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Generation of Induced Regulatory T Cells from Primary Human Naïve and Memory T Cells
Published on: April 16, 2012
CD4+CD25+ regulatory cells in acquired MHC tolerance
E H Field1, D Matesic, S Rigby
1Department of Veterans Affairs Medical Center, Iowa City, Iowa 52246, USA. liz-field@icva.gov
Immunological Reviews
|November 28, 2001
Summary
Regulatory CD4+CD25+ cells induce tolerance to foreign MHC antigens. These cells prevent the development of CD8+ T-cell responses, crucial for acquired self-tolerance.
Area of Science:
- Immunology
- Transplantation Immunology
Background:
- Self-tolerance is maintained by central and peripheral mechanisms.
- Regulatory CD4+ T cells are key in controlling immune responses to self-antigens.
- Neonatal exposure to foreign MHC antigens induces tolerance, serving as a model for acquired self-tolerance.
Purpose of the Study:
- To investigate the role of regulatory CD4+ T cells in acquired tolerance to foreign MHC antigens.
- To determine if regulatory CD4+ T cells can prevent T-cell alloreactivity.
Main Methods:
- Adoptive transfer of spleen cells from neonatally tolerant mice into SCID recipients.
- Assessment of skin graft rejection.
- In vitro assays including cytotoxic T-lymphocyte assays, ELISPOT, and flow cytometry to analyze CD8+ T-cell effector function.
Main Results:
- Adoptive transfer of unfractionated spleen cells from tolerant mice inhibited skin graft rejection.
- CD4+CD25+ cells from tolerant mice suppressed the development of anti-donor CD8+ T-cell responses in vitro.
- Evidence of CD4+CD25+ regulatory cells mediating tolerance to foreign MHC.
Conclusions:
- Regulatory CD4+CD25+ cells play a critical role in initiating and maintaining tolerance to foreign MHC antigens.
- These regulatory cells prevent the development of CD8+ T-cell alloreactivity, contributing to acquired self-tolerance.
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