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Updated: Jul 30, 2026

Generation of Human CD40-activated B cells
Published on: October 16, 2009
Anti-immunoglobulin and anti-CD40 stimulation induces CD25 expression by resting human tonsillar B lymphocytes
E L Burlinson1, H M Pringle, B W Ozanne
1Division of Biochemistry and Molecular Biology, University of Glasgow, Scotland, UK.
Insights
Interleukin-4 (IL-4) is the sole cytokine that induces CD25 expression on quiescent human B cells. Cross-linking B-cell receptors or CD40 also promotes CD25 expression, with anti-Ig being more potent than anti-CD40.
Area of Science:
- Immunology
- Cell Biology
Background:
- CD25 is the 55-kDa inducible component of the IL-2 receptor complex.
- CD25 is expressed on T and B lymphocytes.
Purpose of the Study:
- To investigate the effect of B-cell surface molecule ligation on CD25 expression.
- To identify cytokines and surface molecule stimulation that induce CD25 expression in human B cells.
Main Methods:
- Culturing high-density quiescent tonsillar B cells.
- Stimulating B cells with cytokines (IL-4, IL-10, IL-13) and antibodies against B-cell surface molecules (antigen receptors, CD40).
- Assessing CD25 expression using flow cytometry.
Main Results:
- Interleukin-4 (IL-4) was the only tested cytokine to induce CD25 expression in quiescent human B cells.
- Antibody-mediated cross-linking of antigen receptors (anti-Ig) or CD40 induced CD25 expression in a dose-dependent manner.
- Anti-Ig stimulation resulted in higher CD25 expression (≥80% of cells) compared to anti-CD40 (approx. 25% of cells).
- Combinations of stimuli showed additive but not synergistic effects on CD25 expression.
Conclusions:
- IL-4 is a key cytokine for inducing CD25 expression in quiescent human B cells.
- B-cell activation via antigen receptors or CD40 can also upregulate CD25 expression.
- Distinct signaling pathways may be involved in CD25 induction by different stimuli.
Abstract:
In this report, the effect of ligation of a number of B-cell surface molecules upon expression of CD25, the 55-kDa inducible component of the IL-2 receptor complex found on T and B lymphocytes, is reported. IL-4 is the only cytokine apparently capable of promoting CD25 expression in human high-density quiescent tonsillar B cells; neither IL-10 nor IL-13 could induce CD25 expression. Cross-linking of the antigen receptors or CD40 with antibody elicited CD25 expression in a dose-dependent manner. Stimulation with anti-CD40 promoted CD25 expression in approximately 25% of B cells, while anti-Ig caused 80% or more of cells to become CD25+. In experiments where the stimuli were used in combination, some additive effects upon CD25 expression were noted, but no obvious synergistic effects could be detected.
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