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dc.contributor.authorHarris, John E.
dc.date2022-08-11T08:09:20.000
dc.date.accessioned2022-08-23T16:27:03Z
dc.date.available2022-08-23T16:27:03Z
dc.date.issued2016-01-01
dc.date.submitted2017-04-20
dc.identifier.citationImmunol Rev. 2016 Jan;269(1):11-25. doi: 10.1111/imr.12369. <a href="https://doi.org/10.1111/imr.12369">Link to article on publisher's site</a>
dc.identifier.issn0105-2896 (Linking)
dc.identifier.doi10.1111/imr.12369
dc.identifier.pmid26683142
dc.identifier.urihttp://hdl.handle.net/20.500.14038/36693
dc.description.abstractFor decades, research in autoimmunity has focused primarily on immune contributions to disease. Yet recent studies report elevated levels of reactive oxygen species and abnormal activation of the unfolded protein response in cells targeted by autoimmunity, implicating cellular stress originating from the target tissue as a contributing factor. A better understanding of this contribution may help to answer important lingering questions in organ-specific autoimmunity, as to what factors initiate disease and what directs its tissue specificity. Vitiligo, an autoimmune disease of the skin, has been the focus of translational research for over 30 years, and both melanocyte stress and immune mechanisms have been thought to be mutually exclusive explanations for pathogenesis. Chemical-induced vitiligo is a unique clinical presentation that reflects the importance of environmental influences on autoimmunity, provides insight into a new paradigm linking cell stress to the immune response, and serves as a template for other autoimmune diseases. In this review, I will discuss the evidence for cell stress contributions to a number of autoimmune diseases, the questions that remain, and how vitiligo, an underappreciated example of organ-specific autoimmunity, helps to answer them.
dc.language.isoen_US
dc.relation<a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=26683142&dopt=Abstract">Link to Article in PubMed</a>
dc.relation.urlhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4685729/
dc.subjectCell Biology
dc.subjectCellular and Molecular Physiology
dc.subjectImmune System Diseases
dc.subjectImmunity
dc.titleCellular stress and innate inflammation in organ-specific autoimmunity: lessons learned from vitiligo
dc.typeJournal Article
dc.source.journaltitleImmunological reviews
dc.source.volume269
dc.source.issue1
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/metnet_pubs/60
dc.identifier.contextkey10048082
html.description.abstract<p>For decades, research in autoimmunity has focused primarily on immune contributions to disease. Yet recent studies report elevated levels of reactive oxygen species and abnormal activation of the unfolded protein response in cells targeted by autoimmunity, implicating cellular stress originating from the target tissue as a contributing factor. A better understanding of this contribution may help to answer important lingering questions in organ-specific autoimmunity, as to what factors initiate disease and what directs its tissue specificity. Vitiligo, an autoimmune disease of the skin, has been the focus of translational research for over 30 years, and both melanocyte stress and immune mechanisms have been thought to be mutually exclusive explanations for pathogenesis. Chemical-induced vitiligo is a unique clinical presentation that reflects the importance of environmental influences on autoimmunity, provides insight into a new paradigm linking cell stress to the immune response, and serves as a template for other autoimmune diseases. In this review, I will discuss the evidence for cell stress contributions to a number of autoimmune diseases, the questions that remain, and how vitiligo, an underappreciated example of organ-specific autoimmunity, helps to answer them.</p>
dc.identifier.submissionpathmetnet_pubs/60
dc.contributor.departmentUMass Metabolic Network
dc.contributor.departmentDepartment of Medicine, Division of Dermatology
dc.source.pages11-25


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