Variant of TYR and Autoimmunity Susceptibility Loci in Generalized Vitiligo
The results of a genomewide association study of generalized vitiligo implicate genes involved in the immune response and also a variant of TYR, which encodes tyrosinase. This variant of TYR encodes a protein that seems particularly likely to be detected by immune surveillance. The results of a geno...
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Published in: | The New England journal of medicine Vol. 362; no. 18; pp. 1686 - 1697 |
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Main Authors: | , , , , , , , , , , , , , , , , , , , , , , , , |
Format: | Journal Article |
Language: | English |
Published: |
Waltham, MA
Massachusetts Medical Society
06-05-2010
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Subjects: | |
Online Access: | Get full text |
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Summary: | The results of a genomewide association study of generalized vitiligo implicate genes involved in the immune response and also a variant of
TYR,
which encodes tyrosinase. This variant of
TYR
encodes a protein that seems particularly likely to be detected by immune surveillance.
The results of a genomewide association study of generalized vitiligo implicate genes involved in the immune response and also a variant of TYR, which encodes tyrosinase.
Generalized vitiligo is a disease in which patchy depigmentation of skin and hair results from autoimmune loss of melanocytes.
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,
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It is a complex disorder involving multiple susceptibility genes and unknown environmental triggers. Genetic linkage and candidate-gene association studies have implicated several potentially contributory loci, though few have been consistently supported by the data.
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Patients with generalized vitiligo have elevated frequencies of other autoimmune diseases, including autoimmune thyroid disease, rheumatoid arthritis, psoriasis, adult-onset type 1 diabetes, pernicious anemia, systemic lupus erythematosus, and Addison's disease,
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suggesting that these diseases involve shared genetic components. To identify susceptibility loci for generalized vitiligo, we . . . |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 Drs. Jin and Birlea contributed equally to this article. |
ISSN: | 0028-4793 1533-4406 |
DOI: | 10.1056/NEJMoa0908547 |