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卡氏肺孢子虫病从受感染宿主的免疫功能正常接触者传播至易感宿主。

Transmission of Pneumocystis carinii disease from immunocompetent contacts of infected hosts to susceptible hosts.

作者信息

Dumoulin A, Mazars E, Seguy N, Gargallo-Viola D, Vargas S, Cailliez J C, Aliouat E M, Wakefield A E, Dei-Cas E

机构信息

Department of Microbiology of Ecosystems, Pasteur Institute of Lille, France.

出版信息

Eur J Clin Microbiol Infect Dis. 2000 Sep;19(9):671-8. doi: 10.1007/s100960000354.

Abstract

Pneumocystis carinii organisms constitute a large group of heterogeneous atypical microscopic fungi that are able to infect immunocompromised mammals by an airborne route and to proliferate in their lungs, inducing Pneumocystis carinii pneumonia. This pneumonia remains a crucial epidemiological challenge, since neither the source of Pneumocystis carinii infection in humans nor the process by which humans become infected has been clearly established. Polymerase chain reaction (PCR) assays have shown that profoundly immunosuppressed patients without pneumocystosis can be subclinically infected with Pneumocystis. Other PCR-based studies have suggested that healthy immunocompetent hosts are not latent carriers of the parasite. However, recent reports have indicated that Pneumocystis carinii can persist for limited periods in the lungs of convalescent rats after recovery from corticosteroid-induced pneumocystosis, and also that immunocompetent mammals can be transiently parasitized by Pneumocystis carinii after close contact with hosts with Pneumocystis carinii pneumonia. Can transiently parasitized hosts be a source of infection for immunosuppressed hosts? In order to investigate this important clinical question, the ability of immunocompetent BALB/c mice, which were carrying subclinical levels of Pneumocystis carinii, to transmit the infection by the airborne route to highly susceptible, uninfected mice with severe combined immunodeficiency was studied. The results indicated that the immunocompetent mice, transiently parasitized by Pneumocystis carinii organisms after close contact with Pneumocystis carinii-infected mice, were able to transmit the infection to Pneumocystis carinii-free mice with severe combined immunodeficiency.

摘要

卡氏肺孢子虫属于一大类异质性非典型微观真菌,可通过空气传播途径感染免疫功能低下的哺乳动物,并在其肺部增殖,引发卡氏肺孢子虫肺炎。这种肺炎仍然是一个关键的流行病学挑战,因为人类卡氏肺孢子虫感染的来源以及人类感染的过程均尚未明确。聚合酶链反应(PCR)检测表明,未患肺孢子虫病的深度免疫抑制患者可能会受到卡氏肺孢子虫的亚临床感染。其他基于PCR的研究表明,健康的免疫功能正常宿主并非该寄生虫的潜伏携带者。然而,最近的报告指出,从皮质类固醇诱导的肺孢子虫病恢复后的恢复期大鼠肺部,卡氏肺孢子虫可在有限时间内持续存在,而且免疫功能正常的哺乳动物在与患有卡氏肺孢子虫肺炎的宿主密切接触后,可能会被卡氏肺孢子虫短暂寄生。短暂被寄生的宿主会成为免疫抑制宿主的感染源吗?为了研究这个重要的临床问题,研究了携带亚临床水平卡氏肺孢子虫的免疫功能正常的BALB/c小鼠通过空气传播途径将感染传播给高度易感的、未感染的严重联合免疫缺陷小鼠的能力。结果表明,与感染卡氏肺孢子虫的小鼠密切接触后被卡氏肺孢子虫短暂寄生的免疫功能正常小鼠,能够将感染传播给无卡氏肺孢子虫的严重联合免疫缺陷小鼠。

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