Department of Pediatrics, Interdepartmental Program in Immunology, and Institute for Immunity, Transplantation, and Infection, Stanford University, Stanford, California 94305, USA.
J Virol. 2010 Dec;84(24):12691-702. doi: 10.1128/JVI.00769-10. Epub 2010 Oct 13.
Influenza A virus is a negative-strand segmented RNA virus in which antigenically distinct viral subtypes are defined by the hemagglutinin (HA) and neuraminidase (NA) major viral surface proteins. An ideal inactivated vaccine for influenza A virus would induce not only highly robust strain-specific humoral and T-cell immune responses but also cross-protective immunity in which an immune response to antigens from a particular viral subtype (e.g., H3N2) would protect against other viral subtypes (e.g., H1N1). Cross-protective immunity would help limit outbreaks from newly emerging antigenically novel strains. Here, we show in mice that the addition of cationic lipid/noncoding DNA complexes (CLDC) as adjuvant to whole inactivated influenza A virus vaccine induces significantly more robust adaptive immune responses both in quantity and quality than aluminum hydroxide (alum), which is currently the most widely used adjuvant in clinical human vaccination. CLDC-adjuvanted vaccine induced higher total influenza virus-specific IgG, particularly for the IgG2a/c subclass. Higher levels of multicytokine-producing influenza virus-specific CD4 and CD8 T cells were induced by CLDC-adjuvanted vaccine than with alum-adjuvanted vaccine. Importantly, CLDC-adjuvanted vaccine provided significant cross-protection from either a sublethal or lethal influenza A viral challenge with a different subtype than that used for vaccination. This superior cross-protection afforded by the CLDC adjuvant required CD8 T-cell recognition of viral peptides presented by classical major histocompatibility complex class I proteins. Together, these results suggest that CLDC has particular promise for vaccine strategies in which T cells play an important role and may offer new opportunities for more effective control of human influenza epidemics and pandemics by inactivated influenza virus vaccine.
甲型流感病毒是一种负链分段 RNA 病毒,其抗原上不同的病毒亚型由血凝素(HA)和神经氨酸酶(NA)这两种主要的病毒表面蛋白来定义。一种理想的甲型流感病毒灭活疫苗不仅要能诱导出高度强健的、针对特定毒株的体液免疫和 T 细胞免疫应答,还要能诱导出交叉保护免疫应答,即针对某种特定病毒亚型(如 H3N2)的免疫应答能够保护机体免受其他病毒亚型(如 H1N1)的感染。交叉保护免疫应答有助于限制新出现的、抗原性全新的病毒株引起的暴发。在这里,我们在小鼠中证明,阳离子脂质/非编码 DNA 复合物(CLDC)作为佐剂添加到全灭活流感病毒疫苗中,能够比目前在临床人类疫苗接种中应用最广泛的佐剂——氢氧化铝(alum)更显著地诱导出数量和质量上更加强健的适应性免疫应答。CLDC 佐剂疫苗诱导出更高水平的针对流感病毒的总 IgG,特别是 IgG2a/c 亚类。与 alum 佐剂疫苗相比,CLDC 佐剂疫苗诱导出更高水平的产生多种细胞因子的针对流感病毒的 CD4 和 CD8 T 细胞。重要的是,CLDC 佐剂疫苗提供了针对与用于疫苗接种的病毒亚型不同的、亚致死或致死性的甲型流感病毒攻击的显著交叉保护。CLDC 佐剂所赋予的这种优越的交叉保护作用需要 CD8 T 细胞识别由经典主要组织相容性复合体 I 类蛋白呈递的病毒肽。总之,这些结果表明,CLDC 在 T 细胞发挥重要作用的疫苗策略中具有特别的应用前景,它可能为通过灭活流感病毒疫苗更有效地控制人类流感流行和大流行提供新的机会。