International Immunology, Vol. 2, No. 11, pp. 1063-1071,November 1990
© 1990 Japanese Society for Immunology
Murine suppressor T cell clones specific for minor histocompatibility antigens express CD4, CD8, and
ß T cell receptor molecules
ICRF Tumour Immunology Unit, Department of Biology, Medawar Building, University College London Gower Street, London WC1E 6BT, UK
1 Neuroimmunology Programme, Department of Biology, Medawar Building, University College London Gower Street, London WC1E 6BT, UK
Correspondence to: Correspondence to (present address): N. K. Nanda, Department of Microbiology and Molecular Genetics, 5304 Life Sciences, University of California, Los Angeles, CA 90024, USA
We have been able to establish stable, minor histocompatibility antigen-specific, non-cytolytic, MHC-class ll-restricted suppressor T cell clones and lines. These suppressor T cells rearrange, transcribe, and express
ß T cell receptor. An unusual feature of all our clones and lines is the co-expression of CD4 and CD8 molecules on their cell surface, a characteristic which may distinguish them from conventional helper and cytolytic T cells in this system. The fact that multiple, phenotyplcally and functionally Identical cell lines were reproducibly obtained from this system indicates that antigen-specific down-regulation of Immune functions In certain circumstances Is mediated by T cells that are neither conventional cytolytic nor helper T cells.
Received 13 July 1990, accepted 13 August 1990.
![]()
CiteULike
Connotea
Del.icio.us What's this?
This article has been cited by other articles:
![]() |
Y. Peng, H. Shao, Y. Ke, P. Zhang, G. Han, H. J. Kaplan, and D. Sun Minimally Activated CD8 Autoreactive T Cells Specific for IRBP Express a High Level of Foxp3 and Are Functionally Suppressive Invest. Ophthalmol. Vis. Sci., May 1, 2007; 48(5): 2178 - 2184. [Abstract] [Full Text] [PDF] |
||||
