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吸烟会增加接受抗逆转录病毒治疗的HIV感染患者的免疫激活并损害其T细胞功能:一项横断面试点研究。

Tobacco smoking increases immune activation and impairs T-cell function in HIV infected patients on antiretrovirals: a cross-sectional pilot study.

作者信息

Valiathan Ranjini, Miguez Maria J, Patel Bijal, Arheart Kristopher L, Asthana Deshratn

机构信息

Department of Pathology, University of Miami-Miller School of Medicine, Miami, Florida, United States of America; Laboratory for Clinical and Biological Studies, University of Miami-Miller School of Medicine, Miami, Florida, United States of America.

School of Integrated Science and Humanities, Florida International University, Miami, Florida, United States of America.

出版信息

PLoS One. 2014 May 19;9(5):e97698. doi: 10.1371/journal.pone.0097698. eCollection 2014.

Abstract

BACKGROUND

The influence of tobacco smoking on the immune system of HIV infected individuals is largely unknown. We investigated the impact of tobacco smoking on immune activation, microbial translocation, immune exhaustion and T-cell function in HIV infected individuals.

METHOD

HIV infected smokers and non-smokers (n = 25 each) with documented viral suppression on combination antiretroviral therapy and HIV uninfected smokers and non-smokers (n = 15 each) were enrolled. Markers of immune activation (CD38 and HLA-DR) and immune exhaustion (PD1, Tim3 and CTLA4) were analyzed in peripheral blood mononuclear cells (PBMCs) by flow cytometry. Plasma markers of microbial translocation (soluble-CD14 - sCD14 and lipopolysaccharide - LPS) were measured. Antigen specific functions of CD4+ and CD8+ T-cells were measured, by flow cytometry, in PBMCs after 6 hours stimulation with Cytomegalovirus, Epstein-Barr virus and Influenza Virus (CEF) peptide pool.

RESULTS

Compared to non-smokers, smokers of HIV infected and uninfected groups showed significantly higher CD4+ and CD8+ T-cell activation with increased frequencies of CD38+HLA-DR+ cells with a higher magnitude in HIV infected smokers. Expressions of immune exhaustion markers (PD1, Tim3 and CTLA4) either alone or in combinations were significantly higher in smokers, especially on CD4+ T-cells. Compared to HIV uninfected non-smokers, microbial translocation (sCD14 and LPS) was higher in smokers of both groups and directly correlated with CD4+ and CD8+ T-cell activation. Antigen specific T-cell function showed significantly lower cytokine response of CD4+ and CD8+ T-cells to CEF peptide-pool stimulation in smokers of both HIV infected and uninfected groups.

CONCLUSIONS

Our results suggest that smoking and HIV infection independently influence T-cell immune activation and function and together they present the worst immune profile. Since smoking is widespread among HIV infected individuals, studies are warranted to further evaluate the cumulative effect of smoking on impairment of the immune system and accelerated disease progression.

摘要

背景

吸烟对HIV感染者免疫系统的影响在很大程度上尚不清楚。我们调查了吸烟对HIV感染者免疫激活、微生物易位、免疫耗竭和T细胞功能的影响。

方法

纳入接受联合抗逆转录病毒治疗且病毒得到抑制的HIV感染吸烟者和非吸烟者(各25例)以及未感染HIV的吸烟者和非吸烟者(各15例)。通过流式细胞术分析外周血单个核细胞(PBMC)中免疫激活标志物(CD38和HLA-DR)和免疫耗竭标志物(PD1、Tim3和CTLA4)。检测微生物易位的血浆标志物(可溶性CD14 - sCD14和脂多糖 - LPS)。在用巨细胞病毒、爱泼斯坦 - 巴尔病毒和流感病毒(CEF)肽库刺激6小时后,通过流式细胞术检测PBMC中CD4 +和CD8 + T细胞的抗原特异性功能。

结果

与非吸烟者相比,HIV感染组和未感染组的吸烟者CD4 +和CD8 + T细胞激活显著更高,CD38 + HLA-DR +细胞频率增加,在HIV感染吸烟者中增幅更大。免疫耗竭标志物(PD1、Tim3和CTLA4)单独或联合表达在吸烟者中显著更高,尤其是在CD4 + T细胞上。与未感染HIV的非吸烟者相比,两组吸烟者的微生物易位(sCD14和LPS)更高,且与CD4 +和CD8 + T细胞激活直接相关。在HIV感染组和未感染组的吸烟者中,抗原特异性T细胞功能显示CD4 +和CD8 + T细胞对CEF肽库刺激的细胞因子反应显著更低。

结论

我们的结果表明,吸烟和HIV感染独立影响T细胞免疫激活和功能,二者共同导致最差的免疫状态。由于吸烟在HIV感染者中广泛存在,有必要开展研究以进一步评估吸烟对免疫系统损害和疾病进展加速的累积效应。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a99/4026405/a9fee1ef9704/pone.0097698.g001.jpg

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