hiv感染和未感染注射吸毒者的行为、粘膜和全身免疫参数

S. Mehandru, S. Deren, S. Kang, A. Banfield, A. Garg, D. Garmon, M. Lamar, Teresa H. Evering, M. Markowitz
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引用次数: 16

摘要

目的注射吸毒(IDU)仍然是HIV-1感染的主要危险因素。药物使用、非无菌注射和丙型肝炎之间复杂的相互作用仍然知之甚少。我们进行了一项初步研究,以确定IDU对hiv未感染和感染个体免疫参数的影响。我们假设IDU可以进一步增强与HIV-1感染相关的免疫变化,进而影响HIV的发病机制方法招募未感染HIV和感染HIV的IDU受试者以及未IDU对照组,以获得社会人口统计学和药物相关行为。分析血液(PBMC)和粘膜(MMC)单核细胞免疫激活的细胞标志物(CD38和Ki67)。血清ELISA测定可溶性CD14水平,这是免疫激活的标志。结果在考虑HIV-1感染的情况下,IDU和非IDU受试者的CD4+和CD8+ T细胞水平没有显著的定量差异。然而,与非注射者相比,未感染hiv的IDU受试者的细胞和血浆中免疫激活的细胞和可溶性标志物水平升高。此外,共用注射用具与未感染艾滋病毒的IDU受试者的免疫激活有关。结论IDU无论是否感染HIV-1,都能显著提高外周血和胃肠道的免疫活性。这可能对艾滋病毒的传播、发病机制和对联合抗病毒治疗的免疫反应有重大影响。这项研究提供了令人信服的初步结果,反过来支持更大规模的研究,以更好地定义IDU、HIV-1感染、丙型肝炎合并感染和免疫之间的关系。
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Behavioural, Mucosal and Systemic Immune Parameters in HIV-infected and Uninfected Injection Drug Users
Objective Injection drug use (IDU) remains a major risk factor for HIV-1 acquisition. The complex interplay between drug use, non-sterile injection, and Hepatitis C remains poorly understood. We conducted a pilot study to determine the effect of IDU on immune parameters among HIV-uninfected and -infected individuals. We hypothesized that IDU could further augment immunological changes associated with HIV-1 infection, which could in turn affect HIV pathogenesis Methods HIV-uninfected and -infected subjects with IDU, and non-IDU controls were recruited to obtain socio-demographic and drug-related behaviours. Blood (PBMC) and mucosal (MMC) mononuclear cells were analysed for cellular markers of immune activation (CD38 and Ki67). Serum ELISA was performed to determine levels of soluble CD14, a marker of immune activation. Results No significant quantitative differences in CD4+ and CD8+ T cell levels were observed between IDU and non-IDU subjects when accounting for the presence of HIV-1 infection. However, increased levels of cellular and soluble markers of immune activation were documented in cells and plasma of HIV-uninfected IDU subjects compared to non-injectors. Additionally, sharing of injection paraphernalia was related to immune activation among HIV-uninfected IDU subjects. Conclusion IDU, with or without HIV-1 infection, results in a significant increase in immune activation in both the peripheral blood and the GI tract. This may have significant impact on HIV transmission, pathogenesis, and immunologic responses to combination antiviral therapy. This study provides compelling preliminary results which in turn support larger studies to better define the relationship between IDU, infection with HIV-1, co-infection with Hepatitis C and immunity.
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