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Clin Infect Dis. 2020 Nov 19;71(16):2150-2157. doi: 10.1093/cid/ciaa630.
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胸腺素 α1 通过恢复淋巴细胞减少症和逆转耗竭 T 细胞来降低严重 COVID-19 的死亡率。

Thymosin Alpha 1 Reduces the Mortality of Severe Coronavirus Disease 2019 by Restoration of Lymphocytopenia and Reversion of Exhausted T Cells.

机构信息

Department of Medical Laboratory Center, General Hospital of the Central Theater Command, Wuhan, Hubei Province, People's Republic of China.

Institute of Immunology, People's Liberation Army, Third Military Medical University, Chongqing, People's Republic of China.

出版信息

Clin Infect Dis. 2020 Nov 19;71(16):2150-2157. doi: 10.1093/cid/ciaa630.

DOI:10.1093/cid/ciaa630
PMID:32442287
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7314217/
Abstract

BACKGROUND

Thymosin alpha 1 (Tα1) had been used in the treatment of viral infections as an immune response modifier for many years. However, clinical benefits and the mechanism of Tα1 treatment for COVID-19 patients are still unclear.

METHODS

We retrospectively reviewed the clinical outcomes of 76 severe COVID-19 cases admitted to 2 hospitals in Wuhan, China, from December 2019 to March 2020. The thymus output in peripheral blood mononuclear cells from COVID-19 patients was measured by T-cell receptor excision circles (TRECs). The levels of T-cell exhaustion markers programmed death-1 (PD-1) and T-cell immunoglobulin and mucin domain protein 3 (Tim-3) on CD8+ T cells were detected by flow cytometry.

RESULTS

Compared with the untreated group, Tα1 treatment significantly reduced the mortality of severe COVID-19 patients (11.11% vs 30.00%, P = .044). Tα1 enhanced blood T-cell numbers in COVID-19 patients with severe lymphocytopenia. Under such conditions, Tα1 also successfully restored CD8+ and CD4+ T-cell numbers in elderly patients. Meanwhile, Tα1 reduced PD-1 and Tim-3 expression on CD8+ T cells from severe COVID-19 patients compared with untreated cases. It is of note that restoration of lymphocytopenia and acute exhaustion of T cells were roughly parallel to the rise of TRECs.

CONCLUSIONS

Tα1 treatment significantly reduced mortality of severe COVID-19 patients. COVID-19 patients with counts of CD8+ T cells or CD4+ T cells in circulation less than 400/μL or 650/μL, respectively, gained more benefits from Tα1. Tα1 reversed T-cell exhaustion and recovered immune reconstitution through promoting thymus output during severe acute respiratory syndrome-coronavirus 2 infection.

摘要

背景

胸腺肽α1(Tα1)多年来一直被用作病毒感染的治疗药物,作为一种免疫反应调节剂。然而,Tα1 治疗 COVID-19 患者的临床获益和机制仍不清楚。

方法

我们回顾性分析了 2019 年 12 月至 2020 年 3 月期间中国武汉的 2 家医院收治的 76 例重症 COVID-19 患者的临床结局。通过 T 细胞受体切除环(TREC)测量 COVID-19 患者外周血单个核细胞中的胸腺输出。通过流式细胞术检测 CD8+T 细胞上程序性死亡-1(PD-1)和 T 细胞免疫球蛋白和粘蛋白结构域蛋白 3(Tim-3)的 T 细胞耗竭标志物水平。

结果

与未治疗组相比,Tα1 治疗显著降低了重症 COVID-19 患者的死亡率(11.11%比 30.00%,P=0.044)。Tα1 增强了 COVID-19 患者严重淋巴细胞减少症患者的血液 T 细胞数量。在这种情况下,Tα1 还成功恢复了老年患者的 CD8+和 CD4+T 细胞数量。同时,与未治疗组相比,Tα1 降低了严重 COVID-19 患者 CD8+T 细胞上 PD-1 和 Tim-3 的表达。值得注意的是,淋巴细胞减少症的恢复和 T 细胞的急性耗竭与 TRECs 的升高大致平行。

结论

Tα1 治疗显著降低了重症 COVID-19 患者的死亡率。循环中 CD8+T 细胞或 CD4+T 细胞计数分别低于 400/μL 或 650/μL 的 COVID-19 患者从 Tα1 中获益更多。Tα1 通过在严重急性呼吸综合征冠状病毒 2 感染期间促进胸腺输出,逆转了 T 细胞耗竭并恢复了免疫重建。