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dc.contributor.authorRashighi, Medhi
dc.contributor.authorHarris, John E.
dc.date2022-08-11T08:09:20.000
dc.date.accessioned2022-08-23T16:27:06Z
dc.date.available2022-08-23T16:27:06Z
dc.date.issued2017-04-01
dc.date.submitted2017-05-25
dc.identifier.citationDermatol Clin. 2017 Apr;35(2):257-265. doi: 10.1016/j.det.2016.11.014. <a href="https://doi.org/10.1016/j.det.2016.11.014">Link to article on publisher's site</a>
dc.identifier.issn0733-8635 (Linking)
dc.identifier.doi10.1016/j.det.2016.11.014
dc.identifier.pmid28317534
dc.identifier.urihttp://hdl.handle.net/20.500.14038/36708
dc.description.abstractThe pathogenesis of vitiligo involves interplay between intrinsic and extrinsic melanocyte defects, innate immune inflammation, and T-cell-mediated melanocyte destruction. The goal of treatment is to not only halt disease progression but also promote repigmentation through melanocyte regeneration, proliferation, and migration. Treatment strategies that address all aspects of disease pathogenesis and repigmentation are likely to have greatest efficacy, a strategy that may require combination therapies. Current treatments generally involve nontargeted suppression of autoimmunity, whereas emerging treatments are likely to use a more targeted approach based on in-depth understanding of disease pathogenesis, which may provide higher efficacy with a good safety profile.
dc.language.isoen_US
dc.relation<a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=28317534&dopt=Abstract">Link to Article in PubMed</a>
dc.relation.urlhttps://doi.org/10.1016/j.det.2016.11.014
dc.subjectAutoimmunity
dc.subjectCellular stress
dc.subjectChemokines
dc.subjectMelanogenesis
dc.subjectTargeted therapy
dc.subjectVitiligo
dc.subjectCellular and Molecular Physiology
dc.subjectDermatology
dc.subjectSkin and Connective Tissue Diseases
dc.titleVitiligo Pathogenesis and Emerging Treatments
dc.typeJournal Article
dc.source.journaltitleDermatologic clinics
dc.source.volume35
dc.source.issue2
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/metnet_pubs/76
dc.identifier.contextkey10212139
html.description.abstract<p>The pathogenesis of vitiligo involves interplay between intrinsic and extrinsic melanocyte defects, innate immune inflammation, and T-cell-mediated melanocyte destruction. The goal of treatment is to not only halt disease progression but also promote repigmentation through melanocyte regeneration, proliferation, and migration. Treatment strategies that address all aspects of disease pathogenesis and repigmentation are likely to have greatest efficacy, a strategy that may require combination therapies. Current treatments generally involve nontargeted suppression of autoimmunity, whereas emerging treatments are likely to use a more targeted approach based on in-depth understanding of disease pathogenesis, which may provide higher efficacy with a good safety profile.</p>
dc.identifier.submissionpathmetnet_pubs/76
dc.contributor.departmentUMass Metabolic Network
dc.contributor.departmentDepartment of Medicine, Division of Dermatology
dc.source.pages257-265


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