首页|慢性乙型肝炎病毒感染患者CD8+T细胞中LAG-3的表达特征及临床意义

慢性乙型肝炎病毒感染患者CD8+T细胞中LAG-3的表达特征及临床意义

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[目的]探讨慢性乙型肝炎病毒(HBV)感染患者 CD8+T细胞中淋巴细胞活化基因-3(LAG-3)的表达特征及临床意义.[方法]选取 2019 年 4 月至 2020 年 4 月本院收治的 60 例慢性HBV患者(HBV组),另外选取同期于本院体检的 60 例健康志愿者作为对照组.比较两组 CD8+ T 细胞中 LAG-3 表达水平、表达强度、分布频数,并测定细胞内白介素-10(IL-10)、人类白细胞抗原-DR(HLA-DR)、干扰素-γ(IFN-γ)、转录因子 T-bet(T-bet)表达水平,分析 LAG-3 调控CD8+T细胞的机制.[结果]HBV组 LAG-3 的表达水平、表达强度高于对照组(P<0.05).HBV组 LAG-3 阳性亚群的 IL-10 表达水平高于阴性亚群,且 HBV组 LAG-3 阴性亚群、阳性亚群的 IL-10 表达水平均高于对照组(P<0.05).HBV组LAG-3 阳性亚群的 HLA-DR表达水平低于阴性亚群,且 HBV组LAG-3 阴性亚群、阳性亚群的 HLA-DR表达水平均低于对照组(P<0.05).HBV组LAG-3 阳性亚群的IFN-γ表达水平低于阴性亚群,且 HBV组 LAG-3 阴性亚群、阳性亚群 IFN-γ表达水平低于对照组(P<0.05).HBV 组 LAG-3 阳性亚群的T-bet表达水平低于阴性亚群,且 HBV组阴性亚群、阳性亚群 IFN-γ表达水平低于对照组(P<0.05).[结论]慢性 HBV感染者在炎症作用下导致 CD8+ T 细胞内 LAG-3 表达水平增高,而 LAG-3 能通过影响 IL-10、HLA-DR、IFN-γ、T-bet的表达,下调CD8+T对 IFN-γ的分泌量,致T细胞消耗量增加.
Expression Characteristics and Clinical Significance of LAG-3 in CD8+ T Cells from Patients with Chronic Hepatitis B Virus Infection
[Objective]To investigate the expression characteristics and clinical significance of LAG-3 in CD8+T cells from patients with chronic hepatitis B virus(HBV)infection.[Methods]A total of 60 patients with chronic HBV admitted to our hospital from April 2019 to April 2020 were selected as the HBV group.While 60 health examinees in our hospital during the same period were selected as the control group.Blood samples were collected from both groups.The expression level,intensity and frequency of LAG-3 in CD8+T cells were measured by flow cytometry.The expression levels of inter-leukin-10(IL-10),human leukocyte antigen-DR(HLA-DR),interferon-γ(IFN-γ)and transcription factor T-bet(T-bet)were measured.The mechanism of LAG-3 in regulating CD8+T cells was analyzed.[Results]The expression level and in-tensity of LAG-3 in the HBV group were higher than those in the control group(P<0.05).The expression of IL-10 in the LAG-3 positive subgroup was higher than that in LAG-3 negative subgroup within HBV group,and the expression of IL-10 in the LAG-3 negative and positive subgroups within HBV group was higher than that in the control group(P<0.05).The expression of HLA-DR in LAG-3 positive subgroup was lower than that in LAG-3 negative subgroup within HBV group,and the expression of HLA-DR in the LAG-3 negative and positive subgroups within HBV group was lower than that in the control group(P<0.05).The expression of IFN-gamma in the LAG-3 positive subgroup within HBV group was lower than that in the LAG-3 negative subgroup,and the expression of IFN-gamma in the LAG-3 negative and positive subgroups within HBV group was lower than that in the control group(P<0.05).The expression of T-bet in the LAG-3 positive subgroup of HBV group was lower than that in the LAG-3 negative subgroup,and the expression of IFN-gamma in negative and positive subgroups of HBV group was lower than that in the control group(P<0.05).[Conclusion]Chronic HBV infection results in the increase of LAG-3 in CD8+T cells under the actionof inflammation.LAG-3 can reduce the se-cretion of IFN-gamma by affecting the expression of IL-10,HLA-DR,IFN-gamma and T-bet,and increase the consump-tion of T cells.

Hepatitis B,ChronicT-Lymphocyte SubsetsGenes

张闯、申红

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西安高新医院 呼吸科,陕西 西安 710077

西安高新医院 感染性疾病科,陕西 西安 710077

乙型肝炎,慢性 T淋巴细胞亚群 基因

2024

医学临床研究
湖南省医学会

医学临床研究

影响因子:0.595
ISSN:1671-7171
年,卷(期):2024.41(2)
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