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HIV/HBV感染患者血清sPD-L1、sFas表达水平及临床意义

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目的 研究人类免疫缺陷病毒(HIV)/乙型肝炎病毒(HBV)合并感染患者血清可溶性程序性死亡因子配体-1(sPD-L1)、可溶性凋亡相关因子(sFas)表达水平及临床意义.方法 选取2018年2月-2021年2月期间贵州航天医院诊治的138例HBV感染患者为研究对象,根据是否合并HIV感染分为HIV/HBV组(HIV/HBV合并感染,n=60)和HBV组(单纯HBV感染,n=78),以同期于本院健康体检的50名健康人群为对照组.酶联免疫吸附实验检测各组血清sPD-L1、sFas水平.Pearson相关分析血清sPD-L1、sFas水平与临床指标的相关性.多因素logistic回归分析影响HIV/HBV合并感染的因素.受试者工作特征曲线分析血清sPD-L1、sFas单独及联合检测对HIV/HBV合并感染的诊断价值.结果 HIV/HBV组患者血清丙氨酸氨基转移酶、天门冬氨酸氨基转移酶、sPD-L1、sFas、肿瘤坏死因子-α(TNF-α)及白细胞介素-6(IL-6)明显高于HBV组和对照组,差异均有统计学意义(P均<0.05);且HBV组患者血清丙氨酸氨基转移酶、天门冬氨酸氨基转移酶、sPD-L1、sFas、TNF-α及IL-6明显高于对照组,差异均有统计学意义(P均<0.05);以上指标3组间比较,差异均有统计学意义(F=682.191、1 149.180、166.771、437.213、382.011、754.180,P均<0.05).HIV/HBV合并感染患者血清sPD-L1、sFas水平与HIV RNA、HBV DNA、丙氨酸氨基转移酶、天门冬氨酸氨基转移酶、TNF-α 及 IL-6 成正相关(r=0.640、0.701、0.534、0.551、0.603、0.615,0.617、0.653、0.498、0.434、0.701、0.723,P均<0.05),与外周血CD4+T淋巴细胞计数成负相关(r=-0.662、-0.669,P均<0.05).sPD-L1、sFas升高是影响HIV/HBV合并感染的独立危险因素(P均<0.05).血清sPD-L1、sFas联合检测对HIV/HBV合并感染诊断的曲线下面积为0.893,高于sPD-L1、sFas单独检测的0.820、0.721,差异均有统计学意义(Z=2.302、4.918,P均<0.05).结论 HIV/HBV合并感染患者血清sPD-L1、sFas水平升高,是影响HIV/HBV合并感染发生的独立危险因素,血清sPD-L1、sFas联合检测对HIV/HBV合并感染具有较高的诊断价值.
The expression and clinical significance of sPD-L1 and sFas in serum of HIV/HBV infected patients
Objective To study the expression and clinical significance of soluble programmed death factor ligand-1(sPD-L1)and soluble apoptosis related factor(sFas)in the serum of patients with human immunodeficiency virus/hepatitis B virus(HIV/HBV)coinfection.Methods A total of 138 HBV infected patients who were diagnosed and treated in the Guizhou Aerospace Hospital from February 2018 to February 2021 were selected as the research subjects.They were divided into the HIV/HBV group(HIV/HBV coinfection,n=60)and the HBV group(simple HBV infection,n=78).A total of 50 healthy individuals who underwent physical examinations in our hospital during the same period were used as the control group.Enzyme linked immunosorbent assay was used to detect serum sPD-L1 and sFas levels in each group.Pearson correlation analysis was used to analyze the correlation between serum sPD-L1,sFas levels and clinical indicators.Multivariate logistic regression analysis was conducted to investigate the factors influencing the co infection of HIV/HBV.The diagnostic value of sPD-L1,sFas and combined detection in the diagnosis of HIV/HBV coinfection by analyzing the receiver operating characteristic curve of subjects.Results The levels of serum alanine transaminase,aspartate transaminase,sPD-L1,sFas,tumor necrosis factor-α(TNF-α)and interleukin-6(IL-6)in HIV/HBV group were significantly higher than those in HBV group and control group(all P<0.05);the levels of serum alanine transaminase,aspartate transaminase,sPD-L1,sFas,TNF-α and IL-6 in HBV group were significantly higher than those in control group(all P<0.05).There were significant differences in the above indexes among the three groups(F=682.191,1 149.180,166.771,437.213,382.011,754.180;all P<0.05).There was a significant positive correlation between serum sPD-L1,sFas levels and HIV RNA,HBV DNA,alanine transaminase,aspartate transaminase,TNF-α,IL-6 in patients with HIV/HBV coinfection(r=0.640,0.701,0.534,0.551,0.603,0.615;0.617,0.653,0.498,0.434,0.701,0.723;all P<0.05),while a significant negative correlation with peripheral blood CD4+T lymphocyte count(r=-0.662,-0.669;both P<0.05).sPD-L1,sFas were independent risk factors for HIV/HBV coinfection(both P<0.05).The area under the curve of serum sPD-L1 and sFas combined detection for the diagnosis of HIV/HBV coinfection was 0.893,which was significantly higher than that of serum sPD-L1 and sFas alone(0.820,0.721)(Z=2.302,4.918,both P<0.05).Conclusions The serum levels of sPD-L1 and sFas in patients with HIV/HBV coinfection were elevated,which were independent risk factors for HIV/HBV coinfection.The combined detection of serum sPD-L1 and sFas had high diagnostic value for HIV/HBV coinfection.

Human immunodeficiency virusHepatitis B virusSoluble programmed death factor ligand-1Soluble apoptosis related factor

刘靓、熊玮、龙鑫

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贵州航天医院(遵义医科大学附属航天医院)疾控门诊,贵州遵义 563000

贵州航天医院(遵义医科大学附属航天医院)感染科,贵州遵义 563000

人类免疫缺陷病毒 乙型肝炎病毒 可溶性程序性死亡因子配体-1 可溶性凋亡相关因子

贵州省卫生健康委科学技术基金项目

gzwjkj2019-1-073

2024

热带医学杂志
广东省寄生虫学会 中华预防医学会

热带医学杂志

CSTPCD
影响因子:0.643
ISSN:1672-3619
年,卷(期):2024.24(9)