Abstract
The phenomenon of T-cell allorecognition of foreign major histocompatibility molecules has been one of the more enigmatic aspects of T-cell immunology. The molecular basis for allorecognition is unfolding as a result of the application of major histocompatibility complex structure/function analyses in the light of current insights into the three-dimensional structure of major histocompatibility complex products.
MeSH terms
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Animals
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Histocompatibility Antigens Class I / immunology
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Histocompatibility Antigens Class II / immunology
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Humans
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Immunity, Cellular*
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Isoantigens / immunology
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Major Histocompatibility Complex*
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Peptide Fragments / immunology
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Polymorphism, Genetic
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Protein Conformation
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Receptors, Antigen, T-Cell / immunology
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Structure-Activity Relationship
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T-Lymphocytes / immunology*
Substances
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Histocompatibility Antigens Class I
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Histocompatibility Antigens Class II
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Isoantigens
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Peptide Fragments
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Receptors, Antigen, T-Cell