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TNF Receptor 2 and Disease: Autoimmunity and Regenerative Medicine

The regulatory cytokine tumor necrosis factor (TNF) exerts its effects through two receptors: TNFR1 and TNFR2. Defects in TNFR2 signaling are evident in a variety of autoimmune diseases. One new treatment strategy for autoimmune disease is selective destruction of autoreactive T cells by administrat...

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Autores principales: Faustman, Denise L., Davis, Miriam
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3870411/
https://www.ncbi.nlm.nih.gov/pubmed/24391650
http://dx.doi.org/10.3389/fimmu.2013.00478
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author Faustman, Denise L.
Davis, Miriam
author_facet Faustman, Denise L.
Davis, Miriam
author_sort Faustman, Denise L.
collection PubMed
description The regulatory cytokine tumor necrosis factor (TNF) exerts its effects through two receptors: TNFR1 and TNFR2. Defects in TNFR2 signaling are evident in a variety of autoimmune diseases. One new treatment strategy for autoimmune disease is selective destruction of autoreactive T cells by administration of TNF, TNF inducers, or TNFR2 agonism. A related strategy is to rely on TNFR2 agonism to induce T-regulatory cells (T(regs)) that suppress cytotoxic T cells. Targeting TNFR2 as a treatment strategy is likely superior to TNFR1 because of its more limited cellular distribution on T cells, subsets of neurons, and a few other cell types, whereas TNFR1 is expressed throughout the body. This review focuses on TNFR2 expression, structure, and signaling; TNFR2 signaling in autoimmune disease; treatment strategies targeting TNFR2 in autoimmunity; and the potential for TNFR2 to facilitate end organ regeneration.
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spelling pubmed-38704112014-01-03 TNF Receptor 2 and Disease: Autoimmunity and Regenerative Medicine Faustman, Denise L. Davis, Miriam Front Immunol Immunology The regulatory cytokine tumor necrosis factor (TNF) exerts its effects through two receptors: TNFR1 and TNFR2. Defects in TNFR2 signaling are evident in a variety of autoimmune diseases. One new treatment strategy for autoimmune disease is selective destruction of autoreactive T cells by administration of TNF, TNF inducers, or TNFR2 agonism. A related strategy is to rely on TNFR2 agonism to induce T-regulatory cells (T(regs)) that suppress cytotoxic T cells. Targeting TNFR2 as a treatment strategy is likely superior to TNFR1 because of its more limited cellular distribution on T cells, subsets of neurons, and a few other cell types, whereas TNFR1 is expressed throughout the body. This review focuses on TNFR2 expression, structure, and signaling; TNFR2 signaling in autoimmune disease; treatment strategies targeting TNFR2 in autoimmunity; and the potential for TNFR2 to facilitate end organ regeneration. Frontiers Media S.A. 2013-12-23 /pmc/articles/PMC3870411/ /pubmed/24391650 http://dx.doi.org/10.3389/fimmu.2013.00478 Text en Copyright © 2013 Faustman and Davis. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
Faustman, Denise L.
Davis, Miriam
TNF Receptor 2 and Disease: Autoimmunity and Regenerative Medicine
title TNF Receptor 2 and Disease: Autoimmunity and Regenerative Medicine
title_full TNF Receptor 2 and Disease: Autoimmunity and Regenerative Medicine
title_fullStr TNF Receptor 2 and Disease: Autoimmunity and Regenerative Medicine
title_full_unstemmed TNF Receptor 2 and Disease: Autoimmunity and Regenerative Medicine
title_short TNF Receptor 2 and Disease: Autoimmunity and Regenerative Medicine
title_sort tnf receptor 2 and disease: autoimmunity and regenerative medicine
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3870411/
https://www.ncbi.nlm.nih.gov/pubmed/24391650
http://dx.doi.org/10.3389/fimmu.2013.00478
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