Immature neutrophils mediate tumor cell killing via IgA but not IgG Fc receptors

被引:120
作者
Otten, MA
Rudolph, E
Dechant, M
Tuk, CW
Reijmers, RM
Beelen, RHJ
van de Winkel, JGJ
van Egmond, M
机构
[1] Vrije Univ Amsterdam Med Ctr, Dept Mol Cell Biol & Immunol, NL-1081 BT Amsterdam, Netherlands
[2] Vrije Univ Amsterdam Med Ctr, Dept Surg Oncol, NL-1081 BT Amsterdam, Netherlands
[3] Univ Utrecht, Med Ctr, Immunotherapy Lab, Dept Immunol, Utrecht, Netherlands
[4] Genmab, Utrecht, Netherlands
[5] Univ Hosp Schleswig Holstein, Div Nephrol, Kiel, Germany
关键词
D O I
10.4049/jimmunol.174.9.5472
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Antitumor Abs are promising therapeutics for cancer. Currently, most Ab-based therapies focus on IgG Ab, which interact with IgG FcR (Fc gamma R) on effector cells. In this study, we examined human and mouse neutrophil-mediated tumor cell lysis via targeting the IgA FcR, Fc alpha RI (CD89), in more detail. Fc alpha RI was the most effective FcR in triggering tumor cell killing, and initiated enhanced migration of neutrophils into tumor colonies. Importantly, immature neutrophils that are mobilized from the bone marrow upon G-CSF treatment efficiently triggered tumor cell lysis via FcaRI, but proved incapable of initiating tumor cell killing via Fc gamma R. This may provide a rationale for the disappointing results observed in some earlier clinical trials in which patients were treated with G-CSF and antitumor Ab-targeting Fc gamma R.
引用
收藏
页码:5472 / 5480
页数:9
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