Innate immune mechanisms in vitiligo: danger from within

被引:204
作者
Richmond, Jillian M. [1 ]
Frisoli, Michael L. [1 ]
Harris, John E. [1 ]
机构
[1] Univ Massachusetts, Sch Med, Dept Med, Div Dermatol, Worcester, MA 01605 USA
基金
美国国家卫生研究院;
关键词
UNFOLDED PROTEIN RESPONSE; T-CELLS; OXIDATIVE STRESS; ENDOPLASMIC-RETICULUM; INCREASED SENSITIVITY; AUTOIMMUNE VITILIGO; CUTTING EDGE; MOUSE MODEL; MELANOCYTES; TYROSINASE;
D O I
10.1016/j.coi.2013.10.010
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
071005 [微生物学]; 100108 [医学免疫学];
摘要
Vitiligo is an autoimmune disease of the skin in which melanocytes are destroyed by antigen-specific T cells, resulting in patchy depigmentation. Although adaptive immunity plays a clear role in disease progression, initiating factors are largely unknown. Many studies report that cellular stress pathways are dysregulated in melanocytes from vitiligo patients, suggesting that melanocyte-intrinsic defects participate in disease pathogenesis. Recent studies reveal that melanocyte stress generates damage-associated molecular patterns that activate innate immunity, thus connecting stress to organ-specific inflammation. Genetic studies in vitiligo support a role for stress, innate immunity, and adaptive mechanisms. Here, we discuss advances in the field that highlight how cellular stress, endogenous danger signals, and innate immune activation promote the onset of vitiligo.
引用
收藏
页码:676 / 682
页数:7
相关论文
共 67 条
[1]
Role of redox potential and reactive oxygen species in stress signaling [J].
Adler, V ;
Yin, ZM ;
Tew, KD ;
Ronai, Z .
ONCOGENE, 1999, 18 (45) :6104-6111
[2]
Vitiligo: A comprehensive overview Part I. Introduction, epidemiology, quality of life, diagnosis, differential diagnosis, associations, histopathology, etiology, and work-up [J].
Alikhan, Ali ;
Felsten, Lesley M. ;
Daly, Meaghan ;
Petronic-Rosic, Vesna .
JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY, 2011, 65 (03) :473-491
[3]
Exosomes: New players in cell-cell communication [J].
Bang, Claudia ;
Thum, Thomas .
INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY, 2012, 44 (11) :2060-2064
[4]
Necrotic but not apoptotic cell death releases heat shock proteins, which deliver a partial maturation signal to dendritic cells and activate the NF-κB pathway [J].
Basu, S ;
Binder, RJ ;
Suto, R ;
Anderson, KM ;
Srivastava, PK .
INTERNATIONAL IMMUNOLOGY, 2000, 12 (11) :1539-1546
[5]
STRUCTURAL-ABERRATION OF THE ROUGH ENDOPLASMIC-RETICULUM AND MELANOSOME COMPARTMENTALIZATION IN LONG-TERM CULTURES OF MELANOCYTES FROM VITILIGO PATIENTS [J].
BOISSY, RE ;
LIU, YY ;
MEDRANO, EE ;
NORDLUND, JJ .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1991, 97 (03) :395-404
[6]
Cutting edge:: Priming of NK cells by IL-18 [J].
Chaix, Julie ;
Tessmer, Marlowe S. ;
Hoebe, Kasper ;
Fuseri, Nicolas ;
Ryffel, Bernhard ;
Dalod, Marc ;
Alexopoulou, Lena ;
Beutler, Bruce ;
Brossay, Laurent ;
Vivier, Eric ;
Walzer, Thierry .
JOURNAL OF IMMUNOLOGY, 2008, 181 (03) :1627-1631
[7]
Sterile inflammation: sensing and reacting to damage [J].
Chen, Grace Y. ;
Nunez, Gabriel .
NATURE REVIEWS IMMUNOLOGY, 2010, 10 (12) :826-837
[8]
Cooper MA, 2001, EUR J IMMUNOL, V31, P792, DOI 10.1002/1521-4141(200103)31:3<792::AID-IMMU792>3.0.CO
[9]
2-U
[10]
N-acetylcysteine protects melanocytes against oxidative stress/damage and delays onset of ultraviolet induced melanoma in mice [J].
Cotter, Murray A. ;
Thomas, Joshua ;
Cassidy, Pamela ;
Robinette, Kyle ;
Jenkins, Noah ;
Florell, Scott R. ;
Leachman, Sancy ;
Samlowski, Wolfram E. ;
Grossman, Douglas .
CLINICAL CANCER RESEARCH, 2007, 13 (19) :5952-5958