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Vitiligo Skin Is Imprinted with Resident Memory CD8 T Cells Expressing CXCR3.

Authors :
Boniface K
Jacquemin C
Darrigade AS
Dessarthe B
Martins C
Boukhedouni N
Vernisse C
Grasseau A
Thiolat D
Rambert J
Lucchese F
Bertolotti A
Ezzedine K
Taieb A
Seneschal J
Source :
The Journal of investigative dermatology [J Invest Dermatol] 2018 Feb; Vol. 138 (2), pp. 355-364. Date of Electronic Publication: 2017 Sep 18.
Publication Year :
2018

Abstract

Vitiligo is a chronic autoimmune depigmenting skin disorder that results from a loss of melanocytes. Multiple combinatorial factors have been involved in disease development, with a prominent role of the immune system, in particular T cells. After repigmentation, vitiligo frequently recurs in the same area, suggesting that vitiligo could involve the presence of resident memory T cells (T <subscript>RM</subscript> ). We sought to perform a thorough characterization of the phenotype and function of skin memory T cells in vitiligo. We show that stable and active vitiligo perilesional skin is enriched with a population of CD8 T <subscript>RM</subscript> expressing both CD69 and CD103 compared with psoriasis and control unaffected skin. CD8 T <subscript>RM</subscript> expressing CD103 are mainly localized in the epidermis. Expression of CXCR3 is observed on most CD8 T <subscript>RM</subscript> in vitiligo, including the population of melanocyte-specific CD8 T cells. CD8 T <subscript>RM</subscript> displayed increased production of IFN-γ and tumor necrosis factor-α with moderate cytotoxic activity. Our study highlights the presence of functional CD8 T <subscript>RM</subscript> in both stable and active vitiligo, reinforcing the concept of vitiligo as an immune memory skin disease. The CD8 T <subscript>RM</subscript> that remain in stable disease could play a role during disease flares, emphasizing the interest in targeting this cell subset in vitiligo.<br /> (Copyright © 2017 The Authors. Published by Elsevier Inc. All rights reserved.)

Details

Language :
English
ISSN :
1523-1747
Volume :
138
Issue :
2
Database :
MEDLINE
Journal :
The Journal of investigative dermatology
Publication Type :
Academic Journal
Accession number :
28927891
Full Text :
https://doi.org/10.1016/j.jid.2017.08.038