Reuter Jon D, Vivas-Gonzalez Beatriz E, Gomez Daniel, Wilson Jean H, Brandsma Janet L, Greenstone Heather L, Rose John K, Roberts Anjeanette
Section of Comparative Medicine, Yale University School of Medicine, New Haven, Connecticut 06510, USA.
J Virol. 2002 Sep;76(17):8900-9. doi: 10.1128/jvi.76.17.8900-8909.2002.
Immunizations with live recombinant vesicular stomatitis viruses (rVSV) expressing foreign viral proteins have successfully protected animals from challenges with several heterologous viruses. We developed an rVSV expressing the major capsid protein (L1) of cottontail rabbit papillomavirus (CRPV) and tested the efficacy of protection following CRPV challenge. An rVSV expressing L1 of CRPV (VSV-L1) was characterized for the protective ability afforded by intranasal, intradermal, or intramuscular vaccination in rabbits subsequently challenged with CRPV. Protein expression of L1 in VSV-L1 was confirmed by radioimmunoprecipitation assays. Nuclear localization of L1 was demonstrated by indirect immunofluorescence assays. Immunized rabbits elicited significant VSV neutralization and VLP-L1 enzyme-linked immunosorbent assay titers. VSV-L1 vaccination was not associated with weight loss or any other adverse clinical signs in the rabbit model. VSV shedding in nasal secretions occurred in some rabbits, peaking at 4 to 6 days after intranasal vaccination, with no further shedding after day 6. Specific humoral immunity to the L1 protein was consistently seen after a single VSV-L1 vaccination when administered through an intradermal or intramuscular route or after a boost via the intranasal route. Rabbits were completely protected from CRPV-induced papillomas after VSV-L1 vaccination and boost given intranasally or intramuscularly. Vaccination with VSV-L1 is a novel approach to prevent papillomavirus-induced disease and demonstrates a potential strategy for developing a human papillomavirus vaccine that can be given without injection.
用表达外源病毒蛋白的重组水泡性口炎病毒(rVSV)进行免疫接种已成功保护动物免受多种异源病毒的攻击。我们构建了一种表达棉尾兔乳头瘤病毒(CRPV)主要衣壳蛋白(L1)的rVSV,并测试了CRPV攻击后其保护效果。对表达CRPV的L1的rVSV(VSV-L1)进行了表征,以确定其在经鼻、皮内或肌肉注射接种兔子后,再用CRPV攻击时所提供的保护能力。通过放射免疫沉淀试验确认了VSV-L1中L1的蛋白表达。通过间接免疫荧光试验证明了L1的核定位。免疫兔子产生了显著的VSV中和抗体和VLP-L1酶联免疫吸附试验效价。在兔模型中,VSV-L1接种与体重减轻或任何其他不良临床症状无关。一些兔子的鼻分泌物中出现了VSV脱落,在经鼻接种后4至6天达到峰值,6天后不再有脱落。当通过皮内或肌肉注射途径单次接种VSV-L1或经鼻途径加强接种后,始终能观察到对L1蛋白的特异性体液免疫。经鼻或肌肉注射接种VSV-L1并加强接种后,兔子完全免受CRPV诱导的乳头瘤的侵害。用VSV-L1接种是预防乳头瘤病毒引起疾病的一种新方法,并展示了开发一种无需注射的人乳头瘤病毒疫苗的潜在策略。