艾滋病毒蛋白酶抑制剂:对机会性原生动物寄生虫的影响。

Q2 Pharmacology, Toxicology and Pharmaceutics
Open Medicinal Chemistry Journal Pub Date : 2011-01-01 Epub Date: 2011-03-09 DOI:10.2174/1874104501105010040
Yenisey Alfonso, Lianet Monzote
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引用次数: 0

摘要

高活性抗逆转录病毒疗法(HAART)对艾滋病自然病史的影响延长了艾滋病毒感染者的生存期,尤其是艾滋病毒病毒载量增加的感染者。此外,抗逆转录病毒疗法还能在一定程度上预防寄生虫病。一些研究表明,在 HAART 时代,机会性寄生虫感染的发病率有所下降。尽管这些变化被归因于非核苷类逆转录酶抑制剂或艾滋病毒蛋白酶抑制剂与 HAART 中至少两种核苷类逆转录酶抑制剂联合使用所诱导的细胞介导免疫的恢复,但有证据表明,HAART 治疗下的艾滋病毒阳性患者对这些寄生虫感染的控制也是通过抑制寄生虫的蛋白酶来实现的。本综述侧重于与治疗性艾滋病毒蛋白酶抑制剂有关的现有主要数据及其对机会性原生动物寄生虫的体外和体内作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

HIV Protease Inhibitors: Effect on the Opportunistic Protozoan Parasites.

HIV Protease Inhibitors: Effect on the Opportunistic Protozoan Parasites.

HIV Protease Inhibitors: Effect on the Opportunistic Protozoan Parasites.

HIV Protease Inhibitors: Effect on the Opportunistic Protozoan Parasites.

The impact of highly active antiretroviral therapy (HAART) in the natural history of AIDS disease has been allowed to prolong the survival of people with HIV infection, particularly whose with increased HIV viral load. Additionally, the antiretroviral therapy could exert a certain degree of protection against parasitic diseases. A number of studies have been evidenced a decrease in the incidence of opportunistic parasitic infections in the era of HAART. Although these changes have been attributed to the restoration of cell-mediated immunity, induced by either non-nucleoside reverse transcriptase inhibitors or HIV protease inhibitors, in combination with at least two nucleoside reverse transcriptase inhibitors included in HAART, there are evidence that the control of these parasitic infections in HIV-positive persons under HAART, is also induced by the inhibition of the proteases of the parasites. This review focuses on the principal available data related with therapeutic HIV-protease inhibitors and their in vitro and in vivo effects on the opportunistic protozoan parasites.

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来源期刊
Open Medicinal Chemistry Journal
Open Medicinal Chemistry Journal Pharmacology, Toxicology and Pharmaceutics-Pharmaceutical Science
CiteScore
4.40
自引率
0.00%
发文量
4
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