1. Blocking the CD154–CD40 interaction with anti-CD154 antibody differentially regulates interleukin-4 synthesis in T cells and IgE production in B cells
- Author
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Koichi Ikizawa, Yukiyoshi Yanagihara, Keiichi Kajiwara, Keiji Nakagami, and Takehiro Koshio
- Subjects
CD40 ,biology ,T cell ,Interleukin ,chemical and pharmacologic phenomena ,hemic and immune systems ,inter-leukin-4 ,General Medicine ,germline Cε ,Immunoglobulin E ,Molecular biology ,medicine.anatomical_structure ,surgical procedures, operative ,biology.protein ,medicine ,Immunology and Allergy ,IgE ,CD154 ,Antibody ,CD8 ,Interleukin 4 - Abstract
Using severe combined immunodeficiency mice engrafted with peripheral blood mononuclear cells from atopic patients, we analyzed the regulatory effects of anti-CD154 antibody on the in vivo induction of human interleukin (IL)-4 and IgE expression. Although anti-CD154 treatment of engrafted mice abrogated mature Ce transcription and IgE production, IL-4 mRNA levels were enhanced by the treatment. In addition, anti-CD154-induced enhancement of intracellular IL-4 synthesis was detectable in both CD4+ and CD8+ T cell subsets. Furthermore, upregulation of germline Ce transcription could be seen in anti-CD154-treated mice. These results demonstrate that blocking the CD154-CD40 interaction with anti-CD154 differentially regulates IL-4 synthesis in T cells and IgE production in B cells. Our data also indicate that antibody ligation of CD154 on T cells causes enhanced synthesis of IL-4, thereby contributing to upregulation of germline Ce transcription in B cells.
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