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Updated: Aug 14, 2026

Isolation and Activation of Murine Lymphocytes
Published on: October 30, 2016
Interleukin-12-dependent activation of human lymphocyte subsets
O J Cordero1, F J Salgado, J E Viñuela
1Department of Biochemistry and Molecular Biology, University of Santiago de Compostela, Spain. bnojcord@usc.es
Insights
Interleukin-12 (IL-12) enhances CD8 T cell proliferation and CD26 expression in activated T cells. This finding suggests a novel pathway for T-helper 1 (Th1) immune responses with potential clinical applications.
Area of Science:
- Immunology
- Cell Biology
Background:
- Interleukin-12 (IL-12) is known to influence T-helper 1 (Th1) immune responses.
- Previous research indicated IL-12 increases CD26/dipeptidyl peptidase IV (DPPIV) expression and function, suggesting a new cellular pathway.
Purpose of the Study:
- To identify specific T cell subsets that respond to IL-12-induced CD26 upregulation.
- To investigate the effects of IL-12 on T cell proliferation and CD26 expression under specific culture conditions.
Main Methods:
- Utilized dual fluorescence analysis to examine CD26 expression on activated T cells.
- Cultured T cells with phytohemagglutinin (PHA) and IL-12 to assess proliferation and marker expression.
Main Results:
- IL-12 preferentially enhanced CD8 T cell proliferation, contrasting with some previous findings.
- IL-12-dependent CD26 expression was observed on both CD4 and CD8 activated T cells.
- While the percentage of CD45RO+ cells remained unaffected, the density of CD45RO antigen expression was reduced.
Conclusions:
- IL-12 modulates T cell subsets, notably enhancing CD8 T cell proliferation and influencing CD26 and CD45RO expression.
- These immunomodulatory effects of IL-12 may have implications for Th1-like immune responses.
- The findings suggest potential clinical applications for IL-12 in immune modulation.
Abstract:
Recently, we reported that IL-12 increased expression and function of CD26/DPPIV, this may be a new cellular pathway of the Th1-like immune responses. Here, we looked for a specific subset which would respond to CD26 upregulation by IL-12. Contrary to previously described results, under our culture conditions (1 microg/ml of PHA), IL-12 enhanced preferentially the CD8 cell proliferation. By using dual fluorescence analysis, IL-12-dependent CD26 expression was found in both CD4 and CD8 (previously CD26+ or CD26-) activated T cells and, moreover, the CD45RO percentage was unaffected. However, the density of CD45RO Ag (which was reported to coexpress with CD26) was impaired. These effects can be implicated in the biological functions of IL-12 and provide some clinical possibilities.
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