Stanley M A, Moore R A, Nicholls P K, Santos E B, Thomsen L, Parry N, Walcott S, Gough G
Department of Pathology, University of Cambridge, Tennis Court Road, Cambridge CB2 1QP, UK.
Vaccine. 2001 Apr 6;19(20-22):2783-92. doi: 10.1016/s0264-410x(00)00533-8.
Protection against viral challenge with canine oral papillomavirus (COPV) was achieved by immunisation via particle-mediated DNA delivery (PMDD) of a plasmid encoding the COPV L1 gene to cutaneous and oral mucosal sites in beagle dogs. The initial dose of approximately 9 microg of DNA was followed by two booster doses at 6 week intervals. A similar approach was used to vaccinate a control group of animals with plasmid DNA encoding the Hepatitis B virus S gene. Following challenge at the oral mucosa with COPV all animals vaccinated with the COPV L1 gene were protected against disease. However five of six animals in the control group developed COPV induced papillomas at the oral mucosa. Both cell-mediated lymphoproliferative and humoral antibody responses to the DNA vaccine were observed. Our data indicate that PMDD of plasmid DNA can protect against mucosal challenge with papillomavirus.
通过粒子介导的DNA传递(PMDD),将编码犬口腔乳头瘤病毒(COPV)L1基因的质粒免疫比格犬的皮肤和口腔黏膜部位,实现了对犬口腔乳头瘤病毒攻击的保护。初始剂量约为9微克DNA,随后每隔6周进行两次加强剂量。采用类似方法用编码乙肝病毒S基因的质粒DNA对一组对照动物进行免疫接种。在用COPV攻击口腔黏膜后,所有接种COPV L1基因的动物都受到了疾病保护。然而,对照组的六只动物中有五只在口腔黏膜处出现了COPV诱导的乳头瘤。观察到了对DNA疫苗的细胞介导的淋巴细胞增殖反应和体液抗体反应。我们的数据表明,质粒DNA的PMDD可以预防乳头瘤病毒的黏膜攻击。