Kim Min-Chul, Lee Yu-Na, Hwang Hye Suk, Lee Young-Tae, Ko Eun-Ju, Jung Yu-Jin, Cho Min Kyoung, Kim Yu-Jin, Lee Jong Seok, Ha Suk-Hoon, Kang Sang-Moo
Center for Inflammation, Immunity & Infection, Institute for Biomedical Sciences, Georgia State University, Atlanta, GA 30303, USA; Animal and Plant Quarantine Agency, Anyang City, Gyeonggi-do, Korea.
Center for Inflammation, Immunity & Infection, Institute for Biomedical Sciences, Georgia State University, Atlanta, GA 30303, USA.
Vaccine. 2014 Oct 7;32(44):5824-31. doi: 10.1016/j.vaccine.2014.08.030. Epub 2014 Aug 27.
Immunity in humans with annual vaccination does not provide effective protection against antigenically distinct strains. As an approach to improve cross-protection in the presence of pre-existing strain-specific immunity, we investigated the efficacy of heterologous and heterosubtypic protection in previously vaccinated mice at earlier times after subsequent immunization with conserved-antigenic target influenza M2 ectodomain (M2e) virus-like particle vaccine (M2e5× VLP). Immunization of mice with H1N1 split vaccine induced virus specific antibodies to homologous influenza virus but did not provide heterosubtypic hemagglutination inhibiting antibody responses and cross-protection. However, subsequent M2e5× VLP immunization induced an M2e specific antibody response as well as interferon-γ (IFN-γ) producing cells in systemic and mucosal sites. Upon lethal challenge with H3N2 or H5N1 subtype influenza viruses, subsequently immunized mice with M2e5× VLP were well protected against heterosubtypic influenza viruses. These results provide evidence that non-seasonal immunization with M2e5× VLP, an experimental candidate for universal vaccine, is a promising approach for broadening the cross-protection even in the presence of strain-specific immunity.
每年接种疫苗的人类免疫力并不能有效抵御抗原性不同的毒株。作为在已有毒株特异性免疫的情况下提高交叉保护的一种方法,我们研究了在用保守抗原靶点流感M2外膜区(M2e)病毒样颗粒疫苗(M2e5×VLP)进行后续免疫后的早期,先前接种过疫苗的小鼠中异源和异亚型保护的效果。用H1N1裂解疫苗免疫小鼠可诱导针对同源流感病毒的病毒特异性抗体,但不能提供异亚型血凝抑制抗体反应和交叉保护。然而,随后的M2e5×VLP免疫诱导了M2e特异性抗体反应以及全身和黏膜部位产生干扰素-γ(IFN-γ)的细胞。在用H3N2或H5N1亚型流感病毒进行致死性攻击后,随后用M2e5×VLP免疫的小鼠对异亚型流感病毒具有良好的保护作用。这些结果证明,作为通用疫苗的实验候选物,用M2e5×VLP进行非季节性免疫是一种有前景的方法,即使在存在毒株特异性免疫的情况下也能拓宽交叉保护。