Department of Emergency Medicine.
Division of Critical Care Medicine, Department of Pediatrics; and.
J Clin Invest. 2021 Jan 4;131(1). doi: 10.1172/JCI143928.
Ongoing observational clinical research has prioritized understanding the human immune response to SARS-CoV-2 during the coronavirus disease 2019 (COVID-19) pandemic. Several recent studies suggest that immune dysregulation with early and prolonged adaptive immune system activation can result in cellular exhaustion. In this issue of the JCI, Files et al. compared cellular immune phenotypes during the first two months of COVID-19 in hospitalized and less severe, non-hospitalized patients. The authors utilized flow cytometry to analyze circulating peripheral blood mononuclear cells. Both patient cohorts maintained B and T cell phenotypes consistent with activation and cellular exhaustion throughout the first two months of infection. Additionally, follow-up samples from the non-hospitalized patient cohort showed that activation markers and cellular exhaustion increased over time. These findings illustrate the persistent nature of the adaptive immune system changes that have been noted in COVID-19 and suggest longer term effects that may shape the maintenance of immunity to SARS-CoV-2.
正在进行的观察性临床研究优先了解在 2019 年冠状病毒病(COVID-19)大流行期间人类对 SARS-CoV-2 的免疫反应。最近的几项研究表明,早期和持续的适应性免疫系统激活导致免疫失调,可导致细胞耗竭。在本期 JCI 中,Files 等人比较了住院和症状较轻、非住院患者在 COVID-19 发病的头两个月中的细胞免疫表型。作者利用流式细胞术分析了循环外周血单核细胞。在感染的头两个月中,两个患者队列均保持了与激活和细胞耗竭一致的 B 和 T 细胞表型。此外,非住院患者队列的随访样本显示,激活标志物和细胞耗竭随时间增加。这些发现说明了在 COVID-19 中观察到的适应性免疫系统变化的持续性质,并表明可能影响对 SARS-CoV-2 维持免疫的长期影响。