Manservigi R, Incorvaia C, Di Luca D, Rotola A, Balboni P G, Sebastiani A, Rossi A, Cassai E
Institute of Microbiology, University of Ferrara, Italy.
J Med Virol. 1990 Nov;32(3):148-54. doi: 10.1002/jmv.1890320304.
The efficacy of different therapies and vaccine preparations was assessed for treating or preventing herpetic ocular keratitis induced by experimental inoculation in rabbits with two HSV-1 variants that display different pathogenetic potential. Early administration of acyclovir (ACV) promoted fast healing and prevented neurologic involvements: alpha-interferon (alpha-IFN) was less efficient than ACV; combined therapy with both drugs increased the antiviral effects. In an attempt to prevent the disease, rabbits were vaccinated with a slightly pathogenic HSV-1 variant or with a secreted form of an engineered HSV-1 glycoprotein gB (gB-1s) and were subsequently challenged with a highly pathogenic HSV-1 variant. Immunization of rabbits with gB-1s was much more efficient than immunization with live virus in reducing the severity of herpetic keratitis and in preventing CNS disease.
使用两种具有不同致病潜力的单纯疱疹病毒1型(HSV-1)变体对家兔进行实验接种,以诱导疱疹性角膜结膜炎,评估了不同治疗方法和疫苗制剂治疗或预防该疾病的效果。早期给予阿昔洛韦(ACV)可促进快速愈合并预防神经受累:α干扰素(α-IFN)的效果不如ACV;两种药物联合治疗可增强抗病毒效果。为预防该疾病,给家兔接种致病性稍低的HSV-1变体或工程化HSV-1糖蛋白gB的分泌形式(gB-1s),随后用高致病性HSV-1变体进行攻击。在家兔中,用gB-1s免疫在减轻疱疹性角膜炎的严重程度和预防中枢神经系统疾病方面比用活病毒免疫更有效。