Cauda R, Goletti D, Lucia M B, Tumbarello M, Rumi C, Orengo A M, Moretta A
Istituto di Clinica Malattie Infettive, Università Cattolica S. Cuore, Roma, Italy.
Clin Immunol Immunopathol. 1994 Mar;70(3):198-205. doi: 10.1006/clin.1994.1029.
In this study we analyzed the expression of EB6 and GL183, which are part of P58 molecular family that represents the putative NK receptor for MHC class I molecules, in peripheral blood lymphocytes of 60 patients with HIV infection (20 asymptomatic HIV-seropositive individuals, 20 patients with constitutional symptoms, and 20 AIDS patients) and correlated it with the level of CD4+, CD56+ cells, and the NK cell activity in order to determine a possible relation with disease progression. The absolute number (but not the percentage) of CD56+, EB6+, and GL183+ cells was significantly reduced only in AIDS patients but not in the other AIDS-related clinical conditions. On the contrary, NK cell activity was reduced in all HIV-infected patients. In a 6-month follow-up, patients with constant clinical conditions and stable CD4+ cells level showed no significant difference, either in the percentage or absolute number of EB6+ and GL183+ cells. Interestingly, dual-color fluorescence indicates that GL183 and EB6 molecules (that in normal individuals are virtually absent on CD3- NK cells) are expressed in HIV-infected individuals not only in CD56+ cells but also in CD3+ cells. This may reflect a depletion of other T cell subsets or alternatively (less likely) a specific immune response. Our data indicate that the expression of EB6 and GL183 in T and NK cells from HIV-infected patients might be relevant in the course of the disease and for the disease-associated functional defect of NK cell activity.
在本研究中,我们分析了EB6和GL183的表达情况。EB6和GL183是P58分子家族的一部分,该家族代表了假定的MHC I类分子的自然杀伤(NK)受体。我们对60例HIV感染患者(20例无症状HIV血清阳性个体、20例有全身症状的患者和20例艾滋病患者)的外周血淋巴细胞进行了分析,并将其与CD4 +、CD56 +细胞水平以及NK细胞活性相关联,以确定其与疾病进展的可能关系。仅在艾滋病患者中,CD56 +、EB6 +和GL183 +细胞的绝对数量(而非百分比)显著降低,而在其他与艾滋病相关的临床情况中则未降低。相反,所有HIV感染患者的NK细胞活性均降低。在为期6个月的随访中,临床状况稳定且CD4 +细胞水平稳定的患者,其EB6 +和GL183 +细胞的百分比或绝对数量均无显著差异。有趣的是,双色荧光表明,GL183和EB6分子(在正常个体的CD3 - NK细胞上几乎不存在)在HIV感染个体中不仅在CD56 +细胞中表达,而且在CD3 +细胞中也表达。这可能反映了其他T细胞亚群的耗竭,或者(可能性较小)反映了一种特异性免疫反应。我们的数据表明,HIV感染患者的T细胞和NK细胞中EB6和GL183的表达可能与疾病进程以及NK细胞活性的疾病相关功能缺陷有关。