Walling Dennis M, Flaitz Catherine M, Nichols C Mark
Department of Internal Medicine, Division of Infectious Diseases, University of Texas Medical Branch, Galveston 77555-0435, USA.
J Infect Dis. 2003 Sep 15;188(6):883-90. doi: 10.1086/378072. Epub 2003 Sep 3.
Nineteen cases of human immunodeficiency virus (HIV)-associated oral hairy leukoplakia (HLP) and Epstein-Barr virus (EBV) replication were treated with high-dose oral valacyclovir to inhibit productive EBV replication. The clinical, histopathological, and molecular viral responses to treatment were assessed in surgical biopsy specimens obtained before, during, and after treatment. In the majority of treated cases, HLP was resolved, and EBV replication was terminated. In many cases, the initial response to inhibition of replication was a persistent, nonproductive, EBV infection of the oral mucosa, characterized by limited expression of replicative EBV genes, especially BZLF1. In some cases, productive EBV replication recurred after discontinuation of treatment with valacyclovir. In a few treated cases, treatment failed, and productive EBV replication persisted, possibly because of the evolution of acyclovir-resistant EBV. In summary, safe treatment of HLP and of EBV replication, with valacyclovir, provides new insight into the mechanisms of EBV persistence in oral mucosa.
19例人类免疫缺陷病毒(HIV)相关的口腔毛状白斑(HLP)及爱泼斯坦-巴尔病毒(EBV)复制患者接受了高剂量口服伐昔洛韦治疗,以抑制EBV的活跃复制。在治疗前、治疗期间及治疗后获取的手术活检标本中评估了临床、组织病理学及病毒分子学对治疗的反应。在大多数接受治疗的病例中,HLP得到缓解,EBV复制终止。在许多病例中,对复制抑制的初始反应是口腔黏膜持续性、非活跃性EBV感染,其特征为复制性EBV基因(尤其是BZLF1)表达受限。在一些病例中,停用伐昔洛韦治疗后活跃的EBV复制复发。在少数接受治疗的病例中,治疗失败,活跃的EBV复制持续存在,这可能是由于对阿昔洛韦耐药的EBV进化所致。总之,使用伐昔洛韦安全治疗HLP及EBV复制,为EBV在口腔黏膜中持续存在的机制提供了新见解。