Diversity of a human CD4+ T cell repertoire recognizing one TCR ligand
- 31 July 1996
- journal article
- research article
- Published by Elsevier in Immunology Letters
- Vol. 51 (3) , 191-194
- https://doi.org/10.1016/0165-2478(96)02545-x
Abstract
No abstract availableFunding Information
- Ministry of Education, Culture, Sports, Science and Technology
This publication has 14 references indexed in Scilit:
- Single amino acid substitutions on a Japanese cedar pollen allergen (Cry j 1)-derived peptide induced alterations in human T cell responses and T cell receptor antagonismJournal of Allergy and Clinical Immunology, 1996
- Specific T cell recognition of minimally homologous peptides: Evidence for multiple endogenous LigandsImmunity, 1995
- Modulation of cytokine patterns of human autoreactive T cell clones by a single amino acid substitution of their peptide ligandImmunity, 1995
- Molecular mimicry in T cell-mediated autoimmunity: Viral peptides activate human T cell clones specific for myelin basic proteinCell, 1995
- Nomenclature for factors of the HLA system, 1994Human Immunology, 1994
- The expressed T cell receptor V gene repertoire of rheumatoid arthritis monozygotic twins: Rapid analysis by anchored polymerase chain reaction and enzyme‐linked immunosorbent assayEuropean Journal of Immunology, 1993
- Induction of T-cell anergy by altered T-cell-receptor ligand on live antigen-presenting cellsNature, 1993
- Peptide-major histocompatibility complex class II complexes with mixed agonist/antagonist properties provide evidence for ligand-related differences in T cell receptor-dependent intracellular signaling.The Journal of Experimental Medicine, 1993
- Preferential V beta gene usage and lack of junctional sequence conservation among human T cell receptors specific for a tetanus toxin-derived peptide: evidence for a dominant role of a germline-encoded V region in antigen/major histocompatibility complex recognition.The Journal of Experimental Medicine, 1992
- Separation of IL-4 Production from Th Cell Proliferation by an Altered T Cell Receptor LigandScience, 1991