Koday Merika T, Leonard Jolie A, Munson Paul, Forero Adriana, Koday Michael, Bratt Debra L, Fuller James T, Murnane Robert, Qin Shulin, Reinhart Todd A, Duus Karen, Messaoudi Ilhem, Hartman Amy L, Stefano-Cole Kelly, Morrison Juliet, Katze Michael G, Fuller Deborah Heydenburg
Department of Microbiology, University of Washington, Seattle, WA, United States of America.
Washington National Primate Research Center, University of Washington, Seattle, WA, United States of America.
PLoS One. 2017 Dec 21;12(12):e0189780. doi: 10.1371/journal.pone.0189780. eCollection 2017.
Recent avian and swine-origin influenza virus outbreaks illustrate the ongoing threat of influenza pandemics. We investigated immunogenicity and protective efficacy of a multi-antigen (MA) universal influenza DNA vaccine consisting of HA, M2, and NP antigens in cynomolgus macaques. Following challenge with a heterologous pandemic H1N1 strain, vaccinated animals exhibited significantly lower viral loads and more rapid viral clearance when compared to unvaccinated controls. The MA DNA vaccine induced robust serum and mucosal antibody responses but these high antibody titers were not broadly neutralizing. In contrast, the vaccine induced broadly-reactive NP specific T cell responses that cross-reacted with the challenge virus and inversely correlated with lower viral loads and inflammation. These results demonstrate that a MA DNA vaccine that induces strong cross-reactive T cell responses can, independent of neutralizing antibody, mediate significant cross-protection in a nonhuman primate model and further supports development as an effective approach to induce broad protection against circulating and emerging influenza strains.
近期源自禽类和猪的流感病毒爆发表明流感大流行的威胁依然存在。我们研究了一种由血凝素(HA)、M2蛋白和核蛋白(NP)抗原组成的多抗原(MA)通用流感DNA疫苗在食蟹猴中的免疫原性和保护效力。在用异源大流行H1N1毒株攻击后,与未接种疫苗的对照相比,接种疫苗的动物表现出显著更低的病毒载量和更快的病毒清除速度。MA DNA疫苗诱导了强烈的血清和粘膜抗体反应,但这些高抗体滴度并无广泛中和作用。相反,该疫苗诱导了与攻击病毒发生交叉反应的具有广泛反应性的NP特异性T细胞反应,且与更低的病毒载量和炎症呈负相关。这些结果表明,一种诱导强烈交叉反应性T细胞反应的MA DNA疫苗可在不依赖中和抗体的情况下,在非人灵长类动物模型中介导显著的交叉保护作用,并进一步支持其作为一种诱导针对流行和新出现流感毒株的广泛保护的有效方法进行开发。