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IDO2: A Pathogenic Mediator of Inflammatory Autoimmunity
Indoleamine 2,3-dioxygenase 2 (IDO2), a homolog of the better-studied tryptophan-catabolizing enzyme IDO1, is an immunomodulatory molecule with potential effects on various diseases including cancer and autoimmunity. Here, we review what is known about the direct connections between IDO2 and immune...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Libertas Academica
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5119657/ https://www.ncbi.nlm.nih.gov/pubmed/27891058 http://dx.doi.org/10.4137/CPath.S39930 |
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author | Merlo, Lauren M.F. Mandik-Nayak, Laura |
author_facet | Merlo, Lauren M.F. Mandik-Nayak, Laura |
author_sort | Merlo, Lauren M.F. |
collection | PubMed |
description | Indoleamine 2,3-dioxygenase 2 (IDO2), a homolog of the better-studied tryptophan-catabolizing enzyme IDO1, is an immunomodulatory molecule with potential effects on various diseases including cancer and autoimmunity. Here, we review what is known about the direct connections between IDO2 and immune function, particularly in relationship to autoimmune inflammatory disorders such as rheumatoid arthritis and lupus. Accumulating evidence indicates that IDO2 acts as a pro-inflammatory mediator of autoimmunity, with a functional phenotype distinct from IDO1. IDO2 is expressed in antigen-presenting cells, including B cells and dendritic cells, but affects inflammatory responses in the autoimmune context specifically by acting in B cells to modulate T cell help in multiple model systems. Given that expression of IDO2 can lead to exacerbation of inflammatory responses, IDO2 should be considered a potential therapeutic target for autoimmune disorders. |
format | Online Article Text |
id | pubmed-5119657 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Libertas Academica |
record_format | MEDLINE/PubMed |
spelling | pubmed-51196572016-11-26 IDO2: A Pathogenic Mediator of Inflammatory Autoimmunity Merlo, Lauren M.F. Mandik-Nayak, Laura Clin Med Insights Pathol Review Indoleamine 2,3-dioxygenase 2 (IDO2), a homolog of the better-studied tryptophan-catabolizing enzyme IDO1, is an immunomodulatory molecule with potential effects on various diseases including cancer and autoimmunity. Here, we review what is known about the direct connections between IDO2 and immune function, particularly in relationship to autoimmune inflammatory disorders such as rheumatoid arthritis and lupus. Accumulating evidence indicates that IDO2 acts as a pro-inflammatory mediator of autoimmunity, with a functional phenotype distinct from IDO1. IDO2 is expressed in antigen-presenting cells, including B cells and dendritic cells, but affects inflammatory responses in the autoimmune context specifically by acting in B cells to modulate T cell help in multiple model systems. Given that expression of IDO2 can lead to exacerbation of inflammatory responses, IDO2 should be considered a potential therapeutic target for autoimmune disorders. Libertas Academica 2016-11-21 /pmc/articles/PMC5119657/ /pubmed/27891058 http://dx.doi.org/10.4137/CPath.S39930 Text en © 2016 the author(s), publisher and licensee Libertas Academica Ltd. This is an open-access article distributed under the terms of the Creative Commons CC-BY-NC 3.0 License. |
spellingShingle | Review Merlo, Lauren M.F. Mandik-Nayak, Laura IDO2: A Pathogenic Mediator of Inflammatory Autoimmunity |
title | IDO2: A Pathogenic Mediator of Inflammatory Autoimmunity |
title_full | IDO2: A Pathogenic Mediator of Inflammatory Autoimmunity |
title_fullStr | IDO2: A Pathogenic Mediator of Inflammatory Autoimmunity |
title_full_unstemmed | IDO2: A Pathogenic Mediator of Inflammatory Autoimmunity |
title_short | IDO2: A Pathogenic Mediator of Inflammatory Autoimmunity |
title_sort | ido2: a pathogenic mediator of inflammatory autoimmunity |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5119657/ https://www.ncbi.nlm.nih.gov/pubmed/27891058 http://dx.doi.org/10.4137/CPath.S39930 |
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