Nishikawa Hiroyoshi, Sato Eiichi, Briones Gabriel, Chen Li-Mei, Matsuo Mitsutoshi, Nagata Yasuhiro, Ritter Gerd, Jäger Elke, Nomura Hideki, Kondo Shigeto, Tawara Isao, Kato Takuma, Shiku Hiroshi, Old Lloyd J, Galán Jorge E, Gnjatic Sacha
Ludwig Institute for Cancer Research, Memorial Sloan-Kettering Cancer Center, New York, New York 10021, and Section of Microbial Pathogenesis, Yale University School of Medicine, New Haven, Connecticut 06536, USA.
J Clin Invest. 2006 Jul;116(7):1946-54. doi: 10.1172/JCI28045. Epub 2006 Jun 22.
Bacterial vectors may offer many advantages over other antigen delivery systems for cancer vaccines. We engineered a Salmonella typhimurium vaccine strain to deliver the NY-ESO-1 tumor antigen (S. typhimurium-NY-ESO-1) through a type III protein secretion system. The S. typhimurium-NY-ESO-1 construct elicited NY-ESO-1-specific CD8+ and CD4+ T cells from peripheral blood lymphocytes of cancer patients in vitro. Oral administration of S. typhimurium-NY-ESO-1 to mice resulted in the regression of established NY-ESO-1-expressing tumors. Intratumoral inoculation of S. typhimurium-NY-ESO-1 to NY-ESO-1-negative tumors resulted in delivery of antigen in vivo and led to tumor regression in the presence of preexisting NY-ESO-1-specific CD8+ T cells. Specific T cell responses against at least 2 unrelated tumor antigens not contained in the vaccine were observed, demonstrating epitope spreading. We propose that antigen delivery through the S. typhimurium type III secretion system is a promising novel strategy for cancer vaccine development.
与其他用于癌症疫苗的抗原递送系统相比,细菌载体可能具有许多优势。我们构建了一种鼠伤寒沙门氏菌疫苗菌株,通过III型蛋白分泌系统递送NY-ESO-1肿瘤抗原(鼠伤寒沙门氏菌-NY-ESO-1)。鼠伤寒沙门氏菌-NY-ESO-1构建体在体外从癌症患者的外周血淋巴细胞中诱导出NY-ESO-1特异性CD8⁺和CD4⁺T细胞。给小鼠口服鼠伤寒沙门氏菌-NY-ESO-1可使已形成的表达NY-ESO-1的肿瘤消退。将鼠伤寒沙门氏菌-NY-ESO-1瘤内接种到NY-ESO-1阴性肿瘤中,可在体内递送抗原,并在预先存在NY-ESO-1特异性CD8⁺T细胞的情况下导致肿瘤消退。观察到针对疫苗中未包含的至少2种不相关肿瘤抗原的特异性T细胞反应,证明了表位扩展。我们认为,通过鼠伤寒沙门氏菌III型分泌系统递送抗原是一种有前景的癌症疫苗开发新策略。