Expression of programmed cell death ligand 1 and programmed cell death 1 in cutaneous warts

被引:4
作者
Yu, Wesley Y. [1 ]
Berger, Timothy G. [1 ]
North, Jeffrey P. [1 ,2 ]
Laszik, Zoltan [2 ]
Cohen, Jarish N. [1 ,2 ]
机构
[1] Univ Calif San Francisco, Dept Dermatol, San Francisco, CA 94143 USA
[2] Univ Calif San Francisco, Dept Pathol, San Francisco, CA 94140 USA
关键词
HPV; human papillomavirus; immunotherapy; interface dermatitis; pathophysiology; PD-1; virology; warts; PD-L1; EXPRESSION; ASSOCIATION; INFECTION; CANCER;
D O I
10.1016/j.jaad.2019.02.063
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Background: Cutaneous warts have high prevalence and cause significant morbidity. Understanding the mechanisms by which warts evade the immune system could lead to targeted and improved treatments. Objective: To determine whether cutaneous warts express programmed cell death ligand 1 (PD-L1) and to characterize the expression of programmed cell death 1 (PD-1) within the immune infiltrate of inflamed lesions. Methods: In total, 44 biopsies of cutaneous warts were retrieved from the Department of Dermatopathology archives of the University of California, San Francisco. Biopsies were stained with hematoxylin and eosin and PD-L1 monoclonal antibody, and biopsies of inflamed lesions were stained with PD-1 monoclonal antibody. Results: PD-L1 was expressed on keratinocytes in cases of verrucae vulgares (12/30, 40%) and myrmecia (7/14, 50%) and was associated with an interface inflammatory reaction. PD-1 was expressed by the inflammatory infiltrate in verrucae vulgares (21/24, 88%) and myrmecia (5/8, 63%). Limitations: This was a retrospective observational study conducted at a single institution. Conclusion: Many cutaneous warts express PD-L1, suggesting that human papillomavirus might use this pathway to promote immune dysfunction. This discovery helps explain the recalcitrance of warts to current therapies and provides a rationale for investigating antiePD-1 immunotherapy as a potential treatment for warts.
引用
收藏
页码:1127 / 1133
页数:7
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