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夏氏疟原虫沙巴变种:低疟原虫血症对CB6F1小鼠免疫力的影响。

Plasmodium chabaudi chabaudi: effect of low parasitemias on immunity in CB6F1 mice.

作者信息

Favila-Castillo L, Monroy-Ostria A, Garcia-Tapia D

机构信息

Department of Immunology, National School of Biological Sciences, Carpio y Plan de Ayala, Colonia Santo Tomas, Mexico City, 11340, Mexico.

出版信息

Exp Parasitol. 1999 May;92(1):73-80. doi: 10.1006/expr.1999.4399.

Abstract

We examined the effect that low parasitemias have on the immune response of CB6F1 mice infected with Plasmodium chabaudi chabaudi AS. Ascending parasitemias were stopped by chloroquine treatment when they were between 1.6 and 9.4%. Mice that suffered low parasitemias developed good immunity to homologous reinfection but, contrary to what happened in mice that suffered full parasitemias, they did not develop immunity to heterologous reinfection with Plasmodium yoelii 17XL. Total IgG antiparasite antibody responses were similar in mice that suffered low or full parasitemia, both in primary infection and after reinfection. At the level of isotypes, IgM, IgG1, IgG2b, and IgG3 responses were similar in mice that suffered low or full parasitemias, but after reinfection, mice that suffered low parasitemias responded with higher levels of IgG2a than mice that suffered full parasitemias. Mice that suffered low parasitemias did not have splenomegaly but their immunity to homologous reinfection was diminished after splenectomy in a manner similar to that of splenectomized mice that suffered full parasitemia. CB6F1 mice can develop homologous immunity even if exposed to low parasitemias but cannot develop heterologous immunity unless exposed to high parasite loads.

摘要

我们研究了低疟原虫血症对感染恰氏疟原虫AS株的CB6F1小鼠免疫反应的影响。当疟原虫血症在1.6%至9.4%之间时,通过氯喹治疗阻止其上升。经历低疟原虫血症的小鼠对同源再感染产生了良好的免疫力,但与经历完全疟原虫血症的小鼠不同的是,它们对约氏疟原虫17XL的异源再感染没有产生免疫力。在初次感染和再感染后,经历低疟原虫血症或完全疟原虫血症的小鼠中,总的抗寄生虫IgG抗体反应相似。在同种型水平上,经历低疟原虫血症或完全疟原虫血症的小鼠中,IgM、IgG1、IgG2b和IgG3反应相似,但在再感染后,经历低疟原虫血症的小鼠产生的IgG2a水平高于经历完全疟原虫血症的小鼠。经历低疟原虫血症的小鼠没有脾肿大,但脾切除后它们对同源再感染的免疫力减弱,其方式与经历完全疟原虫血症的脾切除小鼠相似。CB6F1小鼠即使暴露于低疟原虫血症也能产生同源免疫力,但除非暴露于高寄生虫负荷,否则不能产生异源免疫力。

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