Radiofrequency thermal ablation of breast tumors combined with intralesional administration of IL-7 and IL-15 augments anti-tumor immune responses and inhibits tumor development and metastasis

被引:56
作者
Habibi, Mehran [1 ]
Kmieciak, Maciej [1 ]
Graham, Laura [1 ]
Morales, Johanna K. [1 ]
Bear, Harry D. [1 ]
Manjili, Masoud H. [1 ]
机构
[1] Virginia Commonwealth Univ, Sch Med, Massey Canc Ctr, Dept Microbiol & Immunol, Richmond, VA 23298 USA
关键词
Radiofrequency thermal ablation (RFA); Breast cancer; Immunotherapy; Myeloid-derived suppressor cells (MDSC); Interleukin-7 (IL-7); Interleukin 15 (IL-15); CD8; T-CELLS; HEPATOCELLULAR-CARCINOMA; TRANSGENIC MICE; GM-CSF; SELECTIVE EXPRESSION; MAMMARY-CARCINOMA; IN-VIVO; CANCER; VACCINE; MODULATION;
D O I
10.1007/s10549-008-0024-3
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Tumor development or recurrence is always a matter of concern following radiofrequency thermal ablation (RFA) of tumors. To determine whether combining RFA with immunologically active cytokines might induce tumor-specific immune responses against mammary carcinoma and inhibit tumor development or metastasis, we evaluated intralesional injection of IL-7 and IL-15 in RFA-treated murine tumors. We used two different breast carcinoma models: neu-overexpressing mouse mammary carcinoma (MMC) in FVBN202 transgenic mouse and 4T1 tumors in Balb/c mouse. MMC tend to relapse even in the presence of neu-specific immune responses, and 4T1 is a weakly immunogenic, aggressive and highly metastatic transplantable tumor. In vivo growth of both of these tumors is also associated with increased numbers of CD11b+Gr1+ myeloid-derived suppressor cells (MDSC). We showed for the first time that unlike RFA alone, RFA combined with the administration of intralesional IL-7 and IL-15 (after RFA), induced immune responses to tumors, inhibited tumor development and lung metastasis, and reduced MDSC.
引用
收藏
页码:423 / 431
页数:9
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