Iat epitopes on T cell receptor for self MHC class II determinants
Language English Country Czech Republic Media print
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
2470623
Knihovny.cz E-resources
- MeSH
- Lymphocyte Activation MeSH
- Epitopes immunology MeSH
- H-2 Antigens immunology MeSH
- Immune Tolerance * MeSH
- Mice, Inbred Strains genetics immunology MeSH
- Crosses, Genetic MeSH
- Histocompatibility Antigens Class II immunology MeSH
- Antibodies, Monoclonal immunology MeSH
- Mice MeSH
- Receptors, Antigen, T-Cell * MeSH
- T-Lymphocytes immunology MeSH
- Lymphocyte Culture Test, Mixed MeSH
- Animals MeSH
- Check Tag
- Mice MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Epitopes MeSH
- H-2 Antigens MeSH
- Histocompatibility Antigens Class II MeSH
- Antibodies, Monoclonal MeSH
- Receptors, Antigen, T-Cell * MeSH
Anti-Iatk monoclonal antibodies (mAbs) were found to inhibit syngeneic mixed lymphocyte reaction (SMLR) of mice with k and a haplotypes (H-2k and H-2a) of the major histocompatibility complex (MHC) by acting on responder T cells but not stimulator cells. Only the early phase of SMLR was inhibited by anti-Iat mAbs. The inhibitory effect was due to the blocking of autoreactive T cells but not induction of suppressor lymphocytes. Cross-linking of Iat epitopes induced T cell proliferation of k haplotype strain. The inhibitory pattern of SMLR by four anti-Iat mAbs varied among different strains of mice. The inhibitory pattern seemed to depend on MHC and unidentified non-MHC background genes possessed by stimulator cells, suggesting that the shape of the MHC recognition site must have different conformation depending on both MHC and non-MHC gene products recognized. However, the inhibitory pattern of SMLR by anti-Iat mAbs of strains which differ at the I-J locus: B10.A(5R) and B10.A(3R) was dependent on the genotype of stimulator cells. The same was observed in B10.S(9R) and B10.HTT strains. The inhibitory activity of anti-Iat mAbs was entirely directed against responder T cells and was not passively carried out by the stimulators. It was concluded that Iat epitopes are I region controlled determinants that are utilized by T cells as receptors for self Ia antigens. It is suggested that anti-Iat mAbs react with an idiotype on the receptor(s) for Ia or I-J, or possibly a "receptor" for these receptors.