TLR Agonist Therapy of Metastatic Breast Cancer in Mice.

IF 3.2 4区 医学 Q3 IMMUNOLOGY
Dennis M Klinman, Emilie Goguet, Debra Tross
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引用次数: 0

Abstract

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.

Abstract Image

Abstract Image

Abstract Image

TLR激动剂治疗小鼠转移性乳腺癌。
toll样受体(TLR) 7/8和9激动剂刺激先天免疫反应,支持肿瘤特异性免疫的发展。先前的研究表明,这两种激动剂单独使用都可以治愈小鼠的小肿瘤,当它们联合使用时,它们可以阻止较大肿瘤(>300 mm 3)的进展。为了检验这些药物联合使用是否能控制转移性疾病,我们用高侵袭性66cl4三阴性乳腺肿瘤细胞系刺激同基因小鼠。通过荧光素酶标记的肿瘤细胞的生物发光成像证实,直到肺部转移确定后才开始治疗。结果表明,TLR7/8和TLR9激动剂联合治疗原发性和转移性肿瘤,可显著降低肿瘤负担,延长生存期。环磷酰胺和抗pd - l1的加入使肿瘤得到最佳控制,其特点是平均生存时间增加了5倍。
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来源期刊
Journal of Immunotherapy
Journal of Immunotherapy 医学-免疫学
CiteScore
6.90
自引率
0.00%
发文量
79
审稿时长
6-12 weeks
期刊介绍: Journal of Immunotherapy features rapid publication of articles on immunomodulators, lymphokines, antibodies, cells, and cell products in cancer biology and therapy. Laboratory and preclinical studies, as well as investigative clinical reports, are presented. The journal emphasizes basic mechanisms and methods for the rapid transfer of technology from the laboratory to the clinic. JIT contains full-length articles, review articles, and short communications.
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