Streck H, Bogdan C, Tingle A, Röllinghoff M
Zentralbl Bakteriol Mikrobiol Hyg A. 1987 Mar;263(4):594-604. doi: 10.1016/s0176-6724(87)80204-3.
A comparison has been made between the capacity of macrophages of BALB/c "non-healer" mice and C57BL/6 "healer" mice to deal in vitro with Leishmania tropica (L. tropica) parasites in order to obtain a more detailed picture of the inherent contribution of macrophages to the susceptibility of BALB/c mice to infection with L. tropica and the resulting fatal course of the disease. In comparison to macrophages of C57BL/6 origin, BALB/c macrophages showed a higher parasite uptake and a higher infection rate; they allowed a more rapid transformation of L. tropica promastigotes into amastigotes and displayed less leishmanicidal activities. Lymphokine-rich culture supernatants induced activation of macrophages resulting in killing of L. tropica by macrophages of both, "non-healer" and "healer" mice. These supernatants also induced expression of Ia-antigens on infected "non-healer" and "healer" macrophages. The results of this study clearly point to the critical role of macrophage functions to either support a systemic leishmaniasis or to alternatively mount a protective immune response leading to a self-healing course of the disease.
为了更详细地了解巨噬细胞对BALB/c小鼠感染热带利什曼原虫(L. tropica)易感性及由此导致的致命病程的内在作用,对BALB/c“非治愈型”小鼠和C57BL/6“治愈型”小鼠的巨噬细胞在体外处理热带利什曼原虫的能力进行了比较。与C57BL/6来源的巨噬细胞相比,BALB/c巨噬细胞表现出更高的寄生虫摄取率和感染率;它们能使热带利什曼原虫前鞭毛体更快地转化为无鞭毛体,且杀利什曼原虫活性较低。富含淋巴因子的培养上清液可诱导巨噬细胞活化,导致“非治愈型”和“治愈型”小鼠的巨噬细胞均能杀死热带利什曼原虫。这些上清液还可诱导受感染的“非治愈型”和“治愈型”巨噬细胞表达Ia抗原。本研究结果清楚地表明,巨噬细胞功能对于支持全身性利什曼病或引发导致疾病自愈的保护性免疫反应起着关键作用。