کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
2831070 1163776 2013 11 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Manipulating mIgD-expressing B cells with anti-migis-δ monoclonal antibodies
موضوعات مرتبط
علوم زیستی و بیوفناوری بیوشیمی، ژنتیک و زیست شناسی مولکولی زیست شناسی مولکولی
پیش نمایش صفحه اول مقاله
Manipulating mIgD-expressing B cells with anti-migis-δ monoclonal antibodies
چکیده انگلیسی

Surface IgD and IgM doubly positive cells comprise the major population of B cells in the human immune system. The heavy chain of membrane-bound IgD (mδ) differs from that of IgD (δ) in that mδ contains a C-terminal membrane-anchor peptide. Our group previously proposed that the N-terminal extracellular segment of 27 aa residues of the membrane-anchor peptide of mδ, referred to as the mIg isotype-specific-δ (migis-δ) segment, may provide a unique antigenic site for isotype-specific targeting of mIgD+ B cells. Here we report the preparation of mouse mAbs specific for human migis-δ. The mAbs bound to human migis-δ-containing recombinant proteins in an ELISA and to mIgD-expressing transfectants of a CHO cell line as analyzed by flow cytometry. MAb 20E6, which binds to an epitope toward the N-terminal of human migis-δ, could stain human B cell line MC116, which expressed mIgD and mIgM. MC116 cells could be induced to undergo apoptosis by treatment with 20E6 in the presence of a second crosslinking antibody. Chimeric 20E6 caused antibody-dependent cellular cytotoxicity of MC116 cells in the presence of human PBMCs as the source of effector cells. In cultures of PBMCs, 20E6 down-regulated the population of mIgD+ B cells. The production of human IgM by transplanted MC116 cells in NOD-SCID (NOD.CB17-Prkdcscid/IcrCrlBltw) mice could be suppressed by 20E6. These results encourage further investigation of the potential of anti-migis-δ mAbs to control mIgD+ B cells, when such a manipulation may alleviate a disease state.


► An antibody that binds to membrane-bound IgD (mIgD) on B lymphocytes but not to free IgD in blood has been prepared.
► The antibody binds to the extracellular segment of the C-terminal membrane-anchor peptide of the δ heavy chain of mIgD.
► The antibody can induce apoptosis and antibody dependent cell-mediated cytotoxicity of mIgD-expressing B cells.
► The antibody can reduce the production of human IgM in the human B cell line MC116-grafted NOS-SCID mice.
► The antibody may potentially be used to target mIgD-expressing B cells, when such an effect is desired for a disease state.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Molecular Immunology - Volume 53, Issue 3, March 2013, Pages 187–197
نویسندگان
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