Kim Jong R, Holbrook Beth C, Hayward Sarah L, Blevins Lance K, Jorgensen Matthew J, Kock Nancy D, De Paris Kristina, D'Agostino Ralph B, Aycock S Tyler, Mizel Steven B, Parks Griffith D, Alexander-Miller Martha A
Department of Microbiology and Immunology, Wake Forest School of Medicine, Winston-Salem, North Carolina, USA.
Department of Pathology, Section of Comparative Medicine, Wake Forest School of Medicine, Winston-Salem, North Carolina, USA.
J Virol. 2015 Jul;89(14):7291-303. doi: 10.1128/JVI.00549-15. Epub 2015 May 6.
Influenza virus can cause life-threatening infections in neonates and young infants. Although vaccination is a major countermeasure against influenza, current vaccines are not approved for use in infants less than 6 months of age, in part due to the weak immune response following vaccination. Thus, there is a strong need to develop new vaccines with improved efficacy for this vulnerable population. To address this issue, we established a neonatal African green monkey (AGM) nonhuman primate model that could be used to identify effective influenza vaccine approaches for use in young infants. We assessed the ability of flagellin, a Toll-like receptor 5 (TLR5) agonist, to serve as an effective adjuvant in this at-risk population. Four- to 6-day-old AGMs were primed and boosted with inactivated PR8 influenza virus (IPR8) adjuvanted with either wild-type flagellin or inactive flagellin with a mutation at position 229 (m229), the latter of which is incapable of signaling through TLR5. Increased IgG responses were observed following a boost, as well as at early times after challenge, in infants vaccinated with flagellin-adjuvanted IPR8. Inclusion of flagellin during vaccination also resulted in a significantly increased number of influenza virus-specific T cells following challenge compared to the number in infants vaccinated with the m229 adjuvant. Finally, following challenge infants vaccinated with IPR8 plus flagellin exhibited a reduced pathology in the lungs compared to that in infants that received IPR8 plus m229. This study provides the first evidence of flagellin-mediated enhancement of vaccine responses in nonhuman primate neonates.
Young infants are particularly susceptible to severe disease as a result of influenza virus infection. Compounding this is the lack of effective vaccines for use in this vulnerable population. Here we describe a vaccine approach that results in improved immune responses and protection in young infants. Incorporation of flagellin during vaccination resulted in increased antibody and T cell responses together with reduced disease following virus infection. These results suggest that flagellin may serve as an effective adjuvant for vaccines targeted to this vulnerable population.
流感病毒可在新生儿和幼儿中引发危及生命的感染。尽管接种疫苗是预防流感的主要对策,但目前的疫苗未被批准用于6个月以下的婴儿,部分原因是接种疫苗后免疫反应较弱。因此,迫切需要为这一脆弱人群开发疗效更佳的新型疫苗。为解决这一问题,我们建立了一种新生非洲绿猴(AGM)非人灵长类动物模型,可用于确定适用于幼儿的有效流感疫苗接种方法。我们评估了鞭毛蛋白(一种Toll样受体5(TLR5)激动剂)在这一高危人群中作为有效佐剂的能力。对4至6日龄的AGM用野生型鞭毛蛋白或第229位发生突变的无活性鞭毛蛋白(m229)佐剂的灭活PR8流感病毒(IPR8)进行初次免疫和加强免疫,后者无法通过TLR5发出信号。在用鞭毛蛋白佐剂的IPR8疫苗接种的婴儿中,加强免疫后以及攻击后早期观察到IgG反应增加。与用m229佐剂接种疫苗的婴儿相比,接种疫苗期间加入鞭毛蛋白还导致攻击后流感病毒特异性T细胞数量显著增加。最后,攻击后,与接受IPR8加m229的婴儿相比,用IPR8加鞭毛蛋白接种疫苗的婴儿肺部病理变化减轻。本研究首次证明了鞭毛蛋白介导的非人灵长类新生儿疫苗反应增强。
幼儿因感染流感病毒特别容易患重病。更复杂的是,这一脆弱人群缺乏有效的疫苗。在此,我们描述了一种疫苗接种方法,可改善幼儿的免疫反应并提供保护。接种疫苗期间加入鞭毛蛋白可增加抗体和T细胞反应,并减少病毒感染后的疾病发生。这些结果表明,鞭毛蛋白可能作为针对这一脆弱人群的疫苗的有效佐剂。