| Literature DB >> 7681403 |
P Hermann1, D Blanchard, B de Saint-Vis, F Fossiez, C Gaillard, B Vanbervliet, F Brière, J Banchereau, J P Galizzi.
Abstract
To identify the ligand(s) of the human CD40 antigen, a cDNA encoding the extracellular domain of the CD40 antigen was fused to a cDNA encoding the constant region (Fc) of human IgG1. The CD40-Fc fusion protein was able to specifically bind to CD4+ and various CD8+ T cell clones activated with immobilized anti-CD3. The 125I-labeled CD40-Fc fusion protein bound anti-CD3 activated CD4+ T cell clone (MT9) with an equilibrium dissociation constant (Kd) of 10-20 nM. The human CD40-binding protein expressed on the cell surface of activated T lymphocytes is a monomeric protein of approximately 32 kDa. Minor components of 29 kDa and 17 kDa were also detected. A small proportion of CD4+ and CD8+ blood mononuclear T cells activated by anti-CD3 expressed the CD40 ligand but its detection was best observed following depletion of B cells. Addition of B cells to purified T cells abolished the binding of CD40-Fc obtained after anti-CD3 activation.Entities:
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Year: 1993 PMID: 7681403 DOI: 10.1002/eji.1830230430
Source DB: PubMed Journal: Eur J Immunol ISSN: 0014-2980 Impact factor: 5.532