沙门氏菌 FliC d 鞭毛蛋白作为活疫苗载体或纯化蛋白对 CD8+T 细胞的佐剂效应。
CD8+ T cell adjuvant effects of Salmonella FliCd flagellin in live vaccine vectors or as purified protein.
机构信息
Department of Microbiology, Institute of Biomedical Sciences, University of São Paulo, Av. Prof. Lineu Prestes, 1374, São Paulo, SP 05008-000, Brazil.
出版信息
Vaccine. 2010 Feb 3;28(5):1373-82. doi: 10.1016/j.vaccine.2009.11.003. Epub 2009 Nov 21.
Salmonella flagellin, the flagellum structural subunit, has received particular interest as a vaccine adjuvant conferring enhanced immunogenity to soluble proteins or peptides, both for activation of antibody and cellular immune responses. In the present study, we evaluated the Salmonella enterica FliCd flagellin as a T cell vaccine adjuvant using as model the 9-mer (SYVPSAEQI) synthetic H2(d)-restricted CD8(+) T cell-specific epitope (CS(280-288)) derived from the Plasmodium yoelii circumsporozoite (CS) protein. The FliCd adjuvant effects were determined under two different conditions: (i) as recombinant flagella, expressed by orally delivered live S. Dublin vaccine strains expressing the target CS(280-288) peptide fused at the central hypervariable domain, and (ii) as purified protein in acellular vaccines in which flagellin was administered to mice either as a recombinant protein fused or admixed with the target CS(280-288) peptide. The results showed that CS(280-288)-specific cytotoxic CD8(+) T cells were primed when BALB/c mice were orally inoculated with the expressing the CS(280-288) epitope S. Dublin vaccine strain. In contrast, mice immunized with purified FliCd admixed with the CS(280-288) peptide and, to a lesser extent, fused with the target peptide developed specific cytotoxic CD8(+) T cell responses without the need of a heterologous booster immunization. The CD8(+) T cell adjuvant effects of flagellin, either fused or not with the target peptide, correlated with the in vivo activation of CD11c(+) dendritic cells. Taken together, the present results demonstrate that Salmonella flagellins are flexible adjuvant and induce adaptative immune responses when administered by different routes or vaccine formulations.
沙门氏菌鞭毛蛋白是鞭毛的结构亚单位,作为一种疫苗佐剂,它能增强可溶性蛋白或肽的免疫原性,从而激活抗体和细胞免疫反应,已引起广泛关注。在本研究中,我们使用来源于疟原虫环子孢子蛋白(CS)的 9 肽(SYVPSAEQI)作为模型,评估了沙门氏菌 enterica FliCd 鞭毛蛋白作为 T 细胞疫苗佐剂的作用。FliCd 佐剂的作用是在两种不同条件下确定的:(i)作为通过口服给予表达目标 CS(280-288)肽融合于中央高变区的活 S. Dublin 疫苗株表达的重组鞭毛蛋白,和(ii)作为在无细胞疫苗中给予小鼠的纯化蛋白,其中鞭毛蛋白以重组蛋白的形式融合或与目标 CS(280-288)肽混合给予。结果表明,当 BALB/c 小鼠口服接种表达 CS(280-288)表位的 S. Dublin 疫苗株时,CS(280-288)特异性细胞毒性 CD8(+) T 细胞被激活。相比之下,用纯化的 FliCd 与 CS(280-288)肽混合免疫的小鼠(融合程度较低),在无需异源加强免疫的情况下,会产生特异性细胞毒性 CD8(+) T 细胞反应。鞭毛蛋白(融合或不融合目标肽)的 CD8(+) T 细胞佐剂作用与体内 CD11c(+)树突状细胞的激活相关。总之,本研究结果表明,沙门氏菌鞭毛蛋白是一种灵活的佐剂,当通过不同途径或疫苗制剂给予时,能诱导适应性免疫反应。