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Successful treatment of autoimmunity in NZB/NZW F1 mice with monoclonal antibody to L3T4

Autoimmune NZB/NZW mice were treated with weekly injections of monoclonal antibody (mAb) to L3T4, an antigen expressed on a distinct subpopulation of T cells that respond to class II major histocompatibility antigens. Treatment with anti-L3T4 depleted circulating target cells, reduced autoantibody p...

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Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1985
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2187572/
https://www.ncbi.nlm.nih.gov/pubmed/3919141
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description Autoimmune NZB/NZW mice were treated with weekly injections of monoclonal antibody (mAb) to L3T4, an antigen expressed on a distinct subpopulation of T cells that respond to class II major histocompatibility antigens. Treatment with anti-L3T4 depleted circulating target cells, reduced autoantibody production, retarded renal disease, and prolonged life relative to control mice treated either with saline or with purified nonimmune rat IgG. These findings establish that autoimmune disease in NZB/NZW mice is regulated by T cells. In contrast to mice treated with nonimmune rat IgG, mice treated with rat anti-L3T4 mAb developed little or no antibody to rat Ig. Thus, the benefits of treatment with anti-L3T4 were achieved while minimizing the risks associated with a host immune response to therapy. This study raises the possibility that treatment with mAb against Leu-3/T4, the human homologue for L3T4 might be effective in the treatment of certain autoimmune diseases in people.
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spelling pubmed-21875722008-04-17 Successful treatment of autoimmunity in NZB/NZW F1 mice with monoclonal antibody to L3T4 J Exp Med Articles Autoimmune NZB/NZW mice were treated with weekly injections of monoclonal antibody (mAb) to L3T4, an antigen expressed on a distinct subpopulation of T cells that respond to class II major histocompatibility antigens. Treatment with anti-L3T4 depleted circulating target cells, reduced autoantibody production, retarded renal disease, and prolonged life relative to control mice treated either with saline or with purified nonimmune rat IgG. These findings establish that autoimmune disease in NZB/NZW mice is regulated by T cells. In contrast to mice treated with nonimmune rat IgG, mice treated with rat anti-L3T4 mAb developed little or no antibody to rat Ig. Thus, the benefits of treatment with anti-L3T4 were achieved while minimizing the risks associated with a host immune response to therapy. This study raises the possibility that treatment with mAb against Leu-3/T4, the human homologue for L3T4 might be effective in the treatment of certain autoimmune diseases in people. The Rockefeller University Press 1985-02-01 /pmc/articles/PMC2187572/ /pubmed/3919141 Text en This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/).
spellingShingle Articles
Successful treatment of autoimmunity in NZB/NZW F1 mice with monoclonal antibody to L3T4
title Successful treatment of autoimmunity in NZB/NZW F1 mice with monoclonal antibody to L3T4
title_full Successful treatment of autoimmunity in NZB/NZW F1 mice with monoclonal antibody to L3T4
title_fullStr Successful treatment of autoimmunity in NZB/NZW F1 mice with monoclonal antibody to L3T4
title_full_unstemmed Successful treatment of autoimmunity in NZB/NZW F1 mice with monoclonal antibody to L3T4
title_short Successful treatment of autoimmunity in NZB/NZW F1 mice with monoclonal antibody to L3T4
title_sort successful treatment of autoimmunity in nzb/nzw f1 mice with monoclonal antibody to l3t4
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2187572/
https://www.ncbi.nlm.nih.gov/pubmed/3919141