Please wait a minute...
文章检索
预防医学  2024, Vol. 36 Issue (4): 277-282    DOI: 10.19485/j.cnki.issn2096-5087.2024.04.001
  论著 本期目录 | 过刊浏览 | 高级检索 |
HIV/AIDS病例抗病毒治疗后免疫重建的影响因素研究
吴虹1, 许珂1, 张兴亮1, 李西婷1, 程伟2
1.杭州市疾病预防控制中心艾滋病性病防制所,浙江 杭州 310021;
2.浙江省疾病预防控制中心,浙江 杭州 310051
Factors affecting immune reconstitution in HIV/AIDS patients after antiretroviral therapy
WU Hong1, XU Ke1, ZHANG Xingliang1, LI Xiting1, CHENG Wei2
1. Department of AIDS/STD Control and Prevention, Hangzhou Center for Disease Control and Prevention,Hangzhou, Zhejiang 310021, China;
2. Zhejiang Provincial Center for Disease Control and Prevention,Hangzhou, Zhejiang 310051, China
全文: PDF(784 KB)  
输出: BibTeX | EndNote (RIS)      
摘要 目的 了解杭州市艾滋病病毒感染者和艾滋病患者(HIV/AIDS)抗病毒治疗后的免疫重建情况及其影响因素,为提高HIV/AIDS病例抗病毒治疗效果,改善其生存质量提供依据。方法 纳入杭州市2016年1月1日—2021年8月31日开始抗病毒治疗、基线CD4+T淋巴细胞(CD4)计数<500个/μL或基线CD4/CD8+T淋巴细胞(CD8)比值<0.8的HIV/AIDS病例为研究对象,通过中国疾病预防控制信息系统收集抗病毒治疗开始至2023年8月31日随访终止期间的资料,包括基本信息、治疗情况、CD4计数和CD4/CD8比值等,分析HIV/AIDS病例的免疫重建情况,治疗后CD4计数≥500个/μL且CD4/CD8比值≥0.8定义为免疫重建良好。采用多因素Cox比例风险回归模型分析免疫重建的影响因素。结果 纳入HIV/AIDS病例3 349例,其中男性3 075例,占91.82%;开始治疗年龄MQR)为31(20)岁;大专及以上学历1 600例,占47.78%;世界卫生组织(WHO)临床分期Ⅰ~Ⅱ期2 455例,占73.31%。免疫重建良好1 368例,占40.85%;2016年开始抗病毒治疗的HIV/AIDS病例免疫重建良好比例最高,为51.90%。多因素Cox比例风险回归分析结果显示,WHO临床分期(Ⅰ~Ⅱ期,HR=2.529,95%CI:2.023~3.162)、治疗及时(HR=1.196,95%CI:1.027~1.394)、初始治疗方案(替诺福韦+拉米夫定+奈韦拉平/依非韦伦,HR=2.185,95%CI:1.891~2.524;整合酶抑制剂,HR=8.509,95%CI:6.706~10.795)、基线CD4/CD8比值(≥0.1,HR:1.600~4.515,95%CI:1.061~6.661)、基线血红蛋白(<90 mg/dL,HR=0.327,95%CI:0.121~0.880)、合并乙肝感染(HR=0.619,95%CI:0.457~0.840)和合并丙肝感染(HR=0.308,95%CI:0.099~0.956)是HIV/AIDS病例抗病毒治疗后免疫重建的影响因素。结论 HIV/AIDS病例抗病毒治疗后免疫重建情况受WHO临床分期、治疗是否及时、初始治疗方案、基线CD4/CD8比值、基线血红蛋白和乙肝/丙肝感染的影响。
服务
把本文推荐给朋友
加入引用管理器
E-mail Alert
RSS
作者相关文章
吴虹
许珂
张兴亮
李西婷
程伟
关键词 艾滋病抗病毒治疗免疫重建影响因素    
AbstractObjective To investigate the immune reconstitution of HIV/AIDS patients and its influencing factors after receiving antiviral therapy (ART) in Hangzhou City, so as to provide insights into improving the treatment effects and quality of life in HIV/AIDS patients. Methods A retrospective cohort of HIV/AIDS patients who began antiviral treatment between January 1, 2016 and August 31, 2021 and had a baseline CD4+T lymphocyte (CD4) counts of less than 500 cells/μL or a baseline CD4/CD8+T lymphocyte (CD8) ratio of less than 0.8 in Hangzhou City was followed up until August 31, 2023. Demographic information, antiviral therapy in formation, CD4 counts, and CD4/CD8 were collected from the Chinese Disease Prevention and Control Information System. A good immune reconstitution was defined as having CD4≥500 cells/μL and CD4/CD8≥0.8. The immune reconstitution status of HIV/AIDS patients were analyzed, and factors affecting immune reconstitution were identified using a multivariable Cox proportional risk regression model. Results A total of 3 349 HIV/AIDS patients were enrolled, with a median age at ART of 31 (interquartile range, 20) years. There were 3 075 males (91.82%), 1 600 cases with college education and above (47.78%) and 2 455 cases at WHO clinical stage Ⅰ-Ⅱ(73.31%). There were 1 368 cases with good immune reconstitution, accounting for 40.85%, and the proportion of HIV/AIDS patients with good immune reconstitution that began ART in 2016 was the highest, reaching 51.90%. Multivariable Cox proportional risk regression model identified WHO clinical stage (Ⅰ-Ⅱ, HR=2.529, 95%CI: 2.023-3.162), timely ART (HR=1.196, 95%CI: 1.027-1.394), initial treatment regimen (TDF+3TC+NVP/EFV, HR=2.185, 95%CI: 1.891-2.524; integrase inhibitors, HR=8.509, 95%CI: 6.706-10.795), baseline CD4/CD8 (≥0.1, HR: 1.600-4.515, 95%CI: 1.061-6.661), baseline hemoglobin (<90 mg/dL, HR=0.327, 95%CI: 0.121-0.880), hepatitis B infection (HR=0.619, 95%CI: 0.457-0.840) and hepatitis C infection (HR=0.308, 95%CI: 0.099-0.956) as factors affecting immune reconstitution in HIV/AIDS patients. Conclusion The immune reconstitution in HIV/AIDS patients after ART is associated with WHO clinical stage, timely ART, initial treatment regimen, baseline CD4/CD8, baseline hemoglobin and hepatitis B or C infection.
Key wordsAIDS    antiretroviral therapy    immune reconstruction    influencing factor
收稿日期: 2023-12-22      修回日期: 2024-02-27      出版日期: 2024-04-10
中图分类号:  R512.91  
基金资助:杭州市卫生科技计划一般(A类)项目(A20210346); 浙江省科技计划项目(2024C35088); 浙江省医药卫生科技计划项目(2020KY777)
作者简介: 吴虹,硕士,主管医师,主要从事艾滋病防制工作
通信作者: 程伟,E-mail:wcheng@cdc.zj.cn   
引用本文:   
吴虹, 许珂, 张兴亮, 李西婷, 程伟. HIV/AIDS病例抗病毒治疗后免疫重建的影响因素研究[J]. 预防医学, 2024, 36(4): 277-282.
WU Hong, XU Ke, ZHANG Xingliang, LI Xiting, CHENG Wei. Factors affecting immune reconstitution in HIV/AIDS patients after antiretroviral therapy. Preventive Medicine, 2024, 36(4): 277-282.
链接本文:  
https://www.zjyfyxzz.com/CN/10.19485/j.cnki.issn2096-5087.2024.04.001      或      https://www.zjyfyxzz.com/CN/Y2024/V36/I4/277
[1] LIMA V D,REUTER A,HARRIGAN P R,et al.Initiation of antiretroviral therapy at high CD4+cell counts is associated with positive treatment outcomes[J].AIDS,2015,29(14):1871-1882.
[2] LIU P T,TANG Z Z,LAN G H,et al.Early antiretroviral therapy on reducing HIV transmission in China:strengths,weaknesses and next focus of the program[J].Sci Rep,2018,8(1):1-7.
[3] 郑锦雷,潘晓红,马瞧勤,等.MSM人群HIV/AIDS基线CD4水平与艾滋病抗病毒治疗效果的关系研究[J].预防医学,2017,29(12):1189-1192,1198.
[4] TARANCON-DIEZ L,RULL A,HERRETO P,et al.Early antiretroviral therapy initiation effect on metabolic profile in vertically HIV-1-infected children[J].J Antimicrob Chemother,2021,76(11):2993-3001.
[5] YANG X D,SU B,ZHANG X,et al.Incomplete immune reconstitution in HIV/AIDS patients on antiretroviral therapy:challenges of immunological non-responders[J].J Leukoc Biol,2020,107(4):597-612.
[6] 杨小东,粟斌,张彤.HIV-1感染者免疫重建不良研究进展[J].国际病毒学杂志,2020,27(1):82-85.
[7] 陈素庭,洪航,方挺,等.宁波市2010—2020年抗病毒治疗HIV/AIDS免疫重建情况及影响因素分析[J].中华流行病学杂志,2023,44(1):133-138.
[8] KUFA T,SHUBBER Z,MACLEOD W,et al.CD4 count recovery and associated factors among individuals enrolled in the South African antiretroviral therapy programme:an analysis of national laboratory based data[J].PLoS One,2019,14(5):1-15.
[9] ROUL H,MARY-KRAUSE M,GHOSN J,et al.CD4+cell count recovery after combined antiretroviral therapy in the modern combined antiretroviral therapy era[J].AIDS,2018,32(17):2605-2614.
[10] 李国贤,韦慧芬,颜海燕,等.HIV感染者/AIDS患者基线指标对抗病毒治疗后免疫功能重建的影响研究[J].重庆医学,2023,52(18):2751-2757.
[11] LI X L,DING H B,GENG W Q,et al.Predictive effects of body mass index on immune reconstitution among HIV-infected HAART users in China[J].BMC Infect Dis,2019,19(1):1-9.
[12] MA Y,ZHANG F J,ZHAO Y,et al.Cohort profile:the Chinese national free antiretroviral treatment cohort[J].Int J Epidemiol,2010,39(4):973-979.
[13] ZHAO Y,MCGOOGAN J M,WU Z Y.The benefits of immediate ART[J].J Int Assoc Provid AIDS Care,2019,18:1-4.
[14] 吴虹,陈珺芳,许珂,等.2004—2020年杭州市艾滋病抗病毒治疗延迟的影响因素分析[J].预防医学,2021,33(12):1246-1248.
[15] 张昕,张纪元,王福生.晚期AIDS病人HAART后免疫重建的研究进展[J].中国艾滋病性病,2016,22(4):299-304.
[16] LIU J Y,WANG L F,HOU Y Y,et al.Immune restoration in HIV-1-infected patients after 12 years of antiretroviral therapy:a real-world observational study[J].Emerg Microbes Infect,2020,9(1):2550-2561.
[17] 王思苑,孙丽琴,段司沁,等.CD4/CD8比值在HIV感染者中临床分析及其预测价值[J].新发传染病电子杂志,2019,4(2):91-96.
[18] HOCQUELOUX L,AVETTAND-FENOEL V,JACQUOT S,et al.Long-term antiretroviral therapy initiated during primary HIV-1 infection is key to achieving both low HIV reservoirs and normal T cell counts[J].J Antimicrob Chemother,2013,68(5):1169-1178.
[19] 俞海亮,杨跃诚,赵燕,等.德宏傣族景颇族自治州成年人HIV/AIDS抗病毒治疗后CD4+T淋巴细胞免疫重建及影响因素分析[J].中华流行病学杂志,2021,42(6):1050-1055.
[20] SERRANO-VILLAR S,ZHOU Y,RODGERS A J,et al.Different impact of raltegravir versus efavirenz on CD4/CD8 ratio recovery in HIV-infected patients[J].J Antimicrob Chemother,2017,72(1):235-239.
[21] 梅馨尹,王佳洁,劳晓洁,等.广西艾滋病患者免疫重建不良的预测模型建立[J].中国艾滋病性病,2021,27(12):1348-1352.
[22] LINCOLN D,PETOUMENOS K,DORE G J.HIV/HBV and HIV/HCV coinfection,and outcomes following highly active antiretroviral therapy[J].HIV Med,2003,4(3):241-249.
[23] SILVA C,PEDER L D,SILVA E S,et al.Impact of HBV and HCV coinfection on CD4 cells among HIV-infected patients:a longitudinal retrospective study[J].J Infect Dev Ctries,2018,12(11):1009-1018.
[24] RALLON N I,LOPEZ M,SORIANO V,et al.Level,phenotype and activation status of CD4+FoxP3+regulatory T cells in patients chronically infected with human immunodeficiency virus and/or hepatitis C virus[J].Clin Exp Immunol,2009,155(1):35-43.
[1] 吕婧, 徐欣颖, 乔颖异, 石兴龙, 岳芳, 刘营, 程传龙, 张宇琦, 孙继民, 李秀君. 浙江省发热伴血小板减少综合征流行特征及影响因素分析[J]. 预防医学, 2026, 38(1): 10-14.
[2] 吴成慧, 彭艳红, 张可, 朱维晔, 邓亮, 谭玲玲, 瞿丹丹, 米秋香. 中青年2型糖尿病患者益处发现的影响因素分析[J]. 预防医学, 2026, 38(1): 31-35.
[3] 徐光明, 张震, 叶小红. 2015—2024年临海市新报告HIV/AIDS病例晚发现及影响因素分析[J]. 预防医学, 2026, 38(1): 71-74.
[4] 夏子淇, 陈晴晴, 高四海, 吴矛矛. 温州市中小学生营养健康知识调查[J]. 预防医学, 2026, 38(1): 98-101,106.
[5] 陈慧, 苗姗姗, 刘宪峰, 张慧. 新疆生产建设兵团中小学生龋齿现况调查[J]. 预防医学, 2026, 38(1): 102-106.
[6] 陶桃, 张海芳, 凡鹏飞, 李秋华, 陈晓蕾. 丽水市老年肺结核患者治疗转归的影响因素分析[J]. 预防医学, 2025, 37(9): 892-896,902.
[7] 徐艳平, 闫晓彤, 姚丁铭, 徐越, 张雪海, 孙洁, 徐锦杭. 浙江省中老年人肺炎疫苗接种意愿的影响因素研究[J]. 预防医学, 2025, 37(9): 881-885.
[8] 姜艳, 李锦成, 许纯, 杨科佼, 杨文彬, 徐胜. 扬州市MSM人群艾滋病非职业暴露后预防知晓率调查[J]. 预防医学, 2025, 37(9): 903-906,912.
[9] 翟羽佳, 章涛, 古雪, 徐乐, 吴梦娜, 林君芬, 吴晨. 社区老年人认知衰弱现况调查[J]. 预防医学, 2025, 37(8): 762-766,772.
[10] 苏德华, 陈向阳, 李君, 赵丽娜, 张鹤美, 朱婷婷, 胡文雪, 赖江宜. 温州市新报告HIV/AIDS病例抗病毒治疗及时性分析[J]. 预防医学, 2025, 37(8): 804-808.
[11] 徐莉, 刘萍, 卞宇旬, 陈圆媛, 李鑫娜, 周乐. 扬州市新报告50岁及以上HIV/AIDS病例抗病毒治疗前耐药分析[J]. 预防医学, 2025, 37(8): 779-782,788.
[12] 严青秀, 王炜, 郝晓刚, 高宇, 方春福, 张幸, 刘文峰. 2017—2023年衢州市肺结核患者未收治情况分析[J]. 预防医学, 2025, 37(8): 799-803.
[13] 王晓宇, 张志平, 董玉颖, 梁杰, 陈强. 老年人带状疱疹疫苗接种意愿的影响因素分析[J]. 预防医学, 2025, 37(8): 809-813.
[14] 王海琪, 张涵潇, 杨凤云, 国献丽, 范生荣, 张丽锋, 蒋泓. 嘉定区中学生抑郁情绪调查[J]. 预防医学, 2025, 37(8): 832-836.
[15] 成灵灵, 阎亚琼, 白增华, 张晓刚, 郝丽婷, 杨慧莹. 先天性甲状腺功能减退症患儿年龄别体质指数Z评分变化轨迹及影响因素[J]. 预防医学, 2025, 37(8): 858-863.
Viewed
Full text


Abstract

Cited

  Shared   
  Discussed