Selection of a Broad Repertoire of CD4+ T Cells in H-2Ma0/0 Mice
pmid: 9285404
Selection of a Broad Repertoire of CD4+ T Cells in H-2Ma0/0 Mice
According to past reports, H-2Ma0/0 mice express a single major histocompatiblity complex class II molecule, A(b), heavily loaded with a single peptide derived from the invariant chain, CLIP. Despite the highly restricted diversity of the class II:peptide complexes expressed on thymic stromal cells in the mutant animals, a large and diverse population of CD4+ T cells is positively selected. However, two important issues remained unresolved and are addressed here: Just how preponderant is CLIP occupancy of the class II molecules from H-2M0/0 mice? How extensive and functionally competent is the CD4+ population selected in the mutant animals? Our results argue that a single class II:peptide complex can select a very broad, though not complete, repertoire of CD4+ T cells.
- Inserm France
- French Institute of Health and Medical Research France
- French National Centre for Scientific Research France
- University of Zurich Switzerland
- Institute of Genetics and Molecular and Cellular Biology France
CD4-Positive T-Lymphocytes, Mice, Knockout, Antigen Presentation, Superantigens, Receptors, Antigen, T-Cell, alpha-beta, Immunology, H-2 Antigens, Histocompatibility Antigens Class II, Epitopes, T-Lymphocyte, Cell Differentiation, Mice, Transgenic, Antigens, Differentiation, B-Lymphocyte, Mice, Inbred C57BL, Mice, Infectious Diseases, Antigens, CD, Bone Marrow, Radiation Chimera, Immunology and Allergy, Animals, Peptides
CD4-Positive T-Lymphocytes, Mice, Knockout, Antigen Presentation, Superantigens, Receptors, Antigen, T-Cell, alpha-beta, Immunology, H-2 Antigens, Histocompatibility Antigens Class II, Epitopes, T-Lymphocyte, Cell Differentiation, Mice, Transgenic, Antigens, Differentiation, B-Lymphocyte, Mice, Inbred C57BL, Mice, Infectious Diseases, Antigens, CD, Bone Marrow, Radiation Chimera, Immunology and Allergy, Animals, Peptides
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