Department of Virology, Umeå University, Umeå, Sweden.
Antimicrob Agents Chemother. 2012 Nov;56(11):5735-43. doi: 10.1128/AAC.01072-12. Epub 2012 Aug 20.
Herpes simplex viruses 1 and 2 (HSV-1 and HSV-2) are responsible for lifelong latent infections in humans, with periods of viral reactivation associated with recurring ulcerations in the orofacial and genital tracts. In immunosuppressed patients and neonates, HSV infections are associated with severe morbidity and, in some cases, even mortality. Today, acyclovir is the standard therapy for the management of HSV infections. However, the need for novel antiviral agents is apparent, since HSV isolates resistant to acyclovir therapy are frequently isolated in immunosuppressed patients. In this study, we assessed the anti-HSV activity of the antiadenoviral compounds 2-[2-(2-benzoylamino)-benzoylamino]benzoic acid (benzavir-1) and 2-[4,5-difluoro-2-(2-fluorobenzoylamino)-benzoylamino]benzoic acid (benzavir-2) on HSV-1 and HSV-2. Both compounds were active against both viruses. Importantly, benzavir-2 had potency similar to that of acyclovir against both HSV types, and it was active against clinical acyclovir-resistant HSV isolates.
单纯疱疹病毒 1 型和 2 型(HSV-1 和 HSV-2)可在人体中引起终身潜伏感染,病毒再激活期与口腔和生殖器部位的复发性溃疡有关。在免疫抑制患者和新生儿中,HSV 感染可导致严重发病,在某些情况下甚至导致死亡。目前,阿昔洛韦是治疗 HSV 感染的标准疗法。然而,显然需要新型抗病毒药物,因为在免疫抑制患者中经常分离到对阿昔洛韦治疗耐药的 HSV 分离株。在这项研究中,我们评估了抗腺病毒化合物 2-[2-(2-苯甲酰胺基)-苯甲酰胺基]苯甲酸(苯扎维-1)和 2-[4,5-二氟-2-(2-氟苯甲酰胺基)-苯甲酰胺基]苯甲酸(苯扎维-2)对 HSV-1 和 HSV-2 的抗 HSV 活性。这两种化合物对两种病毒均具有活性。重要的是,苯扎维-2 对两种 HSV 型的效力与阿昔洛韦相似,并且对临床阿昔洛韦耐药的 HSV 分离株有效。