Buyansky Dimitry, Fallaha Catherine, Gougeon François, Pépin Marie-Noëlle, Cailhier Jean-François, Beaubien-Souligny William
Université de Montréal, Québec, Canada.
Department of Pathology, Centre Hospitalier de l'Université de Montréal, Québec, Canada.
Can J Kidney Health Dis. 2021 May 19;8:20543581211014745. doi: 10.1177/20543581211014745. eCollection 2021.
Immune checkpoint inhibitors are monoclonal antibodies used in the treatment of various types of cancers. The downside of using such molecules is the potential risk of developing immune-related adverse events. Factors that trigger these autoimmune side effects are yet to be elucidated. Although any organ can potentially be affected, kidney involvement is usually rare. In this case report, we describe the first known instance of a patient being treated with an inhibitor of programmed death-ligand 1 (anti-PD-L1, a checkpoint inhibitor) who develops acute tubulointerstitial nephritis after contracting the severe acute respiratory syndrome coronavirus 2.
A 62-year-old patient, on immunotherapy treatment for stage 4 squamous cell carcinoma, presents to the emergency department with symptoms of lower respiratory tract infection. Severe acute kidney injury is discovered with electrolyte imbalances requiring urgent dialysis initiation. Further testing reveals that the patient has contracted the severe acute respiratory syndrome coronavirus 2.
A kidney biopsy was performed and was compatible with acute tubulointerstitial nephritis.
The patient was treated with high dose corticosteroid therapy followed by progressive tapering.
Rapid and sustained normalization of kidney function was achieved after completion of the steroid course.
We hypothesize that the viral infection along with checkpoint inhibitor use has created a proinflammatory environment which led to a loss of self-tolerance to renal parenchyma. Viruses may play a more important role in the pathogenesis of autoimmunity in this patient population than was previously thought.
免疫检查点抑制剂是用于治疗各种类型癌症的单克隆抗体。使用此类分子的缺点是存在发生免疫相关不良事件的潜在风险。引发这些自身免疫副作用的因素尚待阐明。尽管任何器官都可能受到潜在影响,但肾脏受累通常很少见。在本病例报告中,我们描述了首例已知的在用程序性死亡配体1抑制剂(抗PD-L1,一种检查点抑制剂)治疗的患者中,在感染严重急性呼吸综合征冠状病毒2后发生急性肾小管间质性肾炎的情况。
一名62岁的患者,正在接受针对4期鳞状细胞癌的免疫治疗,因下呼吸道感染症状到急诊科就诊。发现严重急性肾损伤并伴有电解质失衡,需要紧急开始透析。进一步检查显示该患者感染了严重急性呼吸综合征冠状病毒2。
进行了肾活检,结果与急性肾小管间质性肾炎相符。
患者接受了高剂量皮质类固醇治疗,随后逐渐减量。
类固醇疗程结束后,肾功能迅速且持续恢复正常。
我们推测病毒感染与检查点抑制剂的使用共同营造了一种促炎环境,导致对肾实质的自身耐受性丧失。在该患者群体中,病毒在自身免疫发病机制中可能发挥比先前认为的更重要的作用。