Jaroskova L, Selim M M, Vlasin Z, Al-Taqui M
Parasite Immunol. 1986 Jul;8(4):381-9. doi: 10.1111/j.1365-3024.1986.tb00854.x.
The proportion of T lymphocyte populations was assessed using monoclonal antibodies (OKT3, OKT4, OKT8) and spontaneous E-rosette tests with SRBC (for total and active TE cells) in 36 patients with cutaneous leishmaniasis subdivided according to the clinical variety. The T cell profile was normal in patients with simple cutaneous leishmaniasis of early ulcerative type whereas active TE cells and OKT4 positive cells were reduced in some cases of late ulcerative type. A significant reduction of active TE cells and of OKT4 positive cells (helper/inducer phenotype) and increase of OKT8 positive cells (suppressor/cytotoxic phenotype) was observed in peripheral blood of all patients with persistent active lesions and leishmaniasis recidivans. In patients with highly ulcerated persistent lesions a low proportion of active TE cells was also demonstrated in cellular extracts from dermal tissue. The results support the data obtained in experimental leishmaniasis that lack of helper/inducer cells and generation of suppressor T cells may be responsible for the development of chronic leishmaniasis.
采用单克隆抗体(OKT3、OKT4、OKT8)以及用绵羊红细胞进行的自发E花环试验(用于检测总T细胞和活性T细胞),对36例根据临床类型进行分组的皮肤利什曼病患者的T淋巴细胞亚群比例进行了评估。早期溃疡性单纯皮肤利什曼病患者的T细胞谱正常,而在某些晚期溃疡性病例中,活性T细胞和OKT4阳性细胞减少。在所有持续性活动性病变和复发性利什曼病患者的外周血中,均观察到活性T细胞和OKT4阳性细胞(辅助/诱导表型)显著减少,以及OKT8阳性细胞(抑制/细胞毒性表型)增加。在高度溃疡的持续性病变患者的真皮组织细胞提取物中,也显示出活性T细胞比例较低。这些结果支持了在实验性利什曼病中获得的数据,即辅助/诱导细胞的缺乏和抑制性T细胞的产生可能是慢性利什曼病发展的原因。