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      Hair Follicle Melanocytes Initiate Autoimmunity in Alopecia Areata: a Trigger Point

      , ,
      Clinical Reviews in Allergy & Immunology
      Springer Science and Business Media LLC

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          Most cited references132

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          Signal integration in the endoplasmic reticulum unfolded protein response.

          The endoplasmic reticulum (ER) responds to the accumulation of unfolded proteins in its lumen (ER stress) by activating intracellular signal transduction pathways - cumulatively called the unfolded protein response (UPR). Together, at least three mechanistically distinct arms of the UPR regulate the expression of numerous genes that function within the secretory pathway but also affect broad aspects of cell fate and the metabolism of proteins, amino acids and lipids. The arms of the UPR are integrated to provide a response that remodels the secretory apparatus and aligns cellular physiology to the demands imposed by ER stress.
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            Genome-wide association study in alopecia areata implicates both innate and adaptive immunity.

            Alopecia areata (AA) is among the most highly prevalent human autoimmune diseases, leading to disfiguring hair loss due to the collapse of immune privilege of the hair follicle and subsequent autoimmune attack. The genetic basis of AA is largely unknown. We undertook a genome-wide association study (GWAS) in a sample of 1,054 cases and 3,278 controls and identified 139 single nucleotide polymorphisms that are significantly associated with AA (P
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              Alopecia areata

              Alopecia areata is an autoimmune disorder characterized by transient, non-scarring hair loss and preservation of the hair follicle. Hair loss can take many forms ranging from loss in well-defined patches to diffuse or total hair loss, which can affect all hair-bearing sites. Patchy alopecia areata affecting the scalp is the most common type. Alopecia areata affects nearly 2% of the general population at some point during their lifetime. Skin biopsies of affected skin show a lymphocytic infiltrate in and around the bulb or the lower part of the hair follicle in the anagen (hair growth) phase. A breakdown of immune privilege of the hair follicle is thought to be an important driver of alopecia areata. Genetic studies in patients and mouse models have shown that alopecia areata is a complex, polygenic disease. Several genetic susceptibility loci were identified to be associated with signalling pathways that are important to hair follicle cycling and development. Alopecia areata is usually diagnosed based on clinical manifestations, but dermoscopy and histopathology can be helpful. Alopecia areata is difficult to manage medically, but recent advances in understanding the molecular mechanisms have revealed new treatments and the possibility of remission in the near future.
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                Author and article information

                Contributors
                Journal
                Clinical Reviews in Allergy & Immunology
                Clinic Rev Allerg Immunol
                Springer Science and Business Media LLC
                1559-0267
                December 2022
                September 19 2022
                : 63
                : 3
                : 417-430
                Article
                10.1007/s12016-022-08954-w
                36121544
                7c90b352-34d6-4c52-8d4b-85fd3c8f0c22
                © 2022

                https://www.springer.com/tdm

                https://www.springer.com/tdm

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