南美锥虫病和艾滋病毒双重感染:实验性免疫抑制下两种南美锥虫菌株的基因分析。

Célia M Marques De Brito, Marize Q Pires, Raquel S Pacheco
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引用次数: 0

摘要

背景:最近,在感染艾滋病毒的患者中发现了恰加斯病免疫病理的新方面,并报道了与寄生虫再活化有关的异常临床表现,如皮肤病变、中枢神经系统受累和/或严重的心脏病变。为了评估免疫抑制对寄生虫遗传多样性的影响,我们对之前从合并感染艾滋病毒的慢性南美锥虫病患者体内分离出的两株未克隆的克鲁斯锥虫菌株进行了研究。结果:我们利用一个实验模型来确定免疫抑制后是否会出现基因不同的种群,这是体内选择还是体外繁殖的结果。在体外和体内条件下,我们研究了被选择的种群。第一个菌株是从一个南美锥虫病再活化病例中分离出来的,该病例的患者有四个脑部病变。结果表明,该患者至少感染了三种不同的 T. cruzi 群体。在小鼠体内经过免疫抑制后恢复的群体在遗传学上与原发性人类分离株不同。第二个菌株是从一名血友病患者/艾滋病毒阳性患者身上分离出来的,该患者有恰加斯病的心脏表现,在实验性免疫抑制后没有发现明显的基因差异。结论:患者的免疫状况、是否与感染再活化有关以及寄生虫的菌株可能在疾病过程中起着重要作用。寄生虫基因变异的体内机制或应激条件下的选择参与还需要进一步研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Chagas disease and HIV co-infection: genetic analyses of two Trypanosoma cruzi strains under experimental immunosuppression.

Chagas disease and HIV co-infection: genetic analyses of two Trypanosoma cruzi strains under experimental immunosuppression.

Chagas disease and HIV co-infection: genetic analyses of two Trypanosoma cruzi strains under experimental immunosuppression.

Chagas disease and HIV co-infection: genetic analyses of two Trypanosoma cruzi strains under experimental immunosuppression.

BACKGROUND: Recently new aspects of the immunopathology of Chagas disease have been described in patients infected with HIV and unusual clinical manifestations such as cutaneous lesions, involvement of central nervous system and/or serious cardiac lesions related to the reactivation of the parasite have been reported. Two uncloned Trypanosoma cruzi strains previously isolated from chronic chagasic patients with HIV co-infection were studied in order to evaluate the impact of the immunosuppression on the genetic diversity of the parasite. RESULTS: We have exploited an experimental model to determine whether genetically distinct populations appear after immunosuppression as a consequence of in vivo selection or in vitro propagation. The in vitro and in vivo conditions have allowed us to study the selected populations. The first strain was isolated from a case of reactivation of Chagas disease in a patient which presented four cerebral lesions. It was possible to demonstrate that the patient was infected with at least three distinct populations of T. cruzi. The population, recovered after immunosuppression, in mice was genetically divergent from the primary human isolate. The second strain, isolated from a hemophiliac/HIV positive patient presenting cardiac manifestation of Chagas disease showed no marked genetic difference after experimental immunosuppression. CONCLUSION: The immunological condition of the patient, associated or not to the reactivation of the infection, and also the strain of the parasite may have an important role during the course of the disease. The in vivo mechanism that generates parasite genetic variability or the participation of the selection under stress conditions will require further investigation.

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