Wang Liqiang, Adegboyega Patrick A
Department of Pathology, The University of Texas Medical Branch, Galveston, TX 77555-0588, USA.
Arch Pathol Lab Med. 2002 Jan;126(1):28-32. doi: 10.5858/2002-126-0028-DROFEI.
The mechanism by which human immunodeficiency virus 1 (HIV-1) infection causes increased rates of apoptosis and gradual chronic depletion of CD4(+) T lymphocytes in patients infected with HIV-1 is not known. Findings from in vitro culture studies and analysis of mononuclear cells in the peripheral blood of HIV-infected patients have led to the hypothesis that abnormal expression and/or interaction of Fas and Fas ligand (FasL) may play significant roles in the derangement of homeostasis of CD4(+) lymphocytes in patients infected with HIV-1.
To determine the in situ expression of Fas and FasL in the lymph nodes of patients infected with HIV-1.
Immunohistochemical expression of Fas and FasL was studied in the lymph node biopsy specimens from 20 patients infected with HIV-1. As controls, we also studied 120 lymph nodes from 28 HIV-1-seronegative patients with reactive lymphadenopathy.
In the reactive lymph nodes of seronegative patients, expression of Fas was diffuse in the germinal centers and also in immunoblast-like cells in the T-cell regions. In the lymph nodes of patients infected with HIV, there was a consistent remarkable decrease in Fas expression in 12 of 20 patients and a total lack of Fas expression in the remaining 8 patients. Expression of FasL was comparable in both patient groups.
There is marked down-regulation of Fas in the lymph nodes of HIV-infected patients, a sharp contrast to what occurs in circulating mononuclear cells in the peripheral blood of these patients. These results indicate the need for further studies of this molecular event for possible therapeutic intervention based on reconstitution of Fas and/or FasL activity in the treatment of HIV infection.
人类免疫缺陷病毒1型(HIV-1)感染导致HIV-1感染患者细胞凋亡率增加和CD4(+) T淋巴细胞逐渐慢性耗竭的机制尚不清楚。体外培养研究以及对HIV感染患者外周血单个核细胞的分析结果提出了一个假说,即Fas和Fas配体(FasL)的异常表达和/或相互作用可能在HIV-1感染患者CD4(+)淋巴细胞稳态紊乱中起重要作用。
确定HIV-1感染患者淋巴结中Fas和FasL的原位表达。
对20例HIV-1感染患者的淋巴结活检标本进行Fas和FasL的免疫组化表达研究。作为对照,我们还研究了28例反应性淋巴结病的HIV-1血清阴性患者的120个淋巴结。
在血清阴性患者的反应性淋巴结中,Fas在生发中心以及T细胞区域的免疫母细胞样细胞中呈弥漫性表达。在HIV感染患者的淋巴结中,20例患者中有12例Fas表达持续显著降低,其余8例患者完全缺乏Fas表达。两组患者的FasL表达相当。
HIV感染患者的淋巴结中Fas明显下调,这与这些患者外周血循环单核细胞中的情况形成鲜明对比。这些结果表明,需要进一步研究这一分子事件,以便在治疗HIV感染时基于Fas和/或FasL活性的重建进行可能的治疗干预。