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Updated: Jul 13, 2026

Generation of Induced Regulatory T Cells from Primary Human Naïve and Memory T Cells
Published on: April 16, 2012
CD30-mediated signaling promotes the development of human T helper type 2-like T cells
G Del Prete1, M De Carli, M M D'Elios
1Division of Clinical Immunology and Allergy, University of Florence, Italy.
Insights
CD30 signaling promotes T helper type 2 (Th2) immune responses. Activating CD30 on T cells enhances their proliferation and cytokine production, favoring Th2 development and suppressing Th1-like responses.
Area of Science:
- Immunology
- Cellular Biology
Background:
- CD30 is a receptor on activated T cells, part of the tumor necrosis factor receptor superfamily.
- Previous work indicated CD30 expression on T helper type 2 (Th2) cytokine-producing T cell clones.
Purpose of the Study:
- To investigate the role of CD30 costimulation in T cell activation and differentiation.
- To determine if CD30 signaling influences the development of Th1 versus Th2 immune responses.
Main Methods:
- Using agonistic anti-CD30 monoclonal antibodies to costimulate established human Th2 and Th0 T cell clones.
- Analyzing antigen-induced proliferation and cytokine secretion.
- Costimulating peripheral blood mononuclear cells (PBMCs) and assessing the resulting T cell lines and clones.
- Blocking CD30 ligand-CD30 interactions in bulk cultures.
Main Results:
- Costimulation with anti-CD30 enhanced proliferation and cytokine secretion in established Th2 and Th0 clones.
- Anti-CD30 treatment of PBMCs led to preferential development of Th2-like T cell lines and clones.
- Blocking CD30-CD30L interaction shifted T cell development towards a Th1-like phenotype.
Conclusions:
- CD30 triggering acts as a costimulatory signal for activated T cells.
- CD30 signaling promotes the development of Th2-type immune responses.
- CD30-CD30L interactions on antigen-presenting cells are crucial for directing T cell polarization.
Abstract:
We have recently shown that CD30, a member of the tumor necrosis factor/nerve growth factor receptor superfamily, is preferentially expressed by human T cell clones producing T helper (Th) type 2 cytokines. We report here that costimulation with an agonistic anti-CD30 monoclonal antibody enhanced antigen (Ag)-induced proliferation and cytokine secretion by established human Th2 and Th0 clones. Moreover, costimulation of peripheral blood mononuclear cells with the same anti-CD30 monoclonal antibody resulted in the preferential development of Ag-specific T cell lines and clones showing a Th2-like profile of cytokine secretion. In contrast, early blockade in bulk culture of CD30 ligand-CD30 interaction shifted the development of Ag-specific T cells towards the opposite (Th1-like) phenotype. Taken together, these data suggest that CD30 triggering of activated Th cells by CD30 ligand-expressing Ag-presenting cells may represent an important costimulatory signaling for the development of Th2-type responses.
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