Pollock R V, Carmichael L E
Am J Vet Res. 1983 Feb;44(2):169-75.
Modified live feline panleukopenia virus (FPLV) vaccine protected dogs against canine parvovirus (CPV) infection. However, unlike the long-lived (greater than or equal to 20-month) immunity engendered by CPV infection, the response of dogs to living FPLV was variable. Doses of FPLV (snow leopard strain) in excess of 10(5.7) TCID50 were necessary for uniform immunization; smaller inocula resulted in decreased success rates. The duration of immunity, as measured by the persistence of hemagglutination-inhibiting antibody, was related to the magnitude of the initial response to vaccination; dogs with vigorous initial responses resisted oronasal CPV challenge exposure 6 months after vaccination, and hemagglutination-inhibiting antibodies persisted in such dogs for greater than 1 year. Limited replication of FPLV in dogs was demonstrated, but unlike CPV, the feline virus did not spread to contact dogs or cats. Adverse reactions were not associated with living FPLV vaccination, and FPLV did not interfere with simultaneous response to attenuated canine distemper virus.
改良活猫泛白细胞减少症病毒(FPLV)疫苗可保护犬类免受犬细小病毒(CPV)感染。然而,与CPV感染产生的长期(大于或等于20个月)免疫力不同,犬类对活FPLV的反应是可变的。为实现均匀免疫,FPLV(雪豹毒株)的剂量超过10(5.7) TCID50是必要的;较小的接种量会导致成功率降低。通过血凝抑制抗体的持续存在来衡量的免疫持续时间,与疫苗接种初始反应的强度相关;初始反应强烈的犬在接种疫苗6个月后能抵抗口鼻CPV攻击暴露,且此类犬的血凝抑制抗体持续存在超过1年。已证明FPLV在犬体内有有限复制,但与CPV不同,猫病毒不会传播给接触的犬或猫。不良反应与活FPLV疫苗接种无关,且FPLV不干扰对减毒犬瘟热病毒的同时反应。