2010
DOI: 10.1155/2010/928030
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Cytokines and Other Mediators in Alopecia Areata

Abstract: Alopecia areata, a disease of the hair follicles with multifactorial etiology and a strong component of autoimmune origin, has been extensively studied as far as the role of several cytokines is concerned. So far, IFN-γ, interleukins, TNF-α, are cytokines that are well known to play a major role in the pathogenesis of the disease, while several studies have shown that many more pathways exist. Among them, MIG, IP-10, BAFF, HLA antigens, MIG, as well as stress hormones are implicated in disease onset and activi… Show more

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Cited by 116 publications
(118 citation statements)
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“…MHC class I is strongly expressed in AA lesions, along with MHC II. Classical upregulators of MHC I expression like interferon (IFN)-γ [31], tumor necrosis factor (TNF)-α, and interleukin (IL)-1β [63] are enhanced in AA lesions and down-modulators of MHC I expression (IL-10, αMSH, IGF-1, TGFβ) are modified in AA lesions as well [18,31,64]. Specific genetic polymorphisms of HLA-DQB1 and HLA-DRB1, which belong to the HLA class II beta chain paralogs, strongly correlate to increased probability of AA onset [65][66][67].…”
Section: Immune Privilege Collapse In Alopecia Areatamentioning
confidence: 99%
“…MHC class I is strongly expressed in AA lesions, along with MHC II. Classical upregulators of MHC I expression like interferon (IFN)-γ [31], tumor necrosis factor (TNF)-α, and interleukin (IL)-1β [63] are enhanced in AA lesions and down-modulators of MHC I expression (IL-10, αMSH, IGF-1, TGFβ) are modified in AA lesions as well [18,31,64]. Specific genetic polymorphisms of HLA-DQB1 and HLA-DRB1, which belong to the HLA class II beta chain paralogs, strongly correlate to increased probability of AA onset [65][66][67].…”
Section: Immune Privilege Collapse In Alopecia Areatamentioning
confidence: 99%
“…TNF, although discovered as a result of its antitumor activity in the beginning, has now been found having functions in tumor initiation, progression, and metastasis [28]. TNF-α, synthesized in epidermal keratinocytes was shown to be a very potent inhibitor of follicle proliferation and plays a major role in the pathogenesis of alopecia areata (AA) [29]. Intradermal injection of TNF-α caused a significant high number of apoptotic cells in the epidermis [30].…”
Section: Gene Expression Analysis (Real-time Qpcr)mentioning
confidence: 99%
“…Akut emosyonel stres, olas›l›kla k›l folikülleri etraf›nda yerleflmifl olan Tip 2 β kortikotropin serbestlefltirici hormon reseptörleri-ni aktive ederek yo¤un lokal enflamasyona ve saç dökülmesi-ne yol açmaktad›r 28 . Ayr›ca alopesi areata (AA) alan›ndaki k›l folikülleri etraf›nda Substans P (SP)'nin belirgin olarak artt›¤› ve bunun strese yan›t olarak periferik sinir uçlar›ndan salg›lan-d›¤› bildirilmektedir [28][29] . Bu moleküler araflt›rmalar AA'l› hastalarda stres hormonlar›n›n enflamasyon üzerinde etkili oldu¤u-nu düflündürürken baz› araflt›rmac›lar stresin o denli etkin olmad›¤›n› ileri sürmektedir.…”
Section: Alopesi Areataunclassified