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病例报告:干扰素-γ 恢复重症 COVID-19 伴获得性免疫抑制综合征中的单核细胞人类白细胞抗原受体 (mHLA-DR)。

Case Report: Interferon-γ Restores Monocytic Human Leukocyte Antigen Receptor (mHLA-DR) in Severe COVID-19 With Acquired Immunosuppression Syndrome.

机构信息

Department of Anesthesiology and Intensive Care Medicine, University Medical, Center Goettingen, Goettingen, Germany.

Department of Dermatology, University Medical Center Goettingen, Goettingen, Germany.

出版信息

Front Immunol. 2021 Apr 7;12:645124. doi: 10.3389/fimmu.2021.645124. eCollection 2021.

Abstract

BACKGROUND

The major histocompatibility complex (MHC) class II characterized by monocytes CD14+ expression of human leukocyte antigen receptors (HLA-DR), is essential for the synapse between innate and adaptive immune response in infectious disease. Its reduced expression is associated with a high risk of secondary infections in septic patients and can be safely corrected by Interferon-y (IFNy) injection. Coronavirus disease (COVID-19) induces an alteration of Interferon (IFN) genes expression potentially responsible for the observed low HLA-DR expression in circulating monocytes (mHLA-DR).

METHODS

We report a case of one-time INFy injection (100 mcg s.c.) in a superinfected 61-year-old man with COVID-19-associated acute respiratory distress syndrome (ARDS), with monitoring of mHLA-DR expression and clinical tolerance.

OBSERVATIONS

Low mHLA-DR pretreatment expression (26.7%) was observed. IFNy therapy leading to a rapid increase in mHLA-DR expression (83.1%).

CONCLUSIONS

Severe ARDS in a COVID-19 patient has a deep reduction in mHLA-DR expression concomitantly with secondary infections. The unique IFNy injection was safe and led to a sharp increase in the expression of mHLA-DR. Based on immune and infection monitoring, more cases of severe COVID-19 patients with low mHLA-DR should be treated by IFNy to test the clinical effectiveness.

摘要

背景

主要组织相容性复合体(MHC)Ⅱ类以人白细胞抗原受体(HLA-DR)在单核细胞 CD14+上的表达为特征,对于传染病中固有和适应性免疫反应之间的突触形成至关重要。其表达减少与脓毒症患者继发感染的风险增加相关,并可通过干扰素-y(IFNy)注射安全纠正。冠状病毒病(COVID-19)诱导干扰素(IFN)基因表达的改变,可能导致循环单核细胞中观察到的 HLA-DR 表达降低(mHLA-DR)。

方法

我们报告了一例 COVID-19 相关急性呼吸窘迫综合征(ARDS)合并继发感染的 61 岁男性单次注射 IFNy(100 mcg sc)的情况,监测 mHLA-DR 表达和临床耐受性。

观察结果

预处理时 mHLA-DR 表达较低(26.7%)。IFNy 治疗导致 mHLA-DR 表达迅速增加(83.1%)。

结论

COVID-19 患者的严重 ARDS 伴有 mHLA-DR 的深度降低,同时伴有继发感染。独特的 IFNy 注射是安全的,并导致 mHLA-DR 的表达急剧增加。基于免疫和感染监测,应更多地对 mHLA-DR 水平较低的严重 COVID-19 患者进行 IFNy 治疗,以检验其临床疗效。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/da09/8058468/615d44f80a9f/fimmu-12-645124-g001.jpg

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