Activation of human B lymphocytes through CD40 and interleukin 4

We have produced and characterized a new CD40 monoclonal antibody, mAb 89, which in the presence of anti‐IgM antibodies co‐stimulates to induce B cell proliferation. mAb 89 activates resting B cells as shown by an increase in cell volume and an enhanced subsequent proliferation of B cells in respons...

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Veröffentlicht in:European journal of immunology 1989-08, Vol.19 (8), p.1463-1467
Hauptverfasser: Vallé, Alain, Zuber, Caroline E., Defrance, Thierry, Djossou, Odile, Riem, Menno De, Banchereau, Jacques
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Sprache:eng
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Zusammenfassung:We have produced and characterized a new CD40 monoclonal antibody, mAb 89, which in the presence of anti‐IgM antibodies co‐stimulates to induce B cell proliferation. mAb 89 activates resting B cells as shown by an increase in cell volume and an enhanced subsequent proliferation of B cells in response to anti‐IgM antibody. However, mAb 89 does not prepare B cells to respond to the growth‐promoting activity of interleukin (IL) 2 or IL4. Unlike IL 2 and IL 4, mAb 89 only weakly stimulates the proliferation of anti‐IgM pre‐activated B cells. Thus, the activating properties of anti‐CD40 are likely to explain its co‐stimulatory effect on B cells. Interestingly, the anti‐CD40 mAb 89 was found to act in synergy with IL 4, but not with IL 2, in co‐stimulation and restimulation assays. In this respect, anti‐CD40 does not induce a significant increase of B cell surface IL 4 receptors while IL 4, but not IL 2, induces a twofold increase of the CD40 antigen expression. Thus the synergistic interaction between IL 4 and anti‐CD40 may be related to the IL 4‐dependent increase of CD40 antigen expression.
ISSN:0014-2980
1521-4141
DOI:10.1002/eji.1830190818