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Anti-ergotypic T cells in naïve rats
Avishai Mimran1, Felix Mor, Francisco J Quintana
1Department of Immunology, The Weizmann Institute of Science, Herzel street, Rehovot 76100, Israel.
Journal of Autoimmunity
|April 26, 2005
Summary
Anti-ergotypic T cells, a regulatory T cell subset, are present in naive rats and respond to activated T cells. These CD8+ T cells, including TCRgamma/delta+ and TCRalpha/beta+ types, suggest a role in immune regulation.
Area of Science:
- Immunology
- Cellular Immunology
- T cell biology
Background:
- T regulatory cells are crucial for immune homeostasis.
- Anti-ergotypic T cells are a subset of regulatory T cells that recognize T cell activation markers (ergotopes).
Purpose of the Study:
- To investigate the presence and characteristics of anti-ergotypic T cells in naive animals.
- To elucidate the phenotype and functional properties of these regulatory T cells.
Main Methods:
- Analysis of T cell populations in lymph nodes, spleens, and thymuses of naive rats.
- Phenotypic characterization using flow cytometry (CD8, TCRalpha/beta, TCRgamma/delta).
- Assessment of proliferative responses and cytokine secretion (IFNgamma, TNFalpha) upon co-culture with activated T cells.
Main Results:
- Anti-ergotypic T cells were found in naive rat lymphoid organs, with development independent of antigen priming.
- These cells were CD8+, encompassing both TCRalpha/beta+ and TCRgamma/delta+ subsets.
- TCRgamma/delta+ cells secreted IFNgamma and TNFalpha, while TCRalpha/beta+ cells proliferated without significant cytokine secretion.
- Cell-cell contact was required, independent of professional APCs.
- TCRalpha/beta+CD8+ responses were MHC-I restricted and B7-CD28 dependent; TCRgamma/delta+ responses were B7-CD28 dependent but MHC-independent.
Conclusions:
- The presence of anti-ergotypic T cells in naive animals indicates a potential intrinsic role in immune regulation and maintenance.
- These distinct T cell subsets may contribute to self-tolerance and control of immune responses from birth.