Department of Internal Medicine, Bærum Hospital, Vestre Viken Hospital Trust, Gjettum, Norway.
Division of Laboratory Medicine, Department of Immunology, Oslo University Hospital, Oslo, Norway.
J Infect Dis. 2022 Dec 13;226(12):2150-2160. doi: 10.1093/infdis/jiac313.
Immune dysregulation is a major factor in the development of severe coronavirus disease 2019 (COVID-19). The homeostatic chemokines CCL19 and CCL21 have been implicated as mediators of tissue inflammation, but data on their regulation in severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection is limited. We thus investigated the levels of these chemokines in COVID-19 patients.
Serial blood samples were obtained from patients hospitalized with COVID-19 (n = 414). Circulating CCL19 and CCL21 levels during hospitalization and 3-month follow-up were analyzed. In vitro assays and analysis of RNAseq data from public repositories were performed to further explore possible regulatory mechanisms.
A consistent increase in circulating levels of CCL19 and CCL21 was observed, with high levels correlating with disease severity measures, including respiratory failure, need for intensive care, and 60-day all-cause mortality. High levels of CCL21 at admission were associated with persisting impairment of pulmonary function at the 3-month follow-up.
Our findings highlight CCL19 and CCL21 as markers of immune dysregulation in COVID-19. This may reflect aberrant regulation triggered by tissue inflammation, as observed in other chronic inflammatory and autoimmune conditions. Determination of the source and regulation of these chemokines and their effects on lung tissue is warranted to further clarify their role in COVID-19.
NCT04321616 and NCT04381819.
免疫失调是导致严重 2019 冠状病毒病(COVID-19)的一个主要因素。稳态趋化因子 CCL19 和 CCL21 被认为是组织炎症的介质,但关于它们在严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)感染中的调节作用的数据有限。因此,我们研究了这些趋化因子在 COVID-19 患者中的水平。
从因 COVID-19 住院的患者中获得了一系列血液样本(n = 414)。分析了住院期间和 3 个月随访时的循环 CCL19 和 CCL21 水平。进行了体外测定和公共存储库的 RNAseq 数据分析,以进一步探索可能的调节机制。
观察到循环 CCL19 和 CCL21 水平持续升高,高水平与疾病严重程度的测量指标相关,包括呼吸衰竭、需要重症监护和 60 天全因死亡率。入院时高水平的 CCL21 与 3 个月随访时肺功能持续受损相关。
我们的研究结果强调了 CCL19 和 CCL21 作为 COVID-19 免疫失调的标志物。这可能反映了组织炎症引起的异常调节,如在其他慢性炎症和自身免疫性疾病中观察到的那样。确定这些趋化因子的来源和调节及其对肺组织的影响,对于进一步阐明它们在 COVID-19 中的作用是必要的。
NCT04321616 和 NCT04381819。