Titus R G, Kelso A, Louis J A
Clin Exp Immunol. 1984 Jan;55(1):157-65.
Supernatants (SN) from cloned T cell lines, lymphokine secreting tumour cell lines and mixed lymphocyte culture were analysed for their ability to induce murine peritoneal exudate cell (PEC) macrophages (M phi) parasitized with Leishmania tropica to destroy the parasite. The ability of the SN to induce parasite destruction in parasitized PEC M phi correlated with their content of macrophage activating factor/interferon. Neither granulocyte-macrophage colony stimulating factor, M phi colony stimulating factor nor interleukin 2 was required for the induction of parasiticidal activity by infected PEC M phi. Similar results were also obtained using either a different Leishmania species, Leishmania enriettii, or a second source of cells: bone marrow derived macrophages.
对克隆的T细胞系、分泌淋巴因子的肿瘤细胞系以及混合淋巴细胞培养物的上清液(SN)进行分析,以检测其诱导感染热带利什曼原虫的小鼠腹腔渗出细胞(PEC)巨噬细胞(M phi)破坏该寄生虫的能力。SN诱导寄生性PEC M phi破坏寄生虫的能力与其巨噬细胞激活因子/干扰素的含量相关。感染的PEC M phi诱导杀寄生虫活性不需要粒细胞-巨噬细胞集落刺激因子、M phi集落刺激因子或白细胞介素2。使用另一种利什曼原虫物种恩氏利什曼原虫或第二种细胞来源:骨髓来源的巨噬细胞,也获得了类似的结果。