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Updated: Aug 12, 2026

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Generation of Human CD40-activated B cells
Published on: October 17, 2009
Recombinant CD40 ligand exerts potent biologic effects on T cells
W C Fanslow1, K N Clifford, M Seaman
1Immunex Research and Development Corporation, Seattle, WA 98101.
Journal of Immunology (Baltimore, Md. : 1950)
|May 1, 1994
Summary
CD40 ligand (CD40L) activates murine T cells, enhancing their proliferation and cytokine production. This finding suggests CD40L plays a key role in T:T cell interactions and immune regulation.
Area of Science:
- Immunology
- Cell Biology
- Molecular Biology
Background:
- CD40 ligand (CD40L) is known to activate B cells, stimulating proliferation and immunoglobulin secretion.
- Previous research focused on CD40L's role in B cell function, with limited understanding of its impact on T cells.
Purpose of the Study:
- To investigate the effect of CD40L on murine T cell activation and function.
- To explore CD40L's role in T cell proliferation and the expression of activation markers.
Main Methods:
- Isolation of murine CD4+ and CD8+ T cells from lymphoid tissues.
- Culture of T cells with submitogenic doses of mitogens (Con A, PHA) or antibodies (CD3, TCR-alpha beta) in the presence or absence of CD40L.
- Analysis of T cell proliferation, interleukin-2 (IL-2) production, and expression of activation antigens (IL-2R alpha, CD69).
Main Results:
- CD40L induced proliferation in both CD4+ and CD8+ T cells when co-cultured with suboptimal mitogenic stimulation.
- The presence of CD40L enhanced IL-2 production and increased the expression of activation markers IL-2R alpha and CD69 on T cells.
- These results demonstrate CD40L's potent T cell activating capacity.
Conclusions:
- CD40L is a potent activator of murine T cells, independent of B cell co-stimulation.
- CD40L enhances T cell responses during suboptimal activation, suggesting a role in T:T cell interactions.
- The findings indicate CD40L is involved in the regulation of T cell function within the immune system.
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