癌症研究
趋化因子
生物
CD8型
渗透(HVAC)
髓样
头颈部鳞状细胞癌
免疫系统
B细胞
趋化因子受体
抗体
免疫学
作者
Nesrine I. Affara,Brian Ruffell,Terry R. Medler,Andrew J. Gunderson,Magnus Johansson,Sophia Bornstein,Emily K. Bergsland,Martin Steinhoff,Yijin Li,Qian Gong,Yan Ma,Jane F. Wiesen,Melissa H. Wong,Molly Kulesz-Martin,Bryan Irving,Lisa M. Coussens
出处
期刊:Cancer Cell
[Cell Press]
日期:2014-06-16
卷期号:25 (6): 809-821
被引量:203
标识
DOI:10.1016/j.ccr.2014.04.026
摘要
B cells foster squamous cell carcinoma (SCC) development through deposition of immunoglobulin-containing immune complexes in premalignant tissue and Fcγ 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 αCD20 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.
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