期刊文献+

艾滋病患者抗反转录病毒治疗后外周血辅助性和调节性T淋巴细胞的变化及意义 被引量:9

Variation and significance of helper T cells and regulatory T cells in the peripheral blood before and after antiretroviral treatment of human immunodeficiency virus-1 infected patients
原文传递
导出
摘要 目的 探讨艾滋病患者抗反转录病毒治疗(ART)后外周血Th22、Th17、Th1和Treg的变化及其意义.方法 通过流式细胞仪检测40例艾滋病患者ART前及治疗后3个月外周血Th22、Th17、Th1、Treg表达情况.同时选取30名健康人作为对照.组间比较先行方差齐性检验,再行配对t检验,相关性分析采用Spearman rank检验.结果 治疗前艾滋病患者外周血Th22、Th17和Th1均低于健康对照者,分别为(0.59±0.47)%比(1.65±0.56)% (t=8.544,P<0.01)、(4.46±1.84)%比(6.98±1.86)%(t=5.619,P<0.01)和(16.75±6.72)%比(22.77±6.87)%(t=5.311,P<0.01).治疗3个月后,Th22、Th17分别为(1.60±1.10)%(t=5.268,P<0.01)和(6.33±2.64)%(t=3.663,P<0.01),与治疗前比较差异有统计学意义,与健康对照者比较,差异无统计学意义(t值分别为1.783、1.143,均P>0.05);而Th1治疗前后无显著变化,仍低于健康对照者.治疗前艾滋病患者外周血Treg高于健康对照者,为(10.76±3.76)%比(7.01±1.88)%,差异有统计学意义(t=5.003,P<0.01);治疗2个月时降为(9.22±2.56)%,治疗3个月时降为(8.57±2.36)%,但仍高于健康对照者(t=2.984,P=0.004).治疗前艾滋病患者外周血Th22/Treg、Th17/Treg、Th1/Treg的比值均显著低于健康对照者,分别为0.05±0.03比0.25±0.10(t=11.69,P<0.01)、0.46±0.27比1.07±0.42(t=7.728,P<0.01)和1.56±0.89比3.37±1.02(t=7.052,P<0.01).治疗3个月时Th22/Treg、Th17/Treg、Th1/Treg的比值分别为0.17±0.10(t=6.852,P<0.01)、0.81±0.46(t=4.253,P<0.01)和2.31±1.27(t=3.030,P<0.01),与治疗前比较差异有统计学意义.相关性分析显示艾滋病患者外周血Th17/Treg比值与CD4+T淋巴细胞呈正相关(r=0.312 5,P=0.049 6),与HIV RNA呈显著负相关(r=-0.474 7,P=0.002 0).Th1/Treg比值与CD4+T淋巴细胞呈正相关(r=0.333 5,P=0.035 5).结论 艾滋病患者Th22、Th17、Th1与Treg免疫与CD4+T淋巴细胞密切相关,ART可部分恢复免疫功能. Objective To investigate the changes and clinical significance of helper T cells (Th)22,Th17,Th1 and regulatory T cells (Treg) in the peripheral blood before and after antiretroviral treatment (ART) of human immunodeficiency virus (HIV)-1 infected patients.Methods Forty HIV-infected patients were recruited into this study,and 30 healthy subjects were recruited as controls.Peripheral blood of the patients was collected at baseline and after 3 months of ART treatment.The frequencies of Th22,Th17,Th1 and Treg were detected by flow cytometry.Tests for homogeneity of variance and paired t test for comparison was adopted.Spearman rank test was used for correlation analysis.Results The frequencies of peripheral Th22,Th17,Th1 and Treg from HIV-infected patients before treatment were significantly decreased compared to the healthy controls ([0.59± 0.47] % vs [1.65 ± 0.56] % [t =8.544,P<0.01],[4.46±1.84]% vs [6.98±1.86]%[t=5.619,P<0.01],and [16.75±6.72]% vs [22.77±6.87]%; [t=5.311,P<0.01].The frequencies of peripheral Th22 and Th17 after 3 months of treatment were significantly higher than those at baseline ([1.60± 1.10] % [t=5.268,P<0.01] and [6.33±2.64]% [t=3.663,P<0.01] and no difference from those of healthy controls (t=1.783 and 1.143,respectively; both P>0.05).However,the Th1 frequency showed no difference compared to the baseline.The frequency of Treg in the HIV infected patients was significantly increased compared with the healthy controls ([10.76±3.76]% vs [7.01±1.88]%,t=5.003,P<0.01).However,it gradually decreased along with the ART treatment ([9.22±2.56]% after 2 months; [8.57± 2.36]% after 3 months),which was still higher than that of healthy controls (t=2.984,P=0.004).The ratios of Th22/Treg,Th17/Treg and Th1/Treg of the HIV-infected patients were significantly decreased in comparison with the healthy controls (0.05±0.03 vs 0.25±0.10,t=11.69,P<0.01; 0.46 ± 0.27 vs 1.07±0.42,t=7.728,P<0.01; 1.56±0.89 vs 3.37± 1.02,t=7.052,P<0.01),and those were significantly increased after 3 months of treatment (0.17±0.10[t=6.852,P<0.01],0.81±0.46[t=4.253,P<0.01] and 2.31±1.27[t=3.030,P<0.01]).Correlation analysis showed that the ratio of Th17/Treg of the HIV-infected patients was positively correlated with the peripheral CD4+ T cell count (r=0.312 5,P=0.049 6),and negatively correlated with HIV RNA viral load (r=-0.474 7,P=0.002 0).The ratio of Th1/Treg of the HIV-infected patients was positively correlated with the peripheral CD4+ T cell count (r=0.333 5,P=0.035 5).Conclusions Th22,Th17,Th1 and Treg cells in the peripheral blood of HIV-infected patients are closely related to CD4+ T cell count.ART can partially recover immune imbalance,and help to rebuild immune function of HIV-infected patients.
出处 《中华传染病杂志》 CAS CSCD 北大核心 2015年第1期25-29,共5页 Chinese Journal of Infectious Diseases
基金 广东省自然科学基金资助项目(S2012020010873) 感染病国家临床重点学科和深圳市新发传染病重点专科、深圳市科技创新基金资助项目(JCYJ20120829093552348)
关键词 获得性免疫缺陷综合征 抗反转录病毒治疗 T淋巴细胞 调节性 TH22细胞 Th17细胞 TH1细胞 Acquired immunodeficiency syndrome Antiretroviral therapy T-Lymphocytes,regulatory Th22 Th17 Th1
  • 相关文献

参考文献15

  • 1Singh A, Vajpayee M, Ali SA, et al. Cellular interplay among ThlT, Thl, and Treg cells in HIV 1 subtype "C" infection [J]. J MedVirol, 2014,86(3) :372-384.
  • 2彭巧丽,张明霞,李桂英,刘映霞,周伯平,王辉.HIV/AIDS患者体内Th17及Th1应答失衡[J].中华实验和临床病毒学杂志,2010(1):17-20. 被引量:13
  • 3刘映霞,杨桂林,周泱,张红梅,张洁云,王思苑,刘艳,刘水腾,张路坤,王辉.HIV/TB重叠感染者HAART治疗前后Th17/Treg免疫调节的初步研究[J].中华实验和临床病毒学杂志,2011,25(5):348-350. 被引量:4
  • 4Weber GF, Gaertner FC, Erl W,et al. IL 22-mediated tumor growth reduction correlates with inhibition of ERK1/2 and AKT phosphorylation and induction of ceil cycle arrest in the G2-Mphase [J]. J Immunol, 2006,177(11):8266-8272.
  • 5Kim CJ, Nazli A, Rojas OL,et al. A role for mucosal IL-22 production and Th22 cells in HIV-associated mucosal immunopathogenesis [J]. Mucosal Immunol, 2012,5(6) :670- 680.
  • 6E1 Hed A, Khaitan A, Kozhaya L, et al. Susceptibility of human Th17 cells to human immunodeficiency virus and their perturbation during infection [J]. J Infect Dis, 2010,201 (6) 843-854.
  • 7Brenchley JM, Price DA, Schacker TW, et al. Microbial translocation is a cause of systemic immune activation in chronic HIV infection [J]. Nat Med, 2006, 12 (12) :1365- 1371.
  • 8He Y, Li J, Zheng Y, et al. A randomized case-control study of dynamic changes in peripheral blood ThlT/Treg cell balance and interleukin-17 levels in highly active antiretroviral-treated HIV type 1/AIDS patients [J]. AIDS Res Hum Retroviruses, 2012,28(4) :339-345.
  • 9Kedzierska K, Crowe SM. Cytokines and HIV-I: interactions and clinical implications [J]. Antivir Chem Chemother, 2001, 12(3) : 133-150.
  • 10Aandahl EM, Michaelsson J, Moretto WJ, et al. Human CD4+ CD25+ regulatory T ceils control T cell responses to human immunodeficiency virus and cytomegalovirus antigens [J]. J Virol, 2004,78(5): 2454-2459.

二级参考文献12

  • 1Kedzierska K,Crowe SM.Cytokines and HIV-1:interactions and clinical implications.Antivir Chem Chemother,2001,12:133-150.
  • 2Bettelli E,Korn T,Kuchroo VK.Th17:the third member of the effector T cell trilogy.Curr Opin Immunol,2007,19:1-6.
  • 3Stoc kinger B,Veldhoen M.Differentiation and function of Th17 T cells.Curr Opin Immunol,2007,19:281-286.
  • 4Bettelli E,M Oukka,VK Kuchroo.T(H)-17 cells in the circle of immunity and autoimmunity.Nat Immunol,2007,8:345-350.
  • 5Hazenberg MD,Otto SA,Van Benthem BH,et al.Persistent immune activation in HIV-1 infection is associated with progression to AIDS.AIDS,2003,17:1881-1888.
  • 6Brenchley JM,DA Price,TW Schacker,et al.Microbial translocationis a cause of systemic immune activation in chronic HIV infection.Nat Med,2006,12:1365-1371.
  • 7Cecchinato V,Trindade CJ,Laurence A,et al.Altered balance between Th17 and Th1 cells at mucosal sites predicts AIDS progression in simian immunodeficiency virus-infected macaques.Mucosal Immunol,2008,1:279-288.
  • 8Brenchley JM,Paiardini M,Knox KS,et al.Differential Th17 CD4 T-cell depletion in pathogenic and nonpathogenic lentiviral infections.Blood,2008,112:2826-2835.
  • 9Macal M,Sankaran S,Chun TW,et al.Effective CD4~+ T-cell restoration in gut-associated lymphoid tissue of HIV-infected patients is associated with enhanced Th17 cells and polyfunctional HIV speci? c T-cell responses.Mucosal Immunol,2008,1:475-488.
  • 10Harrington LE,Hatton RD,Mangan PR,et al.Interleukin 17-producing CD4^+ effector T cells develop via a lineage distinct from the T helper type 1 and 2 lineages.Nat Immunol,2005,6:1123-1132.

共引文献15

同被引文献68

引证文献9

二级引证文献27

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部