Barbara Davis Center for Diabetes, University of Colorado, School of Medicine, Aurora, Colorado.
J Clin Endocrinol Metab. 2018 Oct 1;103(10):3589-3592. doi: 10.1210/jc.2018-01430.
Immune checkpoint inhibitors, including monoclonal antibodies directed against programmed cell death protein 1 (PD-1) and its ligand, have emerged as beneficial cancer immunotherapies. These therapies are known to cause immune-related side effects; however, their role in patients with a preexisting autoimmune disease is not clear.
We describe two cases of anti-PD-1 immune-related adverse events. A 52-year-old male with longstanding type 1 diabetes (T1D), long-term stable kidney transplant, and hypothyroidism received two separate anti-PD-1 monoclonal antibodies for metastatic melanoma. The patient developed acute kidney graft rejection requiring hemodialysis and worsening of autoimmune hypothyroidism 3 weeks after starting treatment. He continued anti-PD-1 treatments and remained on hemodialysis and increased levothyroxine dosage. The second case is a 62-year-old male with no previous history of diabetes who received anti-PD-1 treatment and developed severe diabetic ketoacidosis (DKA) 5 days following the start of therapy. Further laboratory testing revealed high titer antibodies directed against glutamic acid decarboxylase. These antibodies, which were of the IgG isotype and involved in memory immune responses, were likely present before anti-PD-1 treatment. He also had human leukocyte antigen genes that confer T1D genetic risk. Despite normal pretreatment blood glucose levels and HbA1c, the patient requires permanent exogenous insulin treatment.
Patients with preexisting endocrine autoimmunity may have more frequent and severe immune-related side effects with anti-PD-1 treatment. Given the morbidity and mortality associated with solid organ transplant rejection and DKA, clinicians caring for patients receiving these state-of-the-art therapies need to be aware of the potential adverse events.
免疫检查点抑制剂,包括针对程序性细胞死亡蛋白 1(PD-1)及其配体的单克隆抗体,已成为有益的癌症免疫疗法。这些疗法已知会引起免疫相关的副作用;然而,它们在患有预先存在的自身免疫性疾病的患者中的作用尚不清楚。
我们描述了两例抗 PD-1 免疫相关不良事件。一名 52 岁男性患有长期 1 型糖尿病(T1D)、长期稳定的肾移植和甲状腺功能减退症,因转移性黑色素瘤接受了两种单独的抗 PD-1 单克隆抗体治疗。患者在开始治疗后 3 周出现急性肾移植物排斥反应,需要血液透析,自身免疫性甲状腺功能减退症恶化。他继续接受抗 PD-1 治疗,并继续接受血液透析和增加左甲状腺素剂量。第二例是一名 62 岁男性,无糖尿病既往史,接受抗 PD-1 治疗后,在开始治疗后 5 天发生严重糖尿病酮症酸中毒(DKA)。进一步的实验室检测显示针对谷氨酸脱羧酶的高滴度抗体。这些抗体为 IgG 同种型,参与记忆免疫反应,可能在抗 PD-1 治疗之前存在。他还具有赋予 T1D 遗传风险的人类白细胞抗原基因。尽管预处理血糖水平和 HbA1c 正常,但患者需要永久性外源性胰岛素治疗。
患有预先存在的内分泌自身免疫性疾病的患者可能会因抗 PD-1 治疗而出现更频繁和更严重的免疫相关副作用。鉴于实体器官移植排斥和 DKA 相关的发病率和死亡率,接受这些最先进治疗的患者的临床医生需要意识到潜在的不良事件。