School of Cellular and Molecular Medicine, University of Bristol, Bristol, United Kingdom.
Academic Respiratory Unit, North Bristol NHS Trust, Bristol, United Kingdom.
Elife. 2023 Jun 13;12:e85009. doi: 10.7554/eLife.85009.
Coronavirus disease-19 (COVID-19) causes immune perturbations which may persist long term, and patients frequently report ongoing symptoms for months after recovery. We assessed immune activation at 3-12 months post hospital admission in 187 samples from 63 patients with mild, moderate, or severe disease and investigated whether it associates with long COVID. At 3 months, patients with severe disease displayed persistent activation of CD4 and CD8 T-cells, based on expression of HLA-DR, CD38, Ki67, and granzyme B, and elevated plasma levels of interleukin-4 (IL-4), IL-7, IL-17, and tumor necrosis factor-alpha (TNF-α) compared to mild and/or moderate patients. Plasma from severe patients at 3 months caused T-cells from healthy donors to upregulate IL-15Rα, suggesting that plasma factors in severe patients may increase T-cell responsiveness to IL-15-driven bystander activation. Patients with severe disease reported a higher number of long COVID symptoms which did not however correlate with cellular immune activation/pro-inflammatory cytokines after adjusting for age, sex, and disease severity. Our data suggests that long COVID and persistent immune activation may correlate independently with severe disease.
新型冠状病毒病-19(COVID-19)可导致免疫紊乱,这些紊乱可能长期存在,并且患者在康复后数月内经常报告持续存在症状。我们评估了 63 名轻症、中症或重症患者的 187 个样本在出院后 3-12 个月的免疫激活情况,并调查其是否与长新冠有关。3 个月时,与轻症和/或中症患者相比,重症患者的 CD4 和 CD8 T 细胞持续表达 HLA-DR、CD38、Ki67 和颗粒酶 B,以及细胞因子 IL-4、IL-7、IL-17 和肿瘤坏死因子-α(TNF-α)的水平升高,表明重症患者的血浆因子可能会增加 T 细胞对 IL-15 的反应性,从而导致旁观者激活。重症患者报告了更多的长新冠症状,但在调整年龄、性别和疾病严重程度后,这些症状与细胞免疫激活/促炎细胞因子并无相关性。我们的数据表明,长新冠和持续的免疫激活可能与重症独立相关。