Immunogenicity of Unadjuvanted and AF03-Adjuvanted A/H1N1/California/07/2009 Influenza Vaccines in Naïve and Influenza-Primed Mice

Fabienne Piras , Catherine Caillet , Marie-Clotilde Bernard , Aymeric De Monfort , Frederick R. Vogel , Inca C. Kusters
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Abstract

Influenza A virus of swine origin caused the first pandemic of the 21st century. In accordance with WHO recommendations, pandemic influenza vaccines were manufactured using the A/California/07/2009 (H1N1) strain and these vaccines were first evaluated in preclinical studies.

We evaluated the immunogenicity of the A/California/07/2009 (H1N1) vaccine in both naïve and influenza-primed mice. Animals were intramuscularly-immunized on D0 and D21 with 0.3 or 3 μg of hemagglutinin administered with or without AF03 adjuvant. Immunogenicity of the various formulations was compared to that of other seasonal H1N1 and H5N1 strains. Additionally, we investigated the impact of prior or concomitant immunization with seasonal trivalent inactivated influenza vaccine (TIV). The immune response was assessed by hemagglutination inhibition and microneutralization assays.

In naïve mice, a single dose of unadjuvanted A/H1N1/California/07/2009 vaccine elicited HI titers > 40, and a second vaccine dose strongly increased these titers. In the presence of AF03, even a low vaccine dosage elicited high antibody titers (HI titers > 700). The antibody responses induced by both unadjuvanted and adjuvanted-vaccine were similar to those induced by other seasonal H1N1 strains and were superior to those induced by H5N1 vaccine strains. In mice previously primed with TIV, the unadjuvanted pandemic (H1N1) 2009 vaccine induced higher functional antibody titers than in naïve mice. However the AF03-adjuvanted vaccine induced similar antibody titers in both naïve and primed mice. The concomitant administration of TIV together with pandemic (H1N1) 2009 vaccine did not affect antibody responses generated against A/California/07/2009 or A/Brisbane/59/2007 seasonal H1N1 strain.

The pandemic (H1N1) 2009 unadjuvanted influenza vaccine was shown to be immunogenic in mice after a single immunization. Formulation of the vaccine with AF03 adjuvant strongly increased its immunogenicity and enabledimmune response to the pandemic (H1N1) 2009 or to the H1N1 strain contained in the seasonal TIV.

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A/H1N1/California/07/2009无佐剂和af03佐剂流感疫苗在Naïve和流感引物小鼠中的免疫原性
猪源性甲型流感病毒引起了21世纪的第一次大流行。根据世卫组织的建议,使用A/California/07/2009 (H1N1)毒株生产了大流行性流感疫苗,这些疫苗首先在临床前研究中进行了评估。我们在naïve和流感引发小鼠中评估了A/California/07/2009 (H1N1)疫苗的免疫原性。分别以0.3或3 μg血凝素加或不加AF03佐剂给药于D0和D21肌内免疫。将各种制剂的免疫原性与其他季节性H1N1和H5N1毒株进行了比较。此外,我们还调查了事先或同时接种季节性三价灭活流感疫苗(TIV)的影响。免疫反应通过血凝抑制和微量中和试验进行评估。在naïve小鼠中,单剂无佐剂的a/ H1N1/California/07/2009疫苗可引起HI滴度>第二剂疫苗可显著提高这些滴度。在AF03存在的情况下,即使低剂量的疫苗也能激发出高抗体滴度(HI滴度>700)。无佐剂和加佐剂疫苗诱导的抗体应答与其他季节性H1N1毒株诱导的抗体应答相似,且优于H5N1毒株诱导的抗体应答。在先前接种过TIV的小鼠中,未加佐剂的2009年H1N1大流行疫苗诱导的功能抗体滴度高于naïve小鼠。然而,af03佐剂疫苗在naïve和引物小鼠中诱导了相似的抗体滴度。TIV与2009年H1N1流感大流行疫苗同时接种不影响针对A/California/07/2009或A/Brisbane/59/2007季节性H1N1毒株产生的抗体应答。2009年H1N1流感大流行无佐剂流感疫苗在小鼠单次免疫后显示出免疫原性。用AF03佐剂配制的疫苗可显著提高其免疫原性,增强对2009年H1N1大流行或季节性TIV中包含的H1N1毒株的免疫应答。
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