Gerber J D, Ingersoll J D, Gast A M, Christianson K K, Selzer N L, Landon R M, Pfeiffer N E, Sharpee R L, Beckenhauer W H
SmithKline Beecham Animal Health, Lincoln, NE 68501.
Vaccine. 1990 Dec;8(6):536-42. doi: 10.1016/0264-410x(90)90004-6.
Cats vaccinated intranasally (i.n.) with a temperature sensitive feline infectious peritonitis virus (ts-FIPV) vaccine were protected against an FIP-inducing challenge. Seventeen of 20 vaccinated cats (85%) survived a rigorous virulent FIPV challenge that caused FIP in 12 of 12 non-vaccinated cats (100%), 10 (83%) of which died. Intranasal vaccination stimulated serum IgG and serum and salivary IgA antibody responses (measured by ELISA), FIPV-neutralizing antibody (VN), and a cell-mediated immune (CMI) response as measured by lymphocyte proliferation. The serum antibody response to vaccination was not associated with protection. In fact, the IgG, IgA and VN titres were much higher in control cats than in vaccinated cats following challenge suggesting an immune-mediated pathogenesis. In contrast, stimulation of a mucosal IgA response to vaccination was related to protection. The in vitro proliferation of peripheral blood lymphocytes in response to virulent FIPV was observed in vaccinated cats, in vaccinated and challenged cats but not in non-vaccinated challenged cats.
经鼻内(i.n.)接种温度敏感型猫传染性腹膜炎病毒(ts-FIPV)疫苗的猫对诱导FIP的攻击具有抵抗力。20只接种疫苗的猫中有17只(85%)在严格的强毒FIPV攻击中存活下来,而12只未接种疫苗的猫中有12只(100%)发生了FIP,其中10只(83%)死亡。鼻内接种疫苗刺激了血清IgG以及血清和唾液IgA抗体反应(通过ELISA测量)、FIPV中和抗体(VN)以及通过淋巴细胞增殖测量的细胞介导免疫(CMI)反应。接种疫苗后的血清抗体反应与保护作用无关。事实上,攻击后对照猫的IgG、IgA和VN滴度比接种疫苗的猫高得多,提示存在免疫介导的发病机制。相比之下,接种疫苗后黏膜IgA反应的刺激与保护作用有关。在接种疫苗的猫、接种疫苗并受到攻击的猫中观察到外周血淋巴细胞对强毒FIPV的体外增殖,而在未接种疫苗并受到攻击的猫中未观察到。