Harvard Medical School, Boston, MA, USA.
Department of Dermatology, Brigham and Women's Hospital, Boston, MA, USA.
Clin Exp Dermatol. 2021 Mar;46(2):328-337. doi: 10.1111/ced.14449. Epub 2020 Oct 14.
Immune checkpoint inhibitors (ICI) may cause eruptions resembling cutaneous autoimmune diseases. There are six cases of immunotherapy-associated subacute cutaneous lupus erythematosus (SCLE) in the literature. We present details of five patients referred to the Skin Toxicity Program at the Dana-Farber Cancer Institute/Brigham and Women's Cancer Center who developed de novo immunotherapy-associated SCLE-like eruptions, along with clinicopathological correlation and highlight potential mechanistic features and important diagnostic points. Two patients were maintained on topical corticosteroids, antihistamines and photoprotection. One had complete clearance and two had improvement with addition of hydroxychloroquine. Four patients continued their immunotherapy uninterrupted, while one had immunotherapy suspended for a month before restarting at full dose. Histopathologically, this series illustrates the temporal evolution of ICI-induced immune cutaneous reactions with SCLE subtype. Looking beyond the universally present lichenoid infiltrate, features of evolving SCLE were evident. We hypothesize that programmed death-1 blockade may induce immunological recognition of previously immunologically tolerated drug antigens, leading to epitope spreading and the SCLE phenotype.
免疫检查点抑制剂(ICI)可能会引起类似于皮肤自身免疫性疾病的皮疹。文献中有六例与免疫治疗相关的亚急性皮肤狼疮(SCLE)。我们详细介绍了在达纳-法伯癌症研究所/布莱根妇女癌症中心皮肤毒性计划就诊的五名患者的情况,他们出现了新的免疫治疗相关的 SCLE 样皮疹,并进行了临床病理相关性分析,强调了潜在的机制特征和重要的诊断要点。两名患者接受了局部皮质类固醇、抗组胺药和光保护治疗。一名患者完全缓解,两名患者加用羟氯喹后有所改善。四名患者继续不间断地接受免疫治疗,而一名患者在恢复全剂量治疗前暂停免疫治疗一个月。组织病理学上,本系列说明了 ICI 诱导的免疫性皮肤反应与 SCLE 亚型的时间演变。超越普遍存在的苔藓样浸润,可以明显看出 SCLE 的演变特征。我们假设程序性死亡-1 阻断可能会导致对先前免疫耐受的药物抗原的免疫识别,从而导致表位扩展和出现 SCLE 表型。