Gielen V, Schmitt D, Dezutter-Dambuyant C, Thivolet J
Laboratoire de Recherche Dermatologique et Immunologie, INSERM U 209, Hôpital Edouard Herriot, Lyon, France.
Reg Immunol. 1989 Jan-Feb;2(1):7-13.
Langerhans cells (LC) are CD4-positive antigen-presenting cells within the human epidermis and thus potentially may be infected by the causative agent of AIDS (acquired immunodeficiency syndrome), called HIV (human immunodeficiency virus). Because CD4 antigens have been demonstrated to be decreased in HIV-infected lymphocytes, we wondered whether some immunologic markers of LC might be modified in seropositive patients. For this purpose, LC, obtained from clinically unaffected skin of ARC (AIDS-related complex) and AIDS patients, were subjected to anti-CD4 (OKT4) and anti-HLA class II monoclonal antibodies (anti-DR: BL1 and anti-DQ). The density of the antigenic sites/LC recognized by the antibodies was evaluated by employing the electron microscopic immunogold labeling procedure. The density of CD4 molecules/cell measured in LC of ARC and AIDS patients by direct count of gold particles bound to the cell membrane was found to be dramatically decreased among AIDS LC, whereas a small subset of ARC LC strongly expressed this antigen. In contrast, the density of HLA class II (DR and DQ) antigenic determinants was found unchanged in comparison with that of healthy donors. In addition to the quantitative modifications of the CD4 molecule expression by ARC and AIDS LC, the observation in these cell populations of several surface protrusions suggesting viral buds affords evidence that LC are a target for HIV.
朗格汉斯细胞(LC)是人类表皮内的CD4阳性抗原呈递细胞,因此有可能被获得性免疫缺陷综合征(艾滋病)的病原体——人类免疫缺陷病毒(HIV)感染。由于已证实在HIV感染的淋巴细胞中CD4抗原减少,我们想知道在血清反应阳性患者中LC的一些免疫标记是否会发生改变。为此,从艾滋病相关综合征(ARC)和艾滋病患者临床上未受影响的皮肤中获取LC,用抗CD4(OKT4)和抗HLA II类单克隆抗体(抗DR:BL1和抗DQ)进行检测。通过电子显微镜免疫金标记程序评估抗体识别的抗原位点/LC的密度。通过直接计数与细胞膜结合的金颗粒来测量ARC和艾滋病患者LC中CD4分子/细胞的密度,结果发现艾滋病LC中的该密度显著降低,而一小部分ARC LC强烈表达这种抗原。相比之下,与健康供体相比,HLA II类(DR和DQ)抗原决定簇的密度没有变化。除了ARC和艾滋病LC对CD4分子表达的定量改变外,在这些细胞群体中观察到几个表面突起提示病毒芽,这提供了LC是HIV靶标的证据。