Department of Biological Chemistry, University of Buenos Aires, School of Sciences, Buenos Aires, Argentina.
J Int AIDS Soc. 2012 Jun 14;15(2):17428. doi: 10.7448/IAS.15.2.17428.
Tuberculosis (TB) continues to be the most frequent cause of illness and death from an infectious agent globally, and its interaction with HIV is having devastating effects. To investigate how HIV alters the immune response to Mycobacterium tuberculosis (Mtb), we assessed basal and Mtb-induced proliferation, cytokine production, and expression of signalling lymphocytic activation molecule (SLAM), inducible costimulator (ICOS) and programmed death-1 (PD-1) on T lymphocytes from HIV-positive individuals coinfected with TB, HIV-positive subjects, TB patients and healthy donors (HD).
HIV-TB patients showed increased ICOS, SLAM and PD-1 basal levels on T lymphocytes, whereas HIV-positive individuals displayed elevated levels of SLAM and PD-1, TB patients high levels of SLAM, and HD low levels of the three proteins. Mtb-stimulation enhanced ICOS expression in the four groups, but only TB and HD increased SLAM and PD-1 levels.
These data show the immune deregulation that takes place during the immune response against TB in different study populations.
结核病(TB)仍然是全球范围内由感染因子引起的最常见的疾病和死亡原因,其与 HIV 的相互作用产生了毁灭性的影响。为了研究 HIV 如何改变对结核分枝杆菌(Mtb)的免疫反应,我们评估了 HIV 阳性合并结核患者、HIV 阳性个体、结核患者和健康供体(HD)的 T 淋巴细胞的基础增殖和 Mtb 诱导增殖、细胞因子产生以及信号淋巴细胞激活分子(SLAM)、诱导共刺激分子(ICOS)和程序性死亡-1(PD-1)的表达。
HIV-TB 患者的 T 淋巴细胞上的 ICOS、SLAM 和 PD-1 基础水平升高,而 HIV 阳性个体的 SLAM 和 PD-1 水平升高,结核患者的 SLAM 水平升高,HD 的三种蛋白水平降低。Mtb 刺激增强了四个组中的 ICOS 表达,但仅 TB 和 HD 增加了 SLAM 和 PD-1 水平。
这些数据显示了在不同研究人群中针对 TB 的免疫反应过程中发生的免疫失调。