Department of Infectious Diseases and Pathology, College of Veterinary Medicine, University of Florida, P.O. Box 110880, Gainesville, FL 32611, USA.
MSD Animal Health, 54-68 Ferndell Street, South-Granville, NSW 2142, Australia.
Vaccine. 2014 Feb 3;32(6):746-54. doi: 10.1016/j.vaccine.2013.05.024. Epub 2013 Jun 22.
A HIV-1 tier system has been developed to categorize the various subtype viruses based on their sensitivity to vaccine-induced neutralizing antibodies (NAbs): tier 1 with greatest sensitivity, tier 2 being moderately sensitive, and tier 3 being the least sensitive to NAbs (Mascola et al., J Virol 2005; 79:10103-7). Here, we define an FIV tier system using two related FIV dual-subtype (A+D) vaccines: the commercially available inactivated infected-cell vaccine (Fel-O-Vax(®) FIV) and its prototype vaccine solely composed of inactivated whole viruses. Both vaccines afforded combined protection rates of 100% against subtype-A tier-1 FIVPet, 89% against subtype-B tier-3 FIVFC1, 61% against recombinant subtype-A/B tier-2 FIVBang, 62% against recombinant subtype-F'/C tier-3 FIVNZ1, and 40% against subtype-A tier-2 FIVUK8 in short-duration (37-41 weeks) studies. In long-duration (76-80 weeks) studies, the commercial vaccine afforded a combined protection rate of at least 46% against the tier-2 and tier-3 viruses. Notably, protection rates observed here are far better than recently reported HIV-1 vaccine trials (Sanou et al., The Open AIDS J 2012; 6:246-60). Prototype vaccine protection against two tier-3 and one tier-2 viruses was more effective than commercial vaccine. Such protection did not correlate with the presence of vaccine-induced NAbs to challenge viruses. This is the first large-scale (228 laboratory cats) study characterizing short- and long-duration efficacies of dual-subtype FIV vaccines against heterologous subtype and recombinant viruses, as well as FIV tiers based on in vitro NAb analysis and in vivo passive-transfer studies. These studies demonstrate that not all vaccine protection is mediated by vaccine-induced NAbs.
已经建立了一个 HIV-1 分层系统,根据其对疫苗诱导的中和抗体(NAb)的敏感性将各种亚型病毒分为不同的层次:敏感性最高的为 1 层,中度敏感的为 2 层,敏感性最低的为 3 层(Mascola 等人,J Virol 2005; 79:10103-7)。在这里,我们使用两种相关的 FIV 双亚型(A+D)疫苗定义了一个 FIV 分层系统:市售的灭活感染细胞疫苗(Fel-O-Vax® FIV)及其仅由灭活全病毒组成的原型疫苗。这两种疫苗对 1 型 1 层 FIVPet 的联合保护率均为 100%,对 2 型 3 层 FIVFC1 的保护率为 89%,对重组 1 型/2 型 2 层 FIVBang 的保护率为 61%,对重组 F'/C 型 3 层 FIVNZ1 的保护率为 62%,对 2 型 2 层 FIVUK8 的保护率为 40%,这些结果均在短期(37-41 周)研究中获得。在长期(76-80 周)研究中,商业疫苗对 2 型和 3 型病毒的联合保护率至少为 46%。值得注意的是,这里观察到的保护率远远优于最近报道的 HIV-1 疫苗试验(Sanou 等人,The Open AIDS J 2012; 6:246-60)。原型疫苗对两种 3 层和一种 2 层病毒的保护作用比商业疫苗更有效。这种保护作用与疫苗诱导的针对挑战病毒的 NAb 的存在无关。这是首次对双亚型 FIV 疫苗针对异源亚型和重组病毒的短期和长期疗效进行的大规模(228 只实验室猫)研究,也是首次基于体外 NAb 分析和体内被动转移研究对 FIV 分层的研究。这些研究表明,并非所有疫苗保护都由疫苗诱导的 NAb 介导。