淋巴因子介导的多诺瓦利什曼原虫感染和药物治疗BALB/c小鼠腹腔巨噬细胞的杀微生物活性

S Sodhi, N K Ganguly, N Malla, R C Mahajan
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引用次数: 0

摘要

在体外暴露于有丝分裂原刺激的脾脏细胞的淋巴因子(LK)后,来自未治疗小鼠的腹膜巨噬细胞对利什曼原虫和多诺瓦利什曼原虫的无毛线虫具有强效的杀微生物活性。然而,据我们所知,尚未研究已感染/治疗动物的多诺瓦氏乳杆菌感染的腹膜巨噬细胞对LK的反应。因此,在本研究中,我们研究了LK对BALB/c小鼠感染巨噬细胞后特异性感染和随后抗己糖酸钠治疗的影响。随着感染的进展,可以注意到杀微生物活性百分比的下降。还尝试在感染后的不同天数对动物进行治疗,并在体外对其进行再感染。晚期治疗组在感染后第14天和第21天均未发生体外感染。然而,感染后7天(早期治疗)获得的巨噬细胞可以在体外感染。然而,只有50%的细胞被感染。当细胞暴露于LK 72小时时,这种感染被消除。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Lymphokine mediated microbicidal activity of peritoneal macrophages from Leishmania donovani infected and drug treated BALB/c mice.

The resident peritoneal macrophages from untreated mice develop potent microbicidal activity against amastigotes of Leishmania major and Leishmania donovani after in vitro exposure to lymphokines (LK) from mitogen stimulated spleen cells. However, to the best of our knowledge, the response of L. donovani infected peritoneal macrophages from already infected/treated animals to LK has not been investigated. Therefore in the present study, the effect of LK on infected macrophages from BALB/c mice following specific infection and subsequent treatment with sodium stibogluconate has been investigated. As the infection progressed, a decrease in percent microbicidal activity was noticed. An attempt was also made to treat the animals on different post infection days and reinfect them in vitro. Infection could not be produced in vitro in late treatment groups when the treatment was given on 14 days and 21 days post infection. Whereas, macrophages obtained from animals treated on 7 days post infection (early treatment) could be infected in vitro. However, only 50% of the cells got infection. This infection was eliminated when the cells were exposed to LK for 72 hours.

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