopenia affecting CD4 and CD8 T cells was a striking feature of severe COVID-19 compared with non-severe disease. Autopsy data demonstrated infiltration of T cells into organs, particularly the lung. Seventy-four clinical trials are on-going that could target T cell-related pathogenesis, particularly IL-6 pathways. SARS-CoV-2 infection interrupts T cell circulation in patients with severe COVID-19. This could be due to redistribution of T cells into infected organs, activation induced exhaustion, apoptosis, or pyroptosis. Measuring T cell dynamics during COVID-19 will inform clinical risk-stratification of hospitalised patients and could identify those who would benefit most from treatments that target T cells.
涉及T淋巴细胞的免疫发病机制在抵御病毒感染中起关键作用,可能导致新冠病毒疾病的一系列症状,并为治疗提供途径。为解决这一问题,我们检索了注册临床试验,对中英文的临床观察性研究和尸检数据进行了综述。与非重症疾病相比,外周血淋巴细胞减少影响CD4和CD8 T细胞是重症新冠病毒疾病的一个显著特征。尸检数据显示T细胞浸润到器官中,尤其是肺。目前有74项正在进行的临床试验,其靶点可能是与T细胞相关的发病机制,特别是白细胞介素-6通路。严重新冠病毒疾病患者中,新冠病毒感染会中断T细胞循环。这可能是由于T细胞重新分布到受感染器官、激活诱导的耗竭、凋亡或细胞焦亡。在新冠病毒疾病期间测量T细胞动态将有助于对住院患者进行临床风险分层,并可识别出那些将从针对T细胞的治疗中获益最大的患者。