Xiang Rong, Mizutani Noriko, Luo Yunping, Chiodoni Claudia, Zhou He, Mizutani Masato, Ba Yi, Becker Juergen C, Reisfeld Ralph A
Department of Immunology, The Scripps Research Institute, La Jolla, CA 92037, USA.
Cancer Res. 2005 Jan 15;65(2):553-61.
A novel strategy achieved the eradication of lung tumor metastases by joint suppression of angiogenesis in the tumor neovasculature and induction of tumor cell apoptosis. This was accomplished by CTLs induced by a DNA vaccine encoding secretory chemokine CCL21 and the inhibitor of apoptosis protein survivin, overexpressed by both proliferating endothelial cells in the tumor vasculature and tumor cells. Oral delivery of this DNA vaccine by doubly attenuated Salmonella typhimurium (dam(-) and AroA(-)) to such secondary lymphoid organs as Peyer's patches in the small intestine, elicited marked activation of antigen-presenting dendritic cells, and an effective CD8(+)T cell immune response against the survivin self-antigen. This resulted in eradication or suppression of pulmonary metastases of non-small cell lung carcinoma in both prophylactic and therapeutic settings in C57BL/6J mice. Moreover, the suppression of angiogenesis induced by the vaccine did not impair wound healing or fertility of treated mice. It is anticipated that such novel DNA vaccines will aid in the rational design of future strategies for the prevention and treatment of cancer.
一种新策略通过联合抑制肿瘤新生血管中的血管生成和诱导肿瘤细胞凋亡实现了肺肿瘤转移灶的根除。这是通过一种DNA疫苗诱导的细胞毒性T淋巴细胞(CTL)来完成的,该疫苗编码分泌型趋化因子CCL21和凋亡抑制蛋白survivin,肿瘤血管中增殖的内皮细胞和肿瘤细胞均过度表达这两种蛋白。通过双减毒鼠伤寒沙门氏菌(dam(-)和AroA(-))将这种DNA疫苗口服递送至小肠派氏结等二级淋巴器官,可显著激活抗原呈递树突状细胞,并引发针对survivin自身抗原的有效CD8(+)T细胞免疫反应。这导致在C57BL/6J小鼠中预防和治疗非小细胞肺癌肺转移灶时,肺转移灶得以根除或受到抑制。此外,疫苗诱导的血管生成抑制并未损害经治疗小鼠的伤口愈合或生育能力。预计此类新型DNA疫苗将有助于合理设计未来癌症预防和治疗策略。