Harbour D A, Gunn-Moore D A, Gruffydd-Jones T J, Caney S M A, Bradshaw J, Jarrett O, Wiseman A
Department of Clinical Veterinary Science, Division of Molecular and Cellular Biology, University of Bristol, Langford House, Langford, Bristol BS40 5DU, UK.
Vaccine. 2002 Jul 26;20(23-24):2866-72. doi: 10.1016/s0264-410x(02)00237-2.
The duration of immunity provided by a feline leukemia virus (FeLV) vaccine, Leukocell 2, was determined. Kittens were vaccinated when 9 and 12 weeks of age and were challenged 12 months later with FeLV-A/Glasgow-1. An oronasal challenge protocol without corticosteroid enhancement was developed in order to induce a persistent viraemia in a high proportion of adult cats. Fourteen of 18 (80%) of the vaccinated cats challenged in this way remained non-viraemic while 9/15 (60%) of age-matched controls became persistently infected, a preventable fraction of 63%. This difference was statistically significant (P=0.038). For comparison, 10 of 12 (83%) 15-17-week-old kittens challenged in the same way became persistently infected, confirming the relative resistance of adult animals to FeLV. Tests for virus neutralising and anti-feline oncornavirus-associated cell membrane antigen (FOCMA) antibodies suggested that the former were more important than the latter in protection. Thus, Leukocell 2 protected a significant proportion of cats from FeLV challenge 1 year after primary vaccination as kittens.
确定了猫白血病病毒(FeLV)疫苗Leukocell 2所提供的免疫持续时间。小猫在9周龄和12周龄时接种疫苗,并在12个月后用FeLV-A/格拉斯哥-1进行攻毒。为了在高比例的成年猫中诱导持续性病毒血症,制定了一种不使用皮质类固醇增强的口鼻攻毒方案。以这种方式攻毒的18只接种疫苗的猫中有14只(80%)仍无病毒血症,而年龄匹配的对照组中有9/15(60%)被持续感染,可预防比例为63%。这种差异具有统计学意义(P=0.038)。作为比较,以同样方式攻毒的12只15 - 17周龄小猫中有10只(83%)被持续感染,证实了成年动物对FeLV的相对抗性。病毒中和试验和抗猫肿瘤病毒相关细胞膜抗原(FOCMA)抗体检测表明,前者在保护中比后者更重要。因此,Leukocell 2在小猫初次接种疫苗1年后保护了相当比例的猫免受FeLV攻毒。