Esterre P, Dedet J P, Frenay C, Chevallier M, Grimaud J A
Laboratoire de Parasitologie, Institut Pasteur de Guyane, Cayenne, French Guiana.
Virchows Arch A Pathol Anat Histopathol. 1992;421(3):239-47. doi: 10.1007/BF01611181.
To characterize the in situ cellular immune response in localized cutaneous leishmaniasis (LCL), the authors studied frozen skin biopsies from 50 patients with LCL due to Leishmania braziliensis guyanensis. A panel of 31 monoclonal antibodies was used, which defined the number and distribution of inflammatory cell subsets. Skin inflammatory infiltrates were composed of T cells (with a local CD4/CD8 ratio of 1.05 +/- 0.7 vs 1.48 +/- 0.3 in peripheral blood), macrophages and a smaller number of B cells, natural killer cells and granulocytes. Most of the T cells expressed activation markers (interleukin-2 and transferrin receptors, HLA-DR+) and an increase in T-cell-receptor gamma delta expression was noted. Analysis of the CD4+ subpopulations with newly available reagents showed that helper T cells (CD4+CD45RO+) exceeded the suppressor/inducer subset (CD4+CD45RA+) by 1.4:1. There were no differences between local immune variables from patients with primary infection (45 patients) and those with recurrence (5). In 7 patients, biopsies were analysed before and 1 month after specific treatment, and did not show significant differences except for a small increase of dermal CD1a+ (Langerhans) cells/mm2. The observed pattern of cellular skin infiltration suggests an immune-mediated tissue injury including T-cell-mediated cytotoxicity and delayed hypersensitivity reactions in addition to direct parasitic action.
为了描述局限性皮肤利什曼病(LCL)中的原位细胞免疫反应,作者研究了50例因圭亚那利什曼原虫引起的LCL患者的冷冻皮肤活检样本。使用了一组31种单克隆抗体,以确定炎症细胞亚群的数量和分布。皮肤炎症浸润由T细胞(局部CD4/CD8比值为1.05±0.7,而外周血中为1.48±0.3)、巨噬细胞以及少量B细胞、自然杀伤细胞和粒细胞组成。大多数T细胞表达激活标志物(白细胞介素-2和转铁蛋白受体,HLA-DR+),并且观察到T细胞受体γδ表达增加。使用新获得的试剂对CD4+亚群进行分析显示,辅助性T细胞(CD4+CD45RO+)与抑制/诱导亚群(CD4+CD45RA+)的比例为1.4:1。原发性感染患者(45例)和复发患者(5例)的局部免疫变量之间没有差异。在7例患者中,在特异性治疗前和治疗后1个月对活检样本进行了分析,除了真皮CD1a+(朗格汉斯)细胞每平方毫米略有增加外,未显示出显著差异。观察到的皮肤细胞浸润模式表明,除了直接的寄生虫作用外,还存在免疫介导的组织损伤,包括T细胞介导的细胞毒性和迟发型超敏反应。