Department of Microbiology and Immunology, The University of Texas Medical Branch at Galveston, 301 University Blvd., Room 4.142B MRB, Galveston, TX 77555-1019, USA.
Vaccine. 2013 Oct 9;31(43):4988-94. doi: 10.1016/j.vaccine.2013.08.003. Epub 2013 Aug 27.
The safety and immunogenicity of an authentic recombinant (ar) of the live, attenuated MP-12 Rift Valley fever (RVF) vaccine virus with a large deletion of the NSm gene in the pre-Gn region of the M RNA segment (arMP-12ΔNSm21/384) was tested in 4-6 month old Bos taurus calves. Phase I of this study evaluated the neutralizing antibody response, measured by 80% plaque reduction neutralization (PRNT80), and clinical response of calves to doses of 1 × 10(1) through 1 × 10(7) plaque forming units (PFU) administered subcutaneously (s.c.). Phase II evaluated the clinical and neutralizing antibody response of calves inoculated s.c. or intramuscularly (i.m.) with 1 × 10(3), 1 × 10(4) or 1 × 10(5)PFU of arMP-12ΔNSm21/384. No significant adverse clinical events were observed in the animals in these studies. Of all specimens tested, only one vaccine viral isolate was recovered and that virus retained the introduced deletion. In the Phase I study, there was no statistically significant difference in the PRNT80 response between the dosage groups though the difference in IgG response between the 1 × 10(1)PFU group and the 1 × 10(5)PFU group was statistically significant (p<0.05). The PRNT80 response of the respective dosage groups corresponded to dose of vaccine with the 1 × 10(1)PFU dose group showing the least response. The Phase II study also showed no statistically significant difference in PRNT80 response between the dosage groups though the difference in RVFV-specific IgG values was significantly increased (p<0.001) in animals inoculated i.m. with 1 × 10(4) or 1 × 10(5)PFU versus those inoculated s.c. with 1 × 10(3) or 1 × 10(5)PFU. Although the study groups were small, these data suggest that 1 × 10(4) or 1 × 10(5)PFU of arMP-12ΔNSm21/384 administered i.m. to calves will consistently stimulate a presumably protective PRNT80 response for at least 91 days post inoculation. Further studies of arMP-12ΔNSm21/384 are warranted to explore its suitability as an efficacious livestock vaccine.
安全性和免疫原性的一个真实的重组(AR)的活,减毒 MP-12 裂谷热(RVF)疫苗病毒与一个大的删除的 NSm 基因的前-Gn 区的 M RNA 段(ARMP-12ΔNSm21/384)进行了测试 4-6 个月大的牛犊。第一阶段的研究评估中和抗体反应,通过 80%斑块减少中和(PRNT80),和临床反应的小牛剂量的 1 × 10(1)通过 1 × 10(7)斑块形成单位(PFU)皮下给药(皮下)。第二阶段评估临床和中和抗体反应的小牛接种皮下或肌肉内(肌内)与 1 × 10(3),1 × 10(4)或 1 × 10(5)PFU 的 arMP-12ΔNSm21/384。没有明显的不良临床事件被观察到的动物在这些研究。所有的标本进行了测试,只有一个疫苗病毒分离株被回收和病毒保留了引入的删除。在第一阶段的研究,没有统计学意义的差异,在 PRNT80 反应之间的剂量组,虽然在 IgG 反应之间的差异 1 × 10(1)PFU 组和 1 × 10(5)PFU 组有统计学意义(P<0.05)。PRNT80 反应的相应剂量组对应的疫苗剂量与 1 × 10(1)PFU 组显示最小的反应。第二阶段的研究也没有统计学意义的差异,在 PRNT80 反应之间的剂量组,虽然差异的 RVFV-特异性 IgG 值明显增加(P<0.001)在动物接种肌内 1 × 10(4)或 1 × 10(5)PFU 与那些皮下接种 1 × 10(3)或 1 × 10(5)PFU。尽管研究小组规模较小,这些数据表明 1 × 10(4)或 1 × 10(5)PFU 的 arMP-12ΔNSm21/384 接种肌内小牛将始终刺激一个假定的保护 PRNT80 反应至少 91 天接种后。进一步的研究 arMP-12ΔNSm21/384 是有必要探讨其作为一种有效的牲畜疫苗的适用性。