Sydney School of Veterinary Science, The University of Sydney, Sydney, NSW 2006, Australia.
Centre for Veterinary Education, The University of Sydney, Sydney, NSW 2006, Australia.
Viruses. 2021 Mar 12;13(3):470. doi: 10.3390/v13030470.
Although the antibody response induced by primary vaccination with Fel-O-Vax FIV (three doses, 2-4 weeks apart) is well described, the antibody response induced by annual vaccination with Fel-O-Vax FIV (single dose every 12 months after primary vaccination) and how it compares to the primary antibody response has not been studied. Residual blood samples from a primary FIV vaccination study ( = 11), and blood samples from cats given an annual FIV vaccination ( = 10), were utilized. Samples from all 21 cats were tested with a commercially available PCR assay (FIV RealPCR), an anti-p24 microsphere immunoassay (MIA), an anti-FIV transmembrane (TM; gp40) peptide ELISA, and a range of commercially available point-of-care (PoC) FIV antibody kits. PCR testing confirmed all 21 cats to be FIV-uninfected for the duration of this study. Results from MIA and ELISA testing showed that both vaccination regimes induced significant antibody responses against p24 and gp40, and both anti-p24 and anti-gp40 antibodies were variably present 12 months after FIV vaccination. The magnitude of the antibody response against both p24 and gp40 was significantly higher in the primary FIV vaccination group than in the annual FIV vaccination group. The differences in prime versus recall post-vaccinal antibody levels correlated with FIV PoC kit performance. Two FIV PoC kits that detect antibodies against gp40, namely Witness and Anigen Rapid, showed 100% specificity in cats recently administered an annual FIV vaccination, demonstrating that they can be used to accurately distinguish vaccination and infection in annually vaccinated cats. A third FIV PoC kit, SNAP Combo, had 0% specificity in annually FIV-vaccinated cats, and should not be used in any cat with a possible history of FIV vaccination. This study outlines the antibody response to inactivated Fel-O-Vax FIV whole-virus vaccine, and demonstrates how best to diagnose FIV infection in jurisdictions where FIV vaccination is practiced.
虽然 Fel-O-Vax FIV (三剂,间隔 2-4 周)初次免疫接种所引起的抗体反应已有详细描述,但每年接种 Fel-O-Vax FIV (初次免疫接种后每 12 个月接种一剂)所引起的抗体反应以及它与初次抗体反应的比较尚未研究。利用了一项初次 FIV 疫苗接种研究的残留血液样本(=11)和每年接受 FIV 疫苗接种的猫的血液样本(=10)。所有 21 只猫的样本均使用市售的 PCR 检测试剂盒(FIV RealPCR)、抗 p24 微球免疫测定(MIA)、抗 FIV 跨膜(TM;gp40)肽 ELISA 以及一系列市售的即时护理(PoC)FIV 抗体试剂盒进行了检测。PCR 检测证实,在本研究期间,所有 21 只猫均未感染 FIV。MIA 和 ELISA 检测结果表明,两种疫苗接种方案均诱导了针对 p24 和 gp40 的显著抗体反应,并且在 FIV 疫苗接种后 12 个月时,抗 p24 和抗 gp40 抗体均不同程度地存在。针对 p24 和 gp40 的抗体反应的幅度在初次 FIV 疫苗接种组中明显高于在每年 FIV 疫苗接种组中。在初次疫苗接种后与回忆性疫苗接种后抗体水平的差异与 FIV PoC 试剂盒的性能相关。两种检测 gp40 抗体的 FIV PoC 试剂盒,即 Witness 和 Anigen Rapid,在最近接受年度 FIV 疫苗接种的猫中显示出 100%的特异性,表明它们可用于准确区分年度接种的猫中的疫苗接种和感染。第三种 FIV PoC 试剂盒,SNAP Combo,在每年接种 FIV 的猫中特异性为 0%,并且不应在任何可能有 FIV 接种史的猫中使用。本研究概述了对灭活的 Fel-O-Vax FIV 全病毒疫苗的抗体反应,并展示了在实施 FIV 疫苗接种的司法管辖区中如何最好地诊断 FIV 感染。