Impact of serum IL-10 level on the clinical outcome of COVID-19 patients and the development of post-COVID pulmonary fibrosis.

Mariam M Amin, Aliaa S Sheha, Mahetab Moustafa, Eman N Osman, Hossam M Elkady
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Abstract

A characteristic feature of the cytokine storm in coronavirus disease 2019 (COVID-19) is the dramatic elevation of serum interleukin 10 (IL-10). This may be a negative feedback mechanism to suppress inflammation. However, this IL-10 elevation may contribute to COVID-19 severity. In our study, we aimed to evaluate the effect of serum IL-10 level on patients' clinical outcome and the incidence of post-COVID19 pulmonary fibrosis. This was a prospective observational study, included 100 patients, confirmed to have COVID-19, Of these, 50 patients had COVID-19 without evidence of pneumonia in computed tomography (CT) scans (group I) and the other 50 patients had COVID-19 pneumonia (group II). Our results showed a significant increase in serum ferritin level in patients with COVID pneumonia. However, no difference was found in serum C-reactive protein (CRP) nor D-Dimer between both groups. There was a statistically significant increase in serum IL-10 in patients with COVID pneumonia compared with COVID patients without pneumonia (p < 0.001). Fibrosis was developed in 35 patients (70%) with COVID pneumonia after 3 months and 4 of them died, however, all patients without pneumonia survived. Among age, serum IL-10, aspartate aminotransferase (AST), alanine transaminase (ALT), elevated serum IL-10 was found to be an independent predictor of pneumonia (p=0.32). However, there was no significant effect for IL-10 on patients' clinical outcome. There was a statistically significant correlation between serum IL-10 levels and oxygen (O2) demand, CRP and D-Dimer (p= 0.015, p=0.034 and p=0.042, respectively). The higher the level of IL-10 the less fibrosis detected in follow up CT scans (p=0.038). In conclusion, even though IL-10 was significantly associated with disease severity (higher in pneumonia), elevated serum Il-10 has an independent role in decreasing the incidence of post-COVID-19 pulmonary fibrosis.

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血清 IL-10 水平对 COVID-19 患者临床结局和 COVID 后肺纤维化发展的影响。
冠状病毒病 2019(COVID-19)细胞因子风暴的一个特征是血清白细胞介素 10(IL-10)急剧升高。这可能是一种抑制炎症的负反馈机制。然而,IL-10的升高可能会导致COVID-19的严重程度。在我们的研究中,我们旨在评估血清 IL-10 水平对患者临床预后和 COVID-19 后肺纤维化发生率的影响。这是一项前瞻性观察研究,共纳入了 100 名确诊为 COVID-19 的患者,其中 50 名患者为 COVID-19 且在计算机断层扫描(CT)中无肺炎证据(I 组),另外 50 名患者为 COVID-19 肺炎(II 组)。结果显示,COVID-19 肺炎患者的血清铁蛋白水平明显升高。不过,两组患者的血清 C 反应蛋白(CRP)和 D-二聚体含量没有差异。与未患 COVID 肺炎的患者相比,COVID 肺炎患者的血清 IL-10 有明显增加(P < 0.001)。35 名 COVID 肺炎患者(70%)在 3 个月后出现纤维化,其中 4 人死亡,但所有未患肺炎的患者均存活。在年龄、血清 IL-10、天冬氨酸氨基转移酶(AST)、丙氨酸转氨酶(ALT)中,血清 IL-10 升高是肺炎的独立预测因子(P=0.32)。然而,IL-10 对患者的临床结果没有明显影响。血清 IL-10 水平与氧气(O2)需求量、CRP 和 D-Dimer 之间存在统计学意义上的显著相关性(分别为 p=0.015、p=0.034 和 p=0.042)。IL-10 水平越高,随访 CT 扫描发现的纤维化越少(p=0.038)。总之,尽管IL-10与疾病严重程度显著相关(肺炎患者的IL-10水平更高),但血清Il-10的升高在降低COVID-19后肺纤维化的发生率方面具有独立作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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