慢性乙型肝炎病毒感染患者外周血单个核细胞中共刺激分子B7-2和PD-L1的表达

Lingxia Fei, Shipin Wu, Hongtao Chen
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引用次数: 0

摘要

目的探讨外周血单核细胞中共刺激分子B7-2和共抑制分子PD-L1的表达在慢性乙型肝炎病毒感染免疫耐受机制中的作用。方法选取30例处于免疫反应期的HBV感染者和20例处于免疫耐受期的HBV感染者,同时选取20名健康志愿者作为对照。采用RT- PCR和real-time PCR方法检测慢性HBV感染患者外周血单个核细胞B7-2和PD-L1 mRNA的表达水平。结果B7-2在免疫反应性和免疫耐受患者中的表达明显低于对照组(P均<0.01);B7-2在免疫反应性患者中的表达明显低于免疫耐受患者(P <0.01)。免疫反应性患者和免疫耐受患者的PD-L1表达明显高于正常对照组(P all <0.01)。免疫反应性和免疫耐受患者的PD-L1/B7-2比值显著高于健康对照组(P均<0.01);免疫反应性患者的PD-L1/B7-2比值明显高于免疫耐受患者(P <0.01)。结论在慢性HBV感染中,共刺激和共抑制分子表达的变化暗示了对患者免疫反应的保护性调整,可能导致免疫耐受性增加和HBV持续感染。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Expression of co-stimulatory molecules B7-2 and PD-L1 on peripheral blood mononuclear cells in patients with chronic hepatitis B virus infection

Objective

To explore the roles of the expression of the co-stimulatory molecule, B7-2, and the co-inhibitory molecule, PD-L1, on peripheral blood mononuclear cells in the mechanism of immunotolerance in chronic hepatitis B virus infection.

Methods

Thirty HBV infected patients in the immunoreactive phase and 20 patients in the immunotolerant phase were enrolled in the study, while 20 healthy volunteers were used as controls. RT- PCR and real-time PCR methods were used to detect the expression levels of B7-2 and PD-L1 mRNA in peripheral blood mononuclear cells in chronic HBV infected patients.

Results

The B7-2 expression in immunoreactive and immunotolerant patients was significantly lower than that in the controls (P all < 0.01); B7-2 expression in immunoreactive patients was significantly lower than in immunotolerant patients (P < 0.01). PD-L1 expression in immunoreactive patients and immunotolerant patients was significantly higher than that in normal controls (P all < 0.01). The PD-L1/B7-2 ratios in immunoreactive and immunotolerant patients were significantly higher than that of the healthy controls (P all < 0.01); the PD-L1/B7-2 ratio was significantly higher in the immunoreactive patients than in the immunotolerant patients (P < 0.01).

Conclusion

In chronic HBV infection, changes in the expression of co-stimulatory and co-inhibitory molecules imply a protective adjustment against the patient's immune response that may result in increased immunotolerance and persistent HBV infection.

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