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Updated: Aug 11, 2026

Generation of Human CD40-activated B cells
Published on: October 17, 2009
Role of CD40 antigen and interleukin-2 in T cell-dependent human B lymphocyte growth
D Blanchard1, C Gaillard, P Hermann
1Schering-Plough, Laboratory for Immunological Research, Dardilly, France.
Insights
CD40 ligand-CD40 interaction is crucial for T cell-dependent B cell responses, particularly those mediated by IL-2. However, some B cell activation, especially sIgD+ cells, may not require this specific pathway.
Area of Science:
- Immunology
- Cell Biology
Background:
- T cell-dependent B cell responses are vital for adaptive immunity.
- The role of CD40 ligand (CD40L)-CD40 interaction in these responses requires further elucidation.
Purpose of the Study:
- To investigate the specific role of CD40L-CD40 interaction in T cell-mediated B cell activation and immunoglobulin (Ig) secretion.
- To determine the influence of B cell subsets, like sIgD+ cells, in this interaction.
Main Methods:
- Purified B lymphocytes were co-cultured with irradiated, activated CD4+ T cells.
- The effect of anti-CD40 monoclonal antibody (mAb) 89 on B cell proliferation and Ig secretion was assessed.
- Differential responses of B cell subsets (sIgD+ vs. sIgD-) were analyzed.
Main Results:
- Anti-CD40 mAb 89 significantly inhibited proliferation and Ig secretion in tonsil B cells.
- Proliferation of surface (s)IgD+ B cells was less sensitive to anti-CD40 inhibition compared to sIgD- B cells.
- T cell-activated B cells showed preferential response to IL-2, contrasting with the IL-4 and IL-10 dependence in the CD40 system.
Conclusions:
- CD40L-CD40 interaction is important for IL-2 mediated T cell-dependent B cell responses.
- A subset of sIgD+ B cells might be activated independently of the CD40L-CD40 pathway.
Abstract:
In the present study, we examined the participation of CD40 ligand (L)-CD40 interaction in T cell-dependent B cell responses. To this end, purified B lymphocytes were cultured over irradiated CD4+ cloned T cells activated with immobilized anti-CD3 antibody. The anti-CD40 mAb 89 strongly blocked, in a specific fashion, both proliferation and Ig secretion of tonsil B cells. Interestingly, proliferation of surface (s)IgD+ B cell was significantly less inhibited by anti-CD40 than that of sIgD- cells. Preactivated T cells induced B cells to grow and secrete immunoglobulins preferentially in response to IL-2. This contrasts with the CD40 system where B cells are essentially responsive to IL-4 and IL-10 but not to IL-2 alone. Collectively, these data indicate that CD40L-CD40 interaction plays an important role in IL-2 mediated T cell-dependent B cell responses. However, the activation of a subset of sIgD+ cells may be independent of this interaction.
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