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伐昔洛韦对接受抗逆转录病毒治疗且既往未识别出单纯疱疹病毒2型(HSV-2)的HIV感染者体内HIV和HSV-2的影响

The effect of valacyclovir on HIV and HSV-2 in HIV-infected persons on antiretroviral therapy with previously unrecognised HSV-2.

作者信息

Van Wagoner Nicholas, Geisler William M, Bachmann Laura H, Hook Edward W

机构信息

Division of Infectious Diseases, Department of Medicine, University of Alabama at Birmingham, Birmingham, AL, USA

Division of Infectious Diseases, Department of Medicine, University of Alabama at Birmingham, Birmingham, AL, USA.

出版信息

Int J STD AIDS. 2015 Jul;26(8):574-81. doi: 10.1177/0956462414546504. Epub 2014 Aug 21.

Abstract

In the absence of antiretroviral therapy, valacyclovir may reduce HIV viral load and increase CD4+ T-lymphocyte count. We sought to evaluate the impact of valacyclovir on HIV and HSV-2 in co-infected patients receiving antiretroviral therapy with previously unrecognised HSV-2 infection. A prospective, randomised-controlled, 24-week trial of valacyclovir 1000 mg was performed. Mean CD4+ T-lymphocyte count at 24 weeks compared to baseline CD4+ T-lymphocyte count was the primary outcome. HIV viral load suppression, HSV-2 outbreaks and asymptomatic HSV-2 shedding were secondary outcomes. Participants were randomised to valacyclovir (N = 66) or placebo (N = 35). Study completion was 64%. There was no change in 24 weeks compared to baseline CD4+ T-lymphocyte count in either group (valacyclovir p = 0.91, placebo p = 0.59) or the proportion with HIV viral load suppression (valacyclovir p = 0.75, placebo p = 1.0). Genital HSV and asymptomatic HSV-2 shedding were rare. Valacyclovir had no effect on CD4+ T-lymphocyte count or HIV viral load in this population. Valacyclovir may reduce clinical outbreaks and asymptomatic HSV-2 shedding, but the rarity of these events, along with its lack of benefit on HIV, does not support its use in this clinical setting.

摘要

在未接受抗逆转录病毒治疗的情况下,伐昔洛韦可能会降低HIV病毒载量并增加CD4+ T淋巴细胞计数。我们试图评估伐昔洛韦对合并感染HIV和HSV-2且接受抗逆转录病毒治疗但之前未被识别出HSV-2感染的患者的影响。进行了一项为期24周的前瞻性、随机对照试验,使用1000毫克伐昔洛韦。24周时的平均CD4+ T淋巴细胞计数与基线CD4+ T淋巴细胞计数相比是主要结局。HIV病毒载量抑制、HSV-2发作和无症状HSV-2排毒是次要结局。参与者被随机分为伐昔洛韦组(N = 66)或安慰剂组(N = 35)。研究完成率为64%。两组中24周时与基线CD4+ T淋巴细胞计数相比均无变化(伐昔洛韦组p = 0.91,安慰剂组p = 0.59),HIV病毒载量得到抑制的比例也无变化(伐昔洛韦组p = 0.75,安慰剂组p = 1.0)。生殖器HSV发作和无症状HSV-2排毒很少见。伐昔洛韦对该人群的CD4+ T淋巴细胞计数或HIV病毒载量没有影响。伐昔洛韦可能会减少临床发作和无症状HSV-2排毒,但这些事件很少见,且对HIV无益处,因此不支持在这种临床情况下使用。

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