4.4 Article

Initiation of antiretroviral therapy leads to a rapid decline in cervical and vaginal HIV-1 shedding

期刊

AIDS
卷 21, 期 4, 页码 501-507

出版社

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1097/QAD.0b013e32801424bd

关键词

AIDS; antiretroviral therapy; cervix; female; HIV-1; vagina; virus shedding

资金

  1. FIC NIH HHS [D43 TW000007] Funding Source: Medline
  2. NIAID NIH HHS [R01 AI058698, R01 AI055343, R01-AI-055343-04, AI-58698] Funding Source: Medline

向作者/读者索取更多资源

Background: Antiretroviral therapy (ART) may decrease HIV-1 infectivity in women by reducing genital HIV-1 shedding. Objectives: To evaluate the time course and magnitude of decay in cervical and vaginal HIV-1 shedding as women initiate ART. Methods: This prospective, observational study of 20 antiretroviral-naive women initiating ART with stavudine, lamivudine, and nevirapine measured HIV-1 RNA in plasma, cervical secretions, and vaginal secretions. Qualitative polymerase chain reaction estimated HIV-1 DNA in cervical and vaginal samples. Perelson's two-phase viral decay model and non-linear random effects were used to compare RNA decay rates. Decreases in proviral DNA were evaluated using logistic regression and generalized estimating equations. Results: Significant decreases in the quantity of HIV-1 RNA were observed by day 2 in plasma (P < 0.001), day 2 in cervical secretions (P=0.001), and day 4 in vaginal secretions (P < 0.001). Modeled initial and subsequent RNA decay rates in plasma, cervical secretions, and vaginal secretions were 0.6, 0.8, and 1.2 log(10) virions/day, and 0.04, 0.05, and 0.06 log(10) virions/day, respectively. The initial decay rate for vaginal HIV-1 RNA was more rapid than for plasma RNA (P=0.02). Detection of HIV-1 DNA decreased significantly in vaginal secretions during the first week (P < 0.001). At day 28, 10 women had detectable HIV-1 RNA or proviral DNA in genital secretions. Conclusions: Genital HIV-1 shedding decreased rapidly after ART initiation, consistent with a rapid decrease in infectivity. However, incomplete viral suppression in half of these women may indicate an ongoing risk of transmission. (c) 2007 Lippincott Williams & Wilkins.

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