Sperling Rhoda S, Fife Kenneth H, Warren Terri J, Dix Lynn P, Brennan Clare A
Mount Sinai Medical Center, New York City, New York, USA.
Sex Transm Dis. 2008 Mar;35(3):286-90. doi: 10.1097/OLQ.0b013e31815b0132.
A substantial number of HSV-2 seropositive individuals lack a history of clinically recognized genital herpes. These individuals can transmit disease during periods of asymptomatic viral shedding. The frequency of asymptomatic shedding and the efficacy of antiviral therapy in reducing shedding has not been assessed in this population.
To compare the effect of valacyclovir 1 g once daily for 60 days versus placebo on asymptomatic viral shedding in immunocompetent, HSV-2 seropositive subjects without a history of symptomatic genital herpes infection.
Seventy-three subjects were randomized to receive valacyclovir 1 g daily or placebo for 60 days each in a 2-way crossover design. A daily swab of the genital area was self-collected for HSV-2 detection by polymerase chain reaction.
Fifty-six subjects with at least 1 polymerase chain reaction measurement in both treatment periods comprised the primary efficacy population. Valacyclovir significantly reduced shedding during subclinical days compared to placebo [mean, 1.5% vs. 5.1% of subclinical days (P <0.001), a 71% reduction]. Eighty-four percent of subjects had no shedding while receiving valacyclovir versus 54% of subjects on placebo (P <0.001). Eighty-eight percent of patients receiving valacyclovir had no recognized signs or symptoms versus 77% for placebo (P = 0.033). Valacyclovir was not associated with any safety risk compared with placebo.
In this study, asymptomatic viral shedding occurred in a substantial number of HSV-2 seropositive subjects without a history of genital herpes. Valacyclovir 1 g daily significantly reduced asymptomatic shedding compared with placebo in this population.
大量单纯疱疹病毒2型(HSV-2)血清学阳性个体并无临床确诊的生殖器疱疹病史。这些个体可在无症状病毒脱落期传播疾病。该人群中无症状病毒脱落的频率以及抗病毒治疗在减少病毒脱落方面的疗效尚未得到评估。
比较免疫功能正常、HSV-2血清学阳性且无有症状生殖器疱疹感染病史的受试者,每日服用1克伐昔洛韦持续60天与服用安慰剂相比,对无症状病毒脱落的影响。
73名受试者采用双交叉设计,随机分为两组,分别每日服用1克伐昔洛韦或安慰剂,各持续60天。受试者每日自行采集生殖器部位拭子,通过聚合酶链反应检测HSV-2。
在两个治疗期均至少进行1次聚合酶链反应检测的56名受试者构成主要疗效人群。与安慰剂相比,伐昔洛韦显著减少了亚临床期的病毒脱落[亚临床期平均病毒脱落天数,分别为1.5%和5.1%(P<0.001),减少了71%]。接受伐昔洛韦治疗的受试者中84%无病毒脱落,而接受安慰剂治疗的受试者中这一比例为54%(P<0.001)。接受伐昔洛韦治疗的患者中88%无明显体征或症状,接受安慰剂治疗的患者中这一比例为77%(P = 0.033)。与安慰剂相比,伐昔洛韦未显示出任何安全风险。
在本研究中,大量无生殖器疱疹病史的HSV-2血清学阳性受试者出现无症状病毒脱落。在该人群中,每日服用1克伐昔洛韦与安慰剂相比,显著减少了无症状病毒脱落。