Fine Donald L, Roberts Brian A, Teehee Max L, Terpening Sara J, Kelly Cindy L H, Raetz Janae L, Baker Dale C, Powers Ann M, Bowen Richard A
DynPort Vaccine Company LLC (DVC), A CSC Company, 64 Thomas Johnson Drive, Frederick, MD 21702, USA.
Vaccine. 2007 Feb 26;25(10):1868-76. doi: 10.1016/j.vaccine.2006.10.030. Epub 2006 Oct 27.
A new vaccine, V3526, is a live-attenuated virus derived by site-directed mutagenesis from a virulent clone of the Venezuelan equine encephalitis virus (VEEV) IA/B Trinidad donkey (TrD) strain, intended for human use in protection against Venezuelan equine encephalitis (VEE). Two studies were conducted in horses to evaluate the safety, immunogenicity, ability to boost and protective efficacy of V3526 against challenges of TrD and VEEV IE 64A99. Horses were vaccinated subcutaneously (SC) with 10(7), 10(5), 10(3) or 10(2) plaque-forming units (pfu) of V3526. Control horses were sham immunized. In the first study, challenge viruses (TrD or 64A99) were administered SC 28 days post-vaccination (PV). No viremia and only mild fluctuation in white blood cell counts were observed PV. None of the V3526 vaccinated horses showed clinical signs of disease or pathology of VEE post-challenge (PC). In contrast, control horses challenged SC with 10(4)pfu TrD became viremic and showed classical signs of VEE beginning on Day 3 PC, including elevated body temperature, anorexia, leukopenia and malaise. Moderate to severe encephalitis was found in three of five control horses challenged with TrD. Control horses challenged with 64A99 failed to develop detectable viremia, but did exhibit a brief febrile episode at 1-3 days PC. None of the 10 immunized horses challenged with 64A99 became pyrexic. Twenty four of 25 horses immunized with V3526 in the first study developed serum neutralizing antibody to TrD and 64A99 within 14 days PV. Vaccinations with V3526, at doses as low as 10(2)pfu, were safe and efficacious in protecting horses against a virulent TrD virus challenge. The second study supported that repeat dosing resulted in an increase in serum neutralizing antibody to TrD.
一种新型疫苗V3526,是一种通过定点诱变从委内瑞拉马脑炎病毒(VEEV)IA/B特立尼达驴(TrD)毒株的强毒株克隆中衍生而来的减毒活病毒,旨在用于人类预防委内瑞拉马脑炎(VEE)。在马匹中进行了两项研究,以评估V3526针对TrD和VEEV IE 64A99攻击的安全性、免疫原性、增强能力和保护效力。给马匹皮下注射10^7、10^5、10^3或10^2个空斑形成单位(pfu)的V3526。对照马进行假免疫。在第一项研究中,在接种疫苗后28天(PV)皮下注射攻击病毒(TrD或64A99)。PV期间未观察到病毒血症,白细胞计数仅有轻微波动。接种V3526的马匹在攻击后(PC)均未表现出VEE的疾病临床症状或病理变化。相比之下,用10^4 pfu TrD皮下攻击的对照马出现病毒血症,并在PC第3天开始表现出VEE的典型症状,包括体温升高、厌食、白细胞减少和不适。在五匹接受TrD攻击的对照马中,有三匹出现中度至重度脑炎。接受64A99攻击的对照马未出现可检测到的病毒血症,但在PC 1 - 3天确实出现了短暂的发热期。用64A99攻击的10匹免疫马均未发热。在第一项研究中,25匹接种V3526的马中有24匹在PV 14天内产生了针对TrD和64A99的血清中和抗体。用低至10^2 pfu剂量的V3526进行疫苗接种,在保护马匹免受强毒TrD病毒攻击方面是安全有效的。第二项研究支持重复给药会导致针对TrD的血清中和抗体增加。