医学
兴奋剂
环磷酰胺
转移性乳腺癌
TLR9型
原发性肿瘤
癌症研究
转移
癌症
免疫疗法
内科学
化疗
免疫系统
乳腺癌
肿瘤科
免疫学
受体
生物
生物化学
基因
基因表达
DNA甲基化
作者
Dennis M. Klinman,Emilie Goguet,Debra Tross
标识
DOI:10.1097/cji.0000000000000467
摘要
Toll-like receptor (TLR) 7/8 and 9 agonists stimulate an innate immune response that supports the development of tumor-specific immunity. Previous studies showed that either agonist individually could cure mice of small tumors and that when used in combination, they could prevent the progression of larger tumors (>300 mm 3 ). To examine whether these agents combined could control metastatic disease, syngeneic mice were challenged with the highly aggressive 66cl4 triple-negative breast tumor cell line. Treatment was not initiated until pulmonary metastases were established, as verified by bioluminescent imaging of luciferase-tagged tumor cells. Results show that combined therapy with TLR7/8 and TLR9 agonists delivered to both primary and metastatic tumor sites significantly reduced tumor burden and extended survival. The inclusion of cyclophosphamide and anti-PD-L1 resulted in optimal tumor control, characterized by a 5-fold increase in the average duration of survival.
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