Does pregnancy affect the early response to cART?

被引:5
|
作者
Rachas, Antoine [1 ]
Warszawski, Josiane [1 ,2 ,3 ]
Le Chenadec, Jerome [1 ]
Legeai, Camille [1 ]
Teglas, Jean-Paul [1 ]
Goujard, Cecile [1 ,2 ,4 ]
Rouzioux, Christine [5 ]
Mandelbrot, Laurent [1 ,6 ,7 ]
Tubiana, Roland [8 ]
Meyer, Laurence [1 ,2 ,3 ]
机构
[1] INSERM, Ctr Res Epidemiol & Populat Hlth, U1018, Epidemiol HIV & STI Team, F-94275 Le Kremlin Bicetre, France
[2] Univ Paris 11, Paris, France
[3] Bicetre Hosp, Assistance Publ Hop Paris, Dept Publ Hlth, Paris, France
[4] Bicetre Hosp, Assistance Publ Hop Paris, Dept Internal Med, Paris, France
[5] Paris Descartes Univ, Assistance Publ Hop Paris, Hosp Necker Enfants Malad, Dept Virol, Paris, France
[6] Hosp Louis Mourier, Assistance Publ Hop Paris, Dept Obstet & Gynaecol, Colombes, France
[7] Univ Paris Diderot, Paris, France
[8] Hosp Pitie Salpetriere, Assistance Publ Hop Paris, Dept Infect & Trop Dis, Inserm U943, Paris, France
关键词
HIV; pregnancy; prevention of mother-to-child transmission; response to cART; treatment duration; TO-CHILD TRANSMISSION; ANTIRETROVIRAL TREATMENT; VIRAL LOAD; UNITED-KINGDOM; EXPOSURE; THERAPY; WOMEN; PHARMACOKINETICS; ADHERENCE; DELIVERY;
D O I
10.1097/QAD.0b013e32835ac8bc
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Objective: A part of women starting antiretroviral therapy during pregnancy fail to attain undetectable viral load by delivery. Here we studied whether pregnancy affects the early immunovirological response to combined antiretroviral therapy (cART), taking into account treatment duration and baseline characteristics. Design: Antiretroviral-naive women initiating cART since 2004 and followed in three French ANRS multicenter HIV cohorts (French Perinatal Cohort, PRIMO and COPANA). Methods: The early virological response (at 1, 3 and 6 months) and immunological increase after cART initiation were compared between women starting cART during (n = 708) and outside (n = 110) pregnancy. Relative risks were estimated in multivariate models adjusted for treatment duration, baseline viral load and CD4, sociodemographic factors and chronic hepatitis B. CD4 increases were compared by using mixed models. Results: Only 63.8% of treated pregnant women attained a viral load less than 50 copies/ml by delivery. Similarly to nonpregnant women, nearly 90% of pregnant women reached a viral load less than 400 copies/ml at M3 [adjusted RR: 1.0 (95% confidence interval 0.7-1.4)], and nearly 100% at M6 following cART initiation [0.9 (0.4-1.9)]. viral load less than 50 copies/ml was attained by 61.5% of pregnant versus 67.9% of nonpregnant women at M3 (P = 0.26), and by 82.1 versus 87.0% at M6 (P = 0.48). CD4 recovery (both number and percentage) was similar in pregnant and nonpregnant women. Results were similar for the subset of women starting a boosted protease inhibitor-containing cART. Conclusion: Pregnancy does not affect the virological response to cART below 400 copies/ml, or CD4 increase. The main reason for pregnant women not achieving viral load less than 50 copies/ml at delivery appears to be a short duration of treatment. (C) 2013 Wolters Kluwer Health vertical bar Lippincott Williams & Wilkins AIDS 2013, 27:357-367
引用
收藏
页码:357 / 367
页数:11
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