B Cells Regulate Macrophage Phenotype and Response to Chemotherapy in Squamous Carcinomas

被引:285
作者
Affara, Nesrine I. [1 ]
Ruffell, Brian [1 ,5 ,8 ]
Medler, Terry R. [5 ]
Gunderson, Andrew J. [5 ]
Johansson, Magnus [1 ]
Bornstein, Sophia [7 ]
Bergsland, Emily [2 ,4 ]
Steinhoff, Martin [3 ]
Li, Yijin [9 ]
Gong, Qian [9 ]
Ma, Yan [9 ]
Wiesen, Jane F. [1 ,5 ]
Wong, Melissa H. [5 ,6 ,8 ]
Kulesz-Martin, Molly [5 ,6 ,8 ]
Irving, Bryan [9 ]
Coussens, Lisa M. [1 ,4 ,5 ,8 ]
机构
[1] Univ Calif San Francisco, Dept Pathol, San Francisco, CA 94143 USA
[2] Univ Calif San Francisco, Dept Med, San Francisco, CA 94143 USA
[3] Univ Calif San Francisco, Dept Dermatol, San Francisco, CA 94143 USA
[4] Univ Calif San Francisco, Helen Diller Family Comprehens Canc Ctr, San Francisco, CA 94143 USA
[5] Oregon Hlth & Sci Univ, Dept Cell & Dev Biol, Portland, OR 97239 USA
[6] Oregon Hlth & Sci Univ, Dept Dermatol, Portland, OR 97239 USA
[7] Oregon Hlth & Sci Univ, Dept Radiat Med, Portland, OR 97239 USA
[8] Oregon Hlth & Sci Univ, Knight Canc Inst, Portland, OR 97239 USA
[9] Genentech Inc, San Francisco, CA 94080 USA
关键词
HUMAN-PAPILLOMAVIRUS; MOUSE MODEL; T-CELLS; CANCER; CARCINOGENESIS; IMMUNOTHERAPY; PROGRESSION; EXPRESSION; RITUXIMAB; THERAPY;
D O I
10.1016/j.ccr.2014.04.026
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
B cells foster squamous cell carcinoma (SCC) development through deposition of immunoglobulin-containing immune complexes in premalignant tissue and Fc gamma receptor-dependent activation of myeloid cells. Because human SCCs of the vulva and head and neck exhibited hallmarks of B cell infiltration, we examined B cell-deficient mice and found reduced support for SCC growth. Although ineffective as a single agent, treatment of mice bearing preexisting SCCs with B cell-depleting alpha CD20 monoclonal antibodies improved response to platinum- and Taxol-based chemotherapy. Improved chemoresponsiveness was dependent on altered chemokine expression by macrophages that promoted tumor infiltration of activated CD8(+) lymphocytes via CCR5-dependent mechanisms. These data reveal that B cells, and the downstream myeloid-based pathways they regulate, represent tractable targets for anticancer therapy in select tumors.
引用
收藏
页码:809 / 821
页数:13
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