Targeting the PD-1/PD-L1 Axis in Human Vitiligo

被引:14
|
作者
Willemsen, Marcella [1 ,2 ]
Melief, Cornelis J. M. [3 ]
Bekkenk, Marcel W. [1 ,2 ]
Luiten, Rosalie M. [1 ,2 ]
机构
[1] Univ Amsterdam, Amsterdam Univ Med Ctr, Canc Ctr Amsterdam,Dept Dermatol, Amsterdam Infect & Immun Inst,Locat AMC, Amsterdam, Netherlands
[2] Univ Amsterdam, Amsterdam Univ Med Ctr, Canc Ctr Amsterdam,Netherlands Inst Pigment Disor, Amsterdam Infect & Immun Inst,Locat AMC, Amsterdam, Netherlands
[3] ISA Pharmaceut, Leiden, Netherlands
来源
FRONTIERS IN IMMUNOLOGY | 2020年 / 11卷
关键词
vitiligo; programmed cell death 1 receptor; B7-H1; antigen; immune tolerance; autoimmunity; NONMELANOMA SKIN-CANCER; REGULATORY T-CELLS; STAGE-III; MELANOMA; AUTOIMMUNITY; PD-L1; EXPRESSION; NIVOLUMAB; RESPONSES; BLOCKADE;
D O I
10.3389/fimmu.2020.579022
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Autoreactive CD8(+) T cells play a pivotal role in melanocyte destruction in autoimmune vitiligo. Immunotherapy for melanoma often leads to autoimmune side-effects, among which vitiligo-like depigmentation, indicating that targeting immune checkpoints can break peripheral tolerance against self-antigens in the skin. Therapeutically enhancing immune checkpoint signaling by immune cells or skin cells, making self-reactive T cells anergic, seems a promising therapeutic option for vitiligo. Here, we review the current knowledge on the PD-1/PD-L1 pathway in vitiligo as new therapeutic target for vitiligo therapy.
引用
收藏
页数:7
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