Sodhi S, Ganguly N K, Malla N, Mahajan R C
Department of Parasitology, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
Jpn J Exp Med. 1989 Jun;59(3):103-8.
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.
来自未处理小鼠的腹腔巨噬细胞在体外暴露于丝裂原刺激的脾细胞产生的淋巴因子(LK)后,对硕大利什曼原虫和杜氏利什曼原虫的无鞭毛体产生强大的杀菌活性。然而,据我们所知,来自已感染/已治疗动物的杜氏利什曼原虫感染的腹腔巨噬细胞对LK的反应尚未得到研究。因此,在本研究中,研究了LK对BALB/c小鼠在特异性感染并随后用葡萄糖酸锑钠治疗后感染的巨噬细胞的影响。随着感染的进展,观察到杀菌活性百分比下降。还尝试在感染后的不同天数对动物进行治疗,并在体外再次感染它们。当在感染后14天和21天进行治疗时,晚期治疗组在体外无法产生感染。而从感染后7天接受治疗(早期治疗)的动物获得的巨噬细胞可以在体外被感染。然而,只有50%的细胞被感染。当细胞暴露于LK 72小时后,这种感染被消除。