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卡氏肺孢子虫:我们目前处于什么状况?

Pneumocystis carinii: where are we now?

作者信息

Watson John

机构信息

Brighton Hospitals NHS Trust, Lawson Unit, Eastern Road, Brighton, UK.

出版信息

J HIV Ther. 2002 Feb;7(1):8-12.

Abstract

Pneumocystis carinii pneumonia (PCP) is still the commonest AIDS-defining condition in the UK, although absolute numbers have fallen since 1990 with the advent of prophylaxis and highly active antiretroviral therapy (HAART). Further decreases in its incidence are unlikely unless efforts are made to reduce late first presentations of HIV, improve retention of patients in care and improve adherence to P. carinii prophylaxis. The widespread development of key mutations in the P. carinii dihydropteroate synthase gene in the 1990's suggests that the organism is evolving under positive evolutionary pressure, possibly mediated by widespread use of co-trimoxazole and dapsone prophylaxis. It is not clear whether these mutants lead to treatment failure with co-trimoxazole, since most episodes are treated successfully and failure of prophylaxis is rare. Molecular diagnosis of PCP is restricted to research use, due to difficulties with sensitivity, specificity and turn-around times. Patients are infected with multiple P. carinii subtypes and re-infection from an environmental source is probably more important than re-activation of an existing infection. Person-to-person transmission does not appear to be a major source of infection in HIV-infected patients. Recent reports have highlighted the potential complications of initiating HAART during treatment of PCP.

摘要

卡氏肺孢子虫肺炎(PCP)仍是英国最常见的艾滋病界定疾病,尽管自1990年预防性治疗和高效抗逆转录病毒疗法(HAART)出现以来,其绝对病例数已有所下降。除非努力减少HIV首次就诊过晚的情况、提高患者在治疗中的留存率以及提高对卡氏肺孢子虫预防性治疗的依从性,否则其发病率不太可能进一步下降。20世纪90年代卡氏肺孢子虫二氢蝶酸合酶基因关键突变的广泛出现表明,该病原体正在正向进化压力下发生进化,这可能是由广泛使用复方新诺明和氨苯砜预防性治疗介导的。目前尚不清楚这些突变体是否会导致复方新诺明治疗失败,因为大多数病例治疗成功,预防性治疗失败很少见。由于在敏感性、特异性和周转时间方面存在困难,PCP的分子诊断仅限于研究用途。患者感染多种卡氏肺孢子虫亚型,环境源的再次感染可能比现有感染的重新激活更为重要。在HIV感染患者中,人传人似乎不是主要感染源。最近的报告强调了在PCP治疗期间启动HAART的潜在并发症。

引用本文的文献

1
Pneumocystis carinii activates the NF-kappaB signaling pathway in alveolar epithelial cells.
Infect Immun. 2005 May;73(5):2766-77. doi: 10.1128/IAI.73.5.2766-2777.2005.

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