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Killing of Leishmania donovani by activated liver macrophages from resistant and susceptible strains of mice.

作者信息

Olivier M, Bertrand S, Tanner C E

出版信息

Int J Parasitol. 1989 Jul;19(4):377-83. doi: 10.1016/0020-7519(89)90093-3.

DOI:10.1016/0020-7519(89)90093-3
PMID:2777460
Abstract

Leishmania donovani is an obligate intracellular protozoan parasite of macrophages; liver macrophages are, however, the only population of cells which express the resistant Lsh gene phenotype when these cells are infected in vitro. It was of interest to study in vitro the action of Con A-stimulated spleen cell lymphokines (LK) to protect or to cure liver macrophages from infection by L. donovani. Liver and peritoneal macrophages (PEC) from resistant (C57L/J) and susceptible (C57BL/6J) mice were infected in vitro with promastigotes before or after LK treatment; the percentage of infected macrophages was determined 4, 24, 48 and 72 h post-infection. Both macrophage populations were protected or cured by treatment with lymphokines; the cells of the resistant strain were protected or cured more effectively than those of the susceptible strain. The capacity for cure or for protection following LK treatment of liver and PEC macrophages was similar within each strain. Supernatants from the IL-2-produced MLA-144 cell line had no effect to protect or cure macrophages. This study indicates that the response of macrophages to the action of LK is also important in determining the susceptibility of mice to L. donovani; this model in vitro provides a good approximation of the response of macrophages to therapy.

摘要

相似文献

1
Killing of Leishmania donovani by activated liver macrophages from resistant and susceptible strains of mice.
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引用本文的文献

1
Role of inorganic nitrogen oxides and tumor necrosis factor alpha in killing Leishmania donovani amastigotes in gamma interferon-lipopolysaccharide-activated macrophages from Lshs and Lshr congenic mouse strains.无机氮氧化物和肿瘤坏死因子α在来自Lshs和Lshr同源小鼠品系的γ干扰素-脂多糖激活的巨噬细胞中杀伤杜氏利什曼原虫无鞭毛体的作用。
Infect Immun. 1991 Nov;59(11):3935-44. doi: 10.1128/iai.59.11.3935-3944.1991.