Sun J-B, Eriksson K, Li B-L, Lindblad M, Azem J, Holmgren J
Department of Medical Microbiology and Immunology, and Göteborg University Vaccine Research Institute (GUVAX), Göteborg University, S-405 30, Göteborg, Sweden.
Clin Immunol. 2004 Jul;112(1):35-44. doi: 10.1016/j.clim.2004.03.001.
We investigated the development of CD8+ tumor-specific cytotoxic lymphocytes (CTL) and protection against tumor growth after vaccination with bone marrow-derived dendritic cells (DC) pulsed with a model protein ovalbumin conjugated to cholera toxin (OVA-CT) in B6 mice using E.G7 tumor cells expressing OVA(257-264) peptide (SIINFEKL) as target cells in vitro and in vivo. Vaccination with OVA-CT-pulsed DC concurrently induced strong CTL in vitro activity and anti-E.G7 tumor protection in vivo in WT, NK-depleted and CD4-deficient mice as well as in IL-12-/- and IFN-gamma-/- mice but not in CD8-deficient mice. Importantly, activation of CTL by OVA-CT-pulsed DC was dependent on CT-induced activation of adenylate cyclase and increased cAMP production by DC associated with increased expression of MHC class I and co-stimulatory molecules (CD80, CD86 and CD40). These results show that vaccination with DC pulsed with antigens (Ag) conjugated to CT induces a strong CTL response and suggest that conjugation of tumor Ag to CT for DC vaccination represents a promising approach for tumor vaccination and immunotherapy.
我们使用表达OVA(257 - 264)肽(SIINFEKL)的E.G7肿瘤细胞作为体外和体内的靶细胞,在B6小鼠中研究了用与霍乱毒素偶联的模型蛋白卵清蛋白(OVA-CT)脉冲处理的骨髓来源树突状细胞(DC)接种疫苗后CD8 +肿瘤特异性细胞毒性淋巴细胞(CTL)的发育以及对肿瘤生长的保护作用。用OVA-CT脉冲处理的DC接种疫苗在野生型、NK细胞缺失和CD4缺陷小鼠以及IL-12基因敲除和IFN-γ基因敲除小鼠中同时诱导了体外强大的CTL活性和体内抗E.G7肿瘤保护作用,但在CD8缺陷小鼠中未诱导出这种作用。重要的是,OVA-CT脉冲处理的DC对CTL的激活依赖于CT诱导的腺苷酸环化酶激活以及DC中cAMP产生增加,这与MHC I类分子和共刺激分子(CD80、CD86和CD40)表达增加相关。这些结果表明,用与CT偶联的抗原(Ag)脉冲处理的DC接种疫苗可诱导强烈的CTL反应,并表明将肿瘤Ag与CT偶联用于DC接种疫苗是肿瘤接种疫苗和免疫治疗的一种有前景的方法。