HCV感染合并门静脉高压症肝硬化患者脾CD4+和CD8+ t细胞高表达PD-1和Tim-3。

IF 3 3区 医学 Q3 IMMUNOLOGY
Na Huang, Rui Zhou, Haiyan Chen, Shu Zhang, Jun Li, Wei Wei, Jin Sun, Song Ren, Baohua Li, Hong Deng, Jun Yang, Fanpu Ji, Zongfang Li
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引用次数: 1

摘要

脾脏在调节机体对感染性病原体的免疫应答中起着重要作用。乙型/丙型肝炎病毒(HBV/HCV)感染患者中有t细胞功能障碍和衰竭的报道,这是导致持续病毒感染的原因。本研究的目的是探讨HCV肝硬化合并门脉高压(PH)患者免疫抑制和免疫耐受的脾相关证据。方法:采用实时荧光定量PCR和免疫组化技术,分析15例HCV肝硬化患者脾脏和肝脏中程序性细胞死亡1 (PD-1)、t细胞免疫球蛋白结构域和粘蛋白结构域含分子-3 (Tim-3)及其配体PD-L1/2、半乳糖凝集素-9的表达。采用流式细胞术检测PD-1、Tim-3在脾切除术前后脾脏及外周血t细胞上的表达情况(n = 8)。结果:PH患者脾脏中PD-L2、Tim-3、半凝集素-9、CD80、CD86 mRNA表达水平与对照组(创伤性脾切除)相比显著升高(p < 0.05), CD28 mRNA表达水平显著降低(p < 0.05)。肝硬化患者脾脏和肝脏抑制信号分子蛋白表达均显著高于对照组(p < 0.05)。肝硬化患者外周血和脾CD4+和CD8+ t细胞表达的PD-1、Tim-3和CTLA-4蛋白水平也高于健康对照组(均p < 0.05)。脾切除术后外周血PD-1+CD4+T淋巴细胞比例(26.2%±7.12%比21.0%±9.14%,p = 0.0293)和Tim-3+CD8+ T淋巴细胞比例(9.4%±3.04%比6.0%±2.24%,p = 0.0175)降低。结论:hcv感染和肝硬化门静脉高压症患者脾和外周血CD4+和CD8+ t细胞高表达PD-1和Tim-3。脾切除术后外周血t淋巴细胞高表达的PD-1和Tim-3可部分逆转。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Splenic CD4<sup>+</sup> and CD8<sup>+</sup> T-cells highly expressed PD-1 and Tim-3 in cirrhotic patients with HCV infection and portal hypertension.

Splenic CD4<sup>+</sup> and CD8<sup>+</sup> T-cells highly expressed PD-1 and Tim-3 in cirrhotic patients with HCV infection and portal hypertension.

Splenic CD4<sup>+</sup> and CD8<sup>+</sup> T-cells highly expressed PD-1 and Tim-3 in cirrhotic patients with HCV infection and portal hypertension.

Splenic CD4+ and CD8+ T-cells highly expressed PD-1 and Tim-3 in cirrhotic patients with HCV infection and portal hypertension.

Introduction: The spleen plays an important role in regulating the immune response to infectious pathogens. T-cells dysfunction and exhaustion have been reported in patients with hepatitis B/C virus (HBV/HCV) infection, which contributes to persistent virus infection. The aims of this study were to investigate spleen-related evidence of immunosuppression and immune tolerance in HCV cirrhotic patients with portal hypertension (PH). Methods: The expression of programmed cell death 1 (PD-1), T-cell immunoglobulin domain and mucin domain-containing molecule-3 (Tim-3) and its ligand PD-L1/2, and Galectin-9 in the spleens and livers of HCV cirrhotic patients (n = 15) was analyzed using real-time PCR and immunohistochemistry. Flow cytometry was used to evaluate the expression of PD-1 and Tim-3 on splenic T-cells and the peripheral blood T-cells before and after splenectomy (n = 8). Results: Spleens from patients with PH showed significantly increased mRNA levels of PD-L2, Tim-3, Galectin-9, CD80, and CD86, and decreased levels of CD28 compared to control spleens (spleens removed due to traumatic injury) (all p < 0.05). Additionally, protein expression of inhibitory signaling molecules was significantly increased in both the spleens and livers of cirrhotic patients compared with controls (all p < 0.05). Peripheral blood and splenic CD4+ and CD8+ T-cells also expressed higher protein levels of PD-1, Tim-3, and CTLA-4 in cirrhotic patients as compared with healthy controls (all p < 0.05). The proportion of PD-1+CD4+T lymphocytes (26.2% ± 7.12% vs. 21.0% ± 9.14%, p = 0.0293) and Tim-3+CD8+ T lymphocytes (9.4% ± 3.04% vs. 6.0% ± 2.24%, p = 0.0175) in peripheral blood decreased followed splenectomy. Conclusion: The CD4+ and CD8+ T-cells in spleen and peripheral blood highly expressed PD-1 and Tim-3 in HCV-infected and cirrhotic patients with portal hypertension. Highly expressed PD-1 and Tim-3 in peripheral blood T-lymphocytes can be partly reversed following splenectomy.

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来源期刊
CiteScore
4.00
自引率
0.00%
发文量
88
审稿时长
15 weeks
期刊介绍: International Journal of Immunopathology and Pharmacology is an Open Access peer-reviewed journal publishing original papers describing research in the fields of immunology, pathology and pharmacology. The intention is that the journal should reflect both the experimental and clinical aspects of immunology as well as advances in the understanding of the pathology and pharmacology of the immune system.
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