Major histocompatibility complex binding affinity of an antigenic determinant is crucial for the differential secretion of interleukin 4/5 or interferon gamma by T cells
Autor: | Eli E. Sercarz, Luis R. B. Soares, J. I. Alexander, Alessandro Sette, Vatsala Bhardwaj, Vipin Kumar |
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Rok vydání: | 1995 |
Předmět: |
T-Lymphocytes
Molecular Sequence Data Biology Major Histocompatibility Complex Epitopes Interferon-gamma Mice Antigen Interferon medicine Animals Interferon gamma Secretion Amino Acid Sequence Interleukin 4 Multidisciplinary Dose-Response Relationship Drug Interferon-gamma production Histocompatibility Antigens Class II Lymphokine Interleukin Myelin Basic Protein Molecular biology Peptide Fragments Cytokines Female Interleukin-4 Interleukin-5 Protein Binding Research Article medicine.drug |
Zdroj: | Proceedings of the National Academy of Sciences. 92:9510-9514 |
ISSN: | 1091-6490 0027-8424 |
DOI: | 10.1073/pnas.92.21.9510 |
Popis: | Differential activation of CD4+ T-cell precursors in vivo leads to the development of effectors with unique patterns of lymphokine secretion. To investigate whether the differential pattern of lymphokine secretion is influenced by factors associated with either the display and/or recognition of the ligand, we have used a set of ligands with various class II binding affinities but unchanged T-cell specificity. The ligand that exhibited approximately 10,000-fold higher binding to I-Au considerably increased the frequency of interferon gamma-producing but not interleukin (IL) 4- or IL-5-secreting cells in vivo. Using an established ligand-specific, CD4+ T-cell clone secreting only IL-4, we also demonstrated that stimulation with the highest affinity ligand resulted in interferon gamma production in vitro. In contrast, ligands that demonstrated relatively lower class II binding induced only IL-4 secretion. These data suggest that the major histocompatibility complex binding affinity of antigenic determinants, leading to differential interactions at the T cell-antigen-presenting cell interface, can be crucial for the differential development of cytokine patterns in T cells. |
Databáze: | OpenAIRE |
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