Antigen Presentation and T Cell Development in H2-M-Deficient Mice
- 1 March 1996
- journal article
- other
- Published by American Association for the Advancement of Science (AAAS) in Science
- Vol. 271 (5253), 1278-1281
- https://doi.org/10.1126/science.271.5253.1278
Abstract
HLA-DM (DM) facilitates peptide loading of major histocompatibility complex class II molecules in human cell lines. Mice lacking functional H2-M, the mouse equivalent of DM, have normal amounts of class II molecules at the cell surface, but most of these are associated with invariant chain-derived CLIP peptides. These mice contain large numbers of CD4+ T cells, which is indicative of positive selection in the thymus. Their CD4+ cells were unresponsive to self H2-M-deficient antigen-presenting cells (APCs) but were hyperreactive to wild-type APCs. H2-M-deficient APCs failed to elicit proliferative responses from wild-type T cells.Keywords
This publication has 23 references indexed in Scilit:
- T cell recognition of major histocompatibility complex class II complexes with invariant chain processing intermediates.The Journal of Experimental Medicine, 1995
- The structure of an intermediate in class II MHC maturation: CLIP bound to HLA-DR3Nature, 1995
- HLA-DM induces clip dissociation from MHC class II αβ dimers and facilitates peptide loadingCell, 1995
- Reduced thymic maturation but normal effector function of CD8+ T cells in CD8 beta gene-targeted mice.The Journal of Experimental Medicine, 1994
- Peptides determine the lifespan of MHC class II molecules in the antigen-presenting cellNature, 1994
- Mice lacking the MHC class II-associated invariant chainCell, 1993
- Exclusion of circulating T cells from the thymus does not apply in the neonatal period.The Journal of Experimental Medicine, 1993
- The human class II MHC protein HLA-DR1 assembles as empty αβ heterodimers in the absence of antigenic peptideCell, 1992
- A role for peptide in determining MHC class II structureNature, 1991
- Induction of Neonatal Tolerance to Mls a Antigens by CD8 + T CellsScience, 1990