Cocker F M, Newby T J, Gaskell R M, Evans P A, Gaskell C J, Stokes C R, Harbour D A, Bourne J F
Res Vet Sci. 1986 Nov;41(3):323-30.
Intranasal vaccination with a cold-adapted strain of feline herpesvirus type 1 (FHV-1) two days before challenge gave partial protection, and four days before challenge gave complete protection, against feline viral rhinotracheitis. Protection at this time appeared to be specific since vaccination with FHV-1 did not affect the disease caused by the unrelated feline calicivirus. The time course of onset of protection also confirmed that the protective mechanism was likely to be specific. However, six days after vaccination only low levels of FHV-specific IgA and IgM antibody and of interferon were found in serum and nasal washings. In lymphocyte transformation assays neither peripheral blood lymphocytes nor tonsil lymphocytes gave a significant proliferative response in the presence of FHV antigen. Pathogenesis experiments demonstrated that the tonsil and nasal turbinates were the most important sites of virulent FHV-1 replication. Vaccination significantly reduced levels of infectious virus found in both sites. The results provide evidence that no one mechanism is responsible for protection following vaccination but local specific responses are more likely to be involved.
在攻毒前两天用冷适应的1型猫疱疹病毒(FHV-1)进行鼻内接种,可提供部分保护;在攻毒前四天接种,则可提供完全保护,预防猫病毒性鼻气管炎。此时的保护作用似乎具有特异性,因为用FHV-1接种不会影响由不相关的猫杯状病毒引起的疾病。保护作用开始的时间进程也证实,保护机制可能具有特异性。然而,接种疫苗六天后,在血清和鼻腔灌洗液中仅发现低水平的FHV特异性IgA和IgM抗体以及干扰素。在淋巴细胞转化试验中,外周血淋巴细胞和扁桃体淋巴细胞在FHV抗原存在的情况下均未产生显著的增殖反应。发病机制实验表明,扁桃体和鼻甲是强毒FHV-1复制的最重要部位。接种疫苗显著降低了在这两个部位发现的传染性病毒水平。结果提供了证据,表明接种疫苗后的保护作用并非由单一机制负责,而是更可能涉及局部特异性反应。