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Updated: Aug 8, 2026

Generation of Human CD40-activated B cells
Published on: October 17, 2009
CD40 ligand-positive CD8+ T cell clones allow B cell growth and differentiation
P Hermann1, C Van-Kooten, C Gaillard
1Schering-Plough, Laboratory for Immunological Research, Dardilly, France.
Insights
Activated CD8+ T cells expressing CD40 ligand (CD40L) can stimulate B cell growth and differentiation. This CD40L-CD40 interaction is crucial for T cell-dependent B cell responses, with varying effects based on CD40L expression levels.
Area of Science:
- Immunology
- Cell Biology
Background:
- Activated CD8+ T cells can express CD40 ligand (CD40L), a molecule vital for T cell-dependent B cell stimulation.
- The role of CD8+ T cell CD40L expression in B cell activation and differentiation requires further elucidation.
Purpose of the Study:
- To investigate the capacity of CD8+ T cell clones with varying CD40L expression levels to promote B cell growth and differentiation.
- To determine the dependence of T cell-mediated B cell activation on the CD40-CD40L interaction.
Main Methods:
- Analysis of CD40L expression on activated CD8+ T cell clones.
- Co-culture of B cells with different CD8+ T cell clones.
- Assessment of B cell proliferation and immunoglobulin production.
- Use of blocking monoclonal antibodies against CD40L and CD40.
- Flow cytometry analysis of B cell activation markers (CD25, CD80, CD86).
Main Results:
- CD8+ T cell clones were categorized into high, intermediate, and low CD40L-expressing subsets.
- High and intermediate CD40L-expressing CD8+ T cell clones, with IL-2 and IL-10, induced significant B cell proliferation and immunoglobulin production.
- B cell responses were partially neutralized by anti-CD40L and anti-CD40 antibodies, indicating a CD40L-CD40-dependent mechanism.
- All CD8+ T cell clone types upregulated B cell activation markers.
Conclusions:
- CD8+ T cells can drive B cell growth and differentiation in a CD40L-CD40-dependent manner.
- The level of CD40L expression on CD8+ T cells correlates with their ability to stimulate B cells.
- CD40-CD40L interaction is a significant, but not exclusive, pathway for CD8+ T cell-mediated B cell activation.
Abstract:
A fraction of activated CD8+ T cells expresses CD40 ligand (CD40L), a molecule that plays a key role in T cell-dependent B cell stimulation. CD8+ T cell clones were examined for CD40L expression and for their capacity to allow the growth and differentiation of B cells, upon activation with immobilized anti-CD3. According to CD40L expression, CD8+ clones could be grouped into three subsets. CD8+ T cell clones expressing high levels of CD40L (> or = 80% CD40L+ cells) were equivalent to CD4+ T cell clones with regard to induction of tonsil B cell proliferation and immunoglobulin (Ig) production, provided the combination of interleukin (IL)-2 and IL-10 was added to cultures. CD8+ T cell clones, with intermediate levels of CD40L expression (10 to 30% CD40L+ cells), also stimulated B cell proliferation and Ig secretion with IL-2 and IL-10. B cell responses induced by these CD8+ T cell clones were neutralized by blocking monoclonal antibodies specific for either CD40L or CD40. By contrast, CD40L- T cell clones (< or = 5% CD40L+ cells), only induced marginal B cell responses even with IL-2 and IL-10. All three clone types were able to activate B cells as shown by up-regulation of CD25, CD80 and CD86 expression. A neutralizing anti-CD40L antibody indicated that T cell-dependent B cell activation was only partly dependent on CD40-CD40L interaction. These CD40L- clones had no inhibitory effects on B cell proliferation induced by CD40L-expressing CD8+ T cell clones. Taken together, these results indicate that CD8+ T cells can induce B cell growth and differentiation in a CD40L-CD40-dependent fashion.
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