淋巴毒素
溶瘤病毒
细菌
生物
淋巴毒素β受体
细胞因子
沙门氏菌
调解人
癌症研究
微生物学
受体
肠沙门氏菌
病毒
免疫学
病毒学
细胞生物学
生物化学
遗传学
作者
Markus Loeffler,Gaëlle Le'Negrate,Maryla Krajewska,John C. Reed
标识
DOI:10.1073/pnas.0701959104
摘要
Intravenously administered bacteria reportedly accumulate in tumors. Furthermore, systemic administration of attenuated Salmonella typhimurium has little or no significant side-effects in humans. Consequently, we engineered such bacteria to improve their oncolytic activity by stably inserting a gene encoding LIGHT, a cytokine known to promote tumor rejection. Unlike control bacteria, attenuated S. typhimurium expressing LIGHT inhibited growth of primary tumors, as well as the dissemination of pulmonary metastases, in various mouse tumor models employing murine carcinoma cell lines in immunocompetent mice. Antitumor activity was achieved without significant toxicity and was associated with infiltration of inflammatory cells and dependent on the LIGHT receptors, herpes virus entry mediator (HVEM), and lymphotoxin-β receptor (LTβR). These findings provide evidence that nonvirulent bacteria can be exploited as targeting vehicles for local generation of therapeutic proteins in tumors.
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