Center for Vaccine Research, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.
Infect Immun. 2014 May;82(5):2098-105. doi: 10.1128/IAI.01498-14. Epub 2014 Mar 10.
Francisella tularensis, a Gram-negative bacterium, is the causative agent of tularemia. No licensed vaccine is currently available for protection against tularemia, although an attenuated strain, dubbed the live vaccine strain (LVS), is given to at-risk laboratory personnel as an investigational new drug (IND). In an effort to develop a vaccine that offers better protection, recombinant attenuated derivatives of a virulent type A strain, SCHU S4, were evaluated in New Zealand White (NZW) rabbits. Rabbits vaccinated via scarification with the three attenuated derivatives (SCHU S4 ΔguaBA, ΔaroD, and ΔfipB strains) or with LVS developed a mild fever, but no weight loss was detected. Twenty-one days after vaccination, all vaccinated rabbits were seropositive for IgG to F. tularensis lipopolysaccharide (LPS). Thirty days after vaccination, all rabbits were challenged with aerosolized SCHU S4 at doses ranging from 50 to 500 50% lethal doses (LD50). All rabbits developed fevers and weight loss after challenge, but the severity was greater for mock-vaccinated rabbits. The ΔguaBA and ΔaroD SCHU S4 derivatives provided partial protection against death (27 to 36%) and a prolonged time to death compared to results for the mock-vaccinated group. In contrast, LVS and the ΔfipB strain both prolonged the time to death, but there were no survivors from the challenge. This is the first demonstration of vaccine efficacy against aerosol challenge with virulent type A F. tularensis in a species other than a rodent since the original work with LVS in the 1960s. The ΔguaBA and ΔaroD SCHU S4 derivatives warrant further evaluation and consideration as potential vaccines for tularemia and for identification of immunological correlates of protection.
土拉弗朗西斯菌是一种革兰氏阴性细菌,是兔热病的病原体。目前尚无针对兔热病的许可疫苗,尽管一种减毒菌株,称为活疫苗株(LVS),作为一种研究性新药(IND)用于有风险的实验室人员。为了开发提供更好保护的疫苗,评估了一种强毒 A 型菌株 SCHU S4 的重组减毒衍生物在新西兰白兔中的作用。通过划痕接种三种减毒衍生物(SCHU S4ΔguaBA、ΔaroD 和ΔfipB 菌株)或 LVS 接种的兔子出现轻度发热,但未发现体重减轻。接种后 21 天,所有接种疫苗的兔子均针对土拉弗朗西斯菌脂多糖(LPS)产生 IgG 血清阳性。接种后 30 天,所有兔子均用气溶胶化的 SCHU S4 进行攻毒,剂量范围为 50 至 500 个 50%致死剂量(LD50)。所有兔子在攻毒后均出现发热和体重减轻,但与模拟接种组相比,Mock 接种组的兔子更为严重。与模拟接种组相比,SCHU S4ΔguaBA 和ΔaroD 衍生株提供了部分保护,可降低死亡率(27%至 36%)并延长死亡时间。相比之下,LVS 和ΔfipB 株均延长了死亡时间,但无幸存者。自 20 世纪 60 年代以来,这是 LVS 在非啮齿动物物种中首次针对强毒 A 型土拉弗朗西斯菌气溶胶攻毒进行疫苗效力的证明。SCHU S4ΔguaBA 和ΔaroD 衍生株值得进一步评估和考虑,作为兔热病的潜在疫苗,并确定保护的免疫学相关性。