Carvalho A C C, Matteelli A, Airò P, Tedoldi S, Casalini C, Imberti L, Cadeo G P, Beltrame A, Carosi G
Unidade de Pesquisa em Tuberculose, Serviço de Pneumologia, Hospital Universitário Clementino Fraga Filho/Universidade Federal do Rio de Janeiro (HUCFF/UFRJ), Rio de Janeiro, Brazil.
Thorax. 2002 Apr;57(4):357-60. doi: 10.1136/thorax.57.4.357.
Several recent studies suggest that gammadelta T lymphocytes play an important role in immunity against Mycobacterium tuberculosis. However, the dynamics of these cells in the peripheral blood of patients with tuberculosis (TB) with and without HIV infection is not fully understood. A study was undertaken to evaluate the profile of the gammadelta T cell population in patients at the time the diagnosis of TB was established.
A cross sectional study was performed in consecutive TB patients from the Department of Infectious Diseases, Spedali Civili, Brescia. CD4+, CD8+ and Vdelta1 and Vdelta2 T cell counts were analysed. Lymphocyte surface membrane expression was evaluated with the FITC-TCRgammadelta, -Vdelta1, -Vdelta2 and PE-Vdelta1 monoclonal antibodies. Blood donors and HIV seropositive asymptomatic individuals acted as controls.
Seventy four TB patients were evaluated, 20 of whom (27%) were co-infected with HIV. HIV seronegative TB patients (n=54) had total gammadelta T cells and Vdelta1 subsets comparable to those in blood donors (n=39). However, the percentage with the Vdelta2 subset was significantly lower in patients with TB than in controls (median 1.5 v 2.1; p=0.05). Responsiveness to PPD was not associated with predominance of a specific gammadelta T cell subset. HIV seropositive individuals had a decreased percentage of circulating Vdelta2 cells at a level similar to that in HIV seronegative TB patients, regardless of the presence of active TB.
HIV seronegative TB patients and HIV infected individuals (with or without active TB) have a reduced number of circulating Vdelta2 T cells compared with healthy individuals. Whether TB and HIV infection share a common mechanism causing Vdelta2 T cell depletion still needs to be established.
最近的几项研究表明,γδ T淋巴细胞在抗结核分枝杆菌免疫中发挥重要作用。然而,在合并或未合并HIV感染的结核病(TB)患者外周血中,这些细胞的动态变化尚未完全明确。本研究旨在评估结核病确诊时患者γδ T细胞群体的特征。
对布雷西亚市斯佩达利·奇维利传染病科的连续结核病患者进行横断面研究。分析CD4 +、CD8 +以及Vδ1和Vδ2 T细胞计数。使用异硫氰酸荧光素(FITC)标记的TCRγδ、-Vδ1、-Vδ2和藻红蛋白(PE)标记的Vδ1单克隆抗体评估淋巴细胞表面膜表达。献血者和HIV血清学阳性无症状个体作为对照。
共评估了74例结核病患者,其中20例(27%)合并HIV感染。HIV血清学阴性的结核病患者(n = 54)的总γδ T细胞和Vδ1亚群与献血者(n = 39)相当。然而,结核病患者中Vδ2亚群的百分比显著低于对照组(中位数1.5对2.1;p = 0.05)。对结核菌素纯蛋白衍生物(PPD)的反应性与特定γδ T细胞亚群的优势无关。无论是否存在活动性结核病,HIV血清学阳性个体循环Vδ2细胞的百分比均降低,且降低水平与HIV血清学阴性的结核病患者相似。
与健康个体相比,HIV血清学阴性的结核病患者以及HIV感染个体(无论有无活动性结核病)循环Vδ2 T细胞数量均减少。结核病和HIV感染是否共享导致Vδ2 T细胞耗竭的共同机制仍有待确定。