Interleukin-2 can prevent and reverse antigen-induced unresponsiveness in cloned human T lymphocytes.

The exposure of human T-cell clones to supra-immunogenic concentrations of peptide antigen in the absence of accessory cells induces antigen-specific unresponsiveness. Using this model we have investigated the ability of cytokines to modulate the induction of, or reversal of, T-cell tolerance. Our f...

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Manylion Llyfryddiaeth
Prif Awduron: Essery, G, Feldmann, M, Lamb, JR
Fformat: Journal article
Iaith:English
Cyhoeddwyd: 1988
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author Essery, G
Feldmann, M
Lamb, JR
author_facet Essery, G
Feldmann, M
Lamb, JR
author_sort Essery, G
collection OXFORD
description The exposure of human T-cell clones to supra-immunogenic concentrations of peptide antigen in the absence of accessory cells induces antigen-specific unresponsiveness. Using this model we have investigated the ability of cytokines to modulate the induction of, or reversal of, T-cell tolerance. Our findings demonstrate that interleukin-2 (IL-2), but not interferon-gamma (IFN-gamma) or interleukin-1 (IL-1), is able to inhibit the induction of T-cell unresponsiveness in a dose-dependent fashion. Moreover, IL-2 was able to reverse established antigen-dependent T-cell unresponsiveness. In order to determine if modulation of IL-2 receptors is able to induce or abrogate unresponsiveness, the T cells were treated with anti-Tac antibody alone or together with tolerizing concentrations of antigen. Anti-Tac antibody was neither able to induce nor inhibit the induction of tolerance. The application of this model in the manipulation of immune responses is discussed here.
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spelling oxford-uuid:d463e45d-10b4-4a10-b947-cc4e6493f60a2022-03-27T08:18:12ZInterleukin-2 can prevent and reverse antigen-induced unresponsiveness in cloned human T lymphocytes.Journal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:d463e45d-10b4-4a10-b947-cc4e6493f60aEnglishSymplectic Elements at Oxford1988Essery, GFeldmann, MLamb, JRThe exposure of human T-cell clones to supra-immunogenic concentrations of peptide antigen in the absence of accessory cells induces antigen-specific unresponsiveness. Using this model we have investigated the ability of cytokines to modulate the induction of, or reversal of, T-cell tolerance. Our findings demonstrate that interleukin-2 (IL-2), but not interferon-gamma (IFN-gamma) or interleukin-1 (IL-1), is able to inhibit the induction of T-cell unresponsiveness in a dose-dependent fashion. Moreover, IL-2 was able to reverse established antigen-dependent T-cell unresponsiveness. In order to determine if modulation of IL-2 receptors is able to induce or abrogate unresponsiveness, the T cells were treated with anti-Tac antibody alone or together with tolerizing concentrations of antigen. Anti-Tac antibody was neither able to induce nor inhibit the induction of tolerance. The application of this model in the manipulation of immune responses is discussed here.
spellingShingle Essery, G
Feldmann, M
Lamb, JR
Interleukin-2 can prevent and reverse antigen-induced unresponsiveness in cloned human T lymphocytes.
title Interleukin-2 can prevent and reverse antigen-induced unresponsiveness in cloned human T lymphocytes.
title_full Interleukin-2 can prevent and reverse antigen-induced unresponsiveness in cloned human T lymphocytes.
title_fullStr Interleukin-2 can prevent and reverse antigen-induced unresponsiveness in cloned human T lymphocytes.
title_full_unstemmed Interleukin-2 can prevent and reverse antigen-induced unresponsiveness in cloned human T lymphocytes.
title_short Interleukin-2 can prevent and reverse antigen-induced unresponsiveness in cloned human T lymphocytes.
title_sort interleukin 2 can prevent and reverse antigen induced unresponsiveness in cloned human t lymphocytes
work_keys_str_mv AT esseryg interleukin2canpreventandreverseantigeninducedunresponsivenessinclonedhumantlymphocytes
AT feldmannm interleukin2canpreventandreverseantigeninducedunresponsivenessinclonedhumantlymphocytes
AT lambjr interleukin2canpreventandreverseantigeninducedunresponsivenessinclonedhumantlymphocytes