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Pharmacokinetics and Pharmacodynamics in HIV Prevention; Current Status and Future Directions: A Summary of the DAIDS and BMGF Sponsored Think Tank on Pharmacokinetics (PK)/Pharmacodynamics (PD) in HIV Prevention

机译:预防艾滋病毒的药代动力学和药效学;现状和未来方向:DAIDS和BMGF赞助的关于预防HIV的药代动力学(PK)/药效学(PD)的智囊团的摘要

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摘要

Thirty years after its beginning, the HIV/AIDS epidemic is still raging around the world. According to UNAIDS, in 2011 alone 1.7M deaths were attributable to AIDS, and 2.5M people were newly infected by the virus. Despite the success in treating HIV-infected people with potent antiretroviral drugs, preventing HIV infection is the key to ending the epidemic. Recently, the efficacy of topical and systemic antiviral chemoprophylaxis (i.e., preexposure prophylaxis or “PrEP”), using the same drugs used for HIV treatment, has been demonstrated in a number of clinical trials. However, results from other trials have been inconsistent, especially those evaluating PrEP in women. These inconsistencies may result from our incomplete understanding of pharmacokinetics (PK)/pharmacodynamics (PD) at the mucosal sites of sexual transmission: the male and female gastrointestinal and reproductive tracts. The drug concentrations used in these trials were derived from those used for treatment; however, we still do not know the relationship between the therapeutic and the preventive dose. This article presents the first comprehensive review of the available data in the HIV pharmacology field from animal models to human studies, and outlines gaps, challenges, and future directions. Addressing these pharmacological gaps and challenges will be critical in selecting and advancing future PrEP candidates and strategies with the greatest impact on the HIV epidemic.
机译:自开始流行三十年以来,艾滋病毒/艾滋病的流行仍在全世界蔓延。根据联合国艾滋病规划署的数据,仅2011年就有170万人死于艾滋病,而250万人是新感染该病毒的人。尽管使用有效的抗逆转录病毒药物成功治疗了艾滋病毒感染者,但预防艾滋病毒感染仍是结束这一流行病的关键。最近,在许多临床试验中已经证明了使用与HIV治疗相同的药物进行局部和全身性抗病毒化学预防(即暴露前预防或“ PrEP”)的功效。但是,其他试验的结果却不一致,尤其是那些评估女性PrEP的试验。这些不一致可能是由于我们对性传播的粘膜部位(男性和女性胃肠道和生殖道)的药代动力学(PK)/药效学(PD)的不完全了解所致。这些试验中使用的药物浓度来自用于治疗的药物浓度;但是,我们仍然不知道治疗剂量和预防剂量之间的关系。本文将对从动物模型到人体研究的HIV药理学领域的可用数据进行首次全面综述,并概述差距,挑战和未来方向。解决这些药理学差距和挑战对于选择和推进对HIV流行病影响最大的未来PrEP候选人和策略至关重要。

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