Matteucci D, Pistello M, Mazzetti P, Giannecchini S, Del Mauro D, Lonetti I, Zaccaro L, Pollera C, Specter S, Bendinelli M
Department of Biomedicine, University of Pisa, Italy.
J Virol. 1997 Nov;71(11):8368-76. doi: 10.1128/JVI.71.11.8368-8376.1997.
Cats immunized with cells infected with a primary isolate of feline immunodeficiency virus (FIV) and fixed with paraformaldehyde were challenged with cell-free or cell-associated homologous virus obtained ex vivo. Complete protection was observed in animals challenged with cell-free virus 4 months after completion of vaccination (p.v.) or with cell-associated virus 12 months p.v. In contrast, no protection was observed in cats challenged with cell-free virus 12 or 28 months p.v. or with cell-associated virus 37.5 months p.v. Prior to the 28- and 37.5-month challenges, the animals had received a booster dose of vaccine that had elicited a robust anamnestic immune response. These results show that vaccine-induced protection against ex vivo FIV is achievable but is relatively short-lived and can be difficult to boost.
用感染了猫免疫缺陷病毒(FIV)原代分离株且经多聚甲醛固定的细胞免疫的猫,接受了体外获得的无细胞或细胞相关同源病毒的攻击。在接种疫苗(p.v.)4个月后用无细胞病毒攻击的动物,或在接种疫苗12个月后用细胞相关病毒攻击的动物中观察到完全保护。相比之下,在接种疫苗12或28个月后用无细胞病毒攻击的猫,或在接种疫苗37.5个月后用细胞相关病毒攻击的猫中未观察到保护作用。在28个月和37.5个月攻击之前,这些动物接受了一剂能引发强烈回忆性免疫反应的加强疫苗。这些结果表明,疫苗诱导的针对体外FIV的保护是可以实现的,但相对短暂且难以加强。