Kaye P M
Immunology. 1987 Jul;61(3):345-9.
In order to analyse the early stages of the T-cell response to Leishmania, bioassays for detecting low levels of IL-2 receptor expression both in bulk culture and under limiting dilution conditions have been used. Infection of C57BL/10 mice with Leishmania donovani amastigotes leads to the appearance of antigen-specific T lymphocytes bearing high-affinity IL-2 receptors 24-72 hr later. Phenotypic analysis by complement-mediated cytotoxicity indicates that these activated T cells comprise both L3T4+, Lyt2- and L3T4-, Lyt2+ populations. The data also suggest the existence of activated cells bearing both these markers. By both assay techniques, the appearance of receptor-positive populations appears transitory, with few such cells detectable at 7 days post-infection. The implications of these data for further studies of murine leishmaniasis are discussed.
为了分析T细胞对利什曼原虫反应的早期阶段,已采用生物测定法在大量培养和有限稀释条件下检测低水平的白细胞介素-2受体表达。用杜氏利什曼原虫无鞭毛体感染C57BL/10小鼠,24至72小时后会出现带有高亲和力白细胞介素-2受体的抗原特异性T淋巴细胞。通过补体介导的细胞毒性进行的表型分析表明,这些活化的T细胞包括L3T4 +、Lyt2 - 和L3T4 -、Lyt2 + 群体。数据还表明存在同时带有这两种标志物的活化细胞。通过这两种测定技术,受体阳性群体的出现似乎是短暂的,感染后7天时几乎检测不到此类细胞。讨论了这些数据对进一步研究小鼠利什曼病的意义。