Kittai Adam S, Oldham Hayden, Cetnar Jeremy, Taylor Matthew
Departments of *Hematology and Medical Oncology†Internal Medicine, Oregon Health & Science University, Portland, OR.
J Immunother. 2017 Sep;40(7):277-281. doi: 10.1097/CJI.0000000000000180.
Modulation of T-cell activity through blockade of coinhibitory molecules has revolutionized the treatment of various malignancies. Several immune checkpoint inhibitors are currently Food and Drug Administration approved which target various coinhibitory pathways including cytotoxic T-lymphocyte-associated protein 4 (CTLA-4), programmed death 1 receptor (PD-1), and programmed cell death ligand-1. Clinical trials that lead to the Food and Drug Administration approval of these agents often excluded patients with an organ transplant. Excluding these patients was deliberate due to concern that immune checkpoint inhibitor therapy could lead to graft rejection. The PD-1 and CTLA-4 pathways are essential to downregulate our immune system in the setting of T-cell activation to prevent autoimmunity. Furthermore, both pathways are implicated in transplanted organ tolerance and modulation of the pathways may inadvertently lead to peripheral transplant rejection. Currently, there are no guidelines for the treatment of patients with immune checkpoint inhibitors in the setting of a prior organ transplant. Thus far, there are only 10 reported cases of patients in the literature who were treated in this setting. Two additional cases are reported herein, including 1 patient with a prior cardiac transplant receiving nivolumab for non-small cell lung cancer. Of the 12 cases, 4 patients experienced organ rejection. From these observations, the authors hypothesize factors that affect safety and of this treatment modality in this patient population. These factors include the integral role of the PD-1 pathway compared with the CTLA-4 pathway in organ acceptance, sequential implementation of different immune checkpoint inhibitor classes, length of time with a transplant before therapy, strength of immunosuppressive agents to prevent organ transplant rejection, and immunogenicity of the particular organ grafted. Although limited cases have been reported, there are circumstances in which immune checkpoint inhibitors have been used in the setting of organ transplantation without resulting in organ rejection. A thorough discussion with the patient of the potential risks, including graft rejection, and benefits of this therapy is necessary before beginning this treatment. More research is needed to explore the safety and efficacy of immune checkpoint inhibitors in the setting of organ transplantation.
通过阻断共抑制分子来调节T细胞活性,彻底改变了各种恶性肿瘤的治疗方式。目前,有几种免疫检查点抑制剂已获得美国食品药品监督管理局(FDA)的批准,它们靶向多种共抑制途径,包括细胞毒性T淋巴细胞相关蛋白4(CTLA-4)、程序性死亡1受体(PD-1)和程序性细胞死亡配体1。导致这些药物获得FDA批准的临床试验通常将器官移植患者排除在外。排除这些患者是出于对免疫检查点抑制剂疗法可能导致移植排斥反应的担忧。在T细胞激活的情况下,PD-1和CTLA-4途径对于下调我们的免疫系统以预防自身免疫至关重要。此外,这两条途径都与移植器官的耐受性有关,调节这些途径可能会无意中导致外周移植排斥反应。目前,对于曾接受过器官移植的患者使用免疫检查点抑制剂进行治疗尚无指导原则。到目前为止,文献中仅报道了10例在此情况下接受治疗的患者。本文报告另外2例,包括1例曾接受心脏移植的患者接受纳武单抗治疗非小细胞肺癌。在这12例病例中,4例患者发生了器官排斥反应。基于这些观察结果,作者推测了影响该患者群体中这种治疗方式安全性的因素。这些因素包括与CTLA-4途径相比,PD-1途径在器官接受方面的不可或缺作用、不同类别的免疫检查点抑制剂的序贯应用、治疗前移植的时间长度、预防器官移植排斥反应的免疫抑制剂的强度以及所移植特定器官的免疫原性。尽管报道的病例有限,但在某些情况下,免疫检查点抑制剂已用于器官移植环境中而未导致器官排斥反应。在开始这种治疗之前,有必要与患者充分讨论潜在风险,包括移植排斥反应,以及这种疗法的益处。需要更多研究来探索免疫检查点抑制剂在器官移植环境中的安全性和有效性。