Fc gamma RII on human B cells can mediate enhanced antigen presentation

被引:23
作者
Liu, CL
Gosselin, EJ
Guyre, PM
机构
[1] DARTMOUTH COLL SCH MED,DEPT PHYSIOL,LEBANON,NH 03756
[2] ALBANY MED COLL,DEPT MICROBIOL MOLEC GENET & IMMUNOL,ALBANY,NY 12208
关键词
D O I
10.1006/cimm.1996.0026
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The ability of Fc gamma R on monocytes and macrophages to enhance presentation of Ab-bound Ag has been well established. In contrast, studies suggest that Fc gamma RII on B cells functions primarily to suppress B cell responses. We found that presentation of tetanus toroid (TT) by human EBV-transformed B cells was enhanced by 100- to 1000-fold, when TT was targeted to Fc gamma RII on B cells by using a conjugate consisting of TT covalently linked to anti-human Fc gamma RII mAb 41H16. This enhanced presentation could be blocked by mAb 41H16, heat-aggregated human IgG, or anti-MHC Class II mAb. Similarly, multimeric immune complexes composed of rr and anti-TT mAb, SA13, and 9F12 also enhanced presentation of TT. Furthermore, Fc gamma RII on purified human peripheral blood B cells could also enhance Ag presentation. These studies provide the first clear evidence that Fc gamma RII can participate in enhanced Ag presentation by human B cells, and suggest that Fc gamma RII has the potential to play a stimulatory role in human B cell responses to Ag-Ab complexes. (C) 1996 Academic Press, Inc.
引用
收藏
页码:188 / 194
页数:7
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