Understanding autoimmunity of vitiligo and alopecia areata. Issue 4 (August 2016)
- Record Type:
- Journal Article
- Title:
- Understanding autoimmunity of vitiligo and alopecia areata. Issue 4 (August 2016)
- Main Title:
- Understanding autoimmunity of vitiligo and alopecia areata
- Authors:
- Rork, Jillian F.
Rashighi, Mehdi
Harris, John E. - Abstract:
- Abstract : Purpose of review: Vitiligo and alopecia areata are common, disfiguring skin diseases. Treatment options are limited and include nontargeted approaches, such as corticosteroids, topical calcineurin inhibitors, narrow band ultraviolet B phototherapy, and other immune-modifying agents. The purpose of this article is to review shared, novel mechanisms between vitiligo and alopecia areata, as well as discuss how they inform the development of future targeted treatments. Recent findings: Vitiligo and alopecia areata are both autoimmune diseases, and striking similarities in pathogenesis have been identified at the level of both the innate and adaptive immune system. Increased reactive oxygen species and high cellular stress level have been suggested as the initiating trigger of the innate immune system in both diseases, and genome-wide association studies have implicated risk alleles that influence both innate and adaptive immunity. Most importantly, mechanistic studies in mouse models of vitiligo and alopecia areata have specifically implicated an interferon (IFN)γ-driven immune response, including IFNγ, IFNγ-induced chemokines, and cytotoxic CD8 + T cells as the main drivers of disease pathogenesis. These recent discoveries may reveal an effective strategy to develop new treatments, and several proof-of-concept clinical studies support this hypothesis. Summary: The identification of IFNγ-driven immune signaling pathways has enabled discoveries of potential newAbstract : Purpose of review: Vitiligo and alopecia areata are common, disfiguring skin diseases. Treatment options are limited and include nontargeted approaches, such as corticosteroids, topical calcineurin inhibitors, narrow band ultraviolet B phototherapy, and other immune-modifying agents. The purpose of this article is to review shared, novel mechanisms between vitiligo and alopecia areata, as well as discuss how they inform the development of future targeted treatments. Recent findings: Vitiligo and alopecia areata are both autoimmune diseases, and striking similarities in pathogenesis have been identified at the level of both the innate and adaptive immune system. Increased reactive oxygen species and high cellular stress level have been suggested as the initiating trigger of the innate immune system in both diseases, and genome-wide association studies have implicated risk alleles that influence both innate and adaptive immunity. Most importantly, mechanistic studies in mouse models of vitiligo and alopecia areata have specifically implicated an interferon (IFN)γ-driven immune response, including IFNγ, IFNγ-induced chemokines, and cytotoxic CD8 + T cells as the main drivers of disease pathogenesis. These recent discoveries may reveal an effective strategy to develop new treatments, and several proof-of-concept clinical studies support this hypothesis. Summary: The identification of IFNγ-driven immune signaling pathways has enabled discoveries of potential new treatments for vitiligo and alopecia areata, and supports initiation of larger clinical trials. … (more)
- Is Part Of:
- Current opinion in pediatrics. Volume 28:Issue 4(2016:Aug.)
- Journal:
- Current opinion in pediatrics
- Issue:
- Volume 28:Issue 4(2016:Aug.)
- Issue Display:
- Volume 28, Issue 4 (2016)
- Year:
- 2016
- Volume:
- 28
- Issue:
- 4
- Issue Sort Value:
- 2016-0028-0004-0000
- Page Start:
- Page End:
- Publication Date:
- 2016-08
- Subjects:
- alopecia areata -- autoimmune -- interferonγ -- Janus kinase -- vitiligo
Pediatrics -- Periodicals
Pediatrics -- Periodicals -- Bibliography -- Periodicals
618.92 - Journal URLs:
- http://journals.lww.com/co-pediatrics/pages/default.aspx ↗
http://journals.lww.com/pages/default.aspx ↗ - DOI:
- 10.1097/MOP.0000000000000375 ↗
- Languages:
- English
- ISSNs:
- 1040-8703
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3500.776800
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 14502.xml