Department of Pathology and Medical Biology, University of Groningen, University Medical Center Groningen, Groningen, Netherlands.
Department of Rheumatology and Clinical Immunology, University of Groningen, University Medical Center Groningen, Groningen, Netherlands.
Front Immunol. 2018 Feb 22;9:315. doi: 10.3389/fimmu.2018.00315. eCollection 2018.
Age-associated changes in the immune system including alterations in surface protein expression are thought to contribute to an increased susceptibility for autoimmune diseases. The balance between the expression of coinhibitory and costimulatory surface protein molecules, also known as immune checkpoint molecules, is crucial in fine-tuning the immune response and preventing autoimmunity. The activation of specific inhibitory signaling pathways allows cancer cells to evade recognition and destruction by the host immune system. The use of immune checkpoint inhibitors (ICIs) to treat cancer has proven to be effective producing durable antitumor responses in multiple cancer types. However, one of the disadvantages derived from the use of these agents is the appearance of inflammatory manifestations termed immune-related adverse events (irAEs). These irAEs are often relatively mild, but more severe irAEs have been reported as well including several forms of vasculitis. In this article, we argue that age-related changes in expression and function of immune checkpoint molecules lead to an unstable immune system, which is prone to tolerance failure and autoimmune vasculitis development. The topic is introduced by a case report from our hospital describing a melanoma patient treated with ICIs and who subsequently developed biopsy-proven giant cell arteritis. Following this case report, we present an in-depth review on the role of immune checkpoint pathways in the development and progression of autoimmune vasculitis and its relation with an aging immune system.
随着年龄的增长,免疫系统会发生变化,包括表面蛋白表达的改变,这被认为是导致自身免疫性疾病易感性增加的原因之一。共抑制和共刺激表面蛋白分子(也称为免疫检查点分子)的表达平衡对于微调免疫反应和预防自身免疫至关重要。特定抑制性信号通路的激活使癌细胞能够逃避宿主免疫系统的识别和破坏。使用免疫检查点抑制剂(ICIs)治疗癌症已被证明是有效的,可在多种癌症类型中产生持久的抗肿瘤反应。然而,使用这些药物的一个缺点是出现了称为免疫相关不良事件(irAEs)的炎症表现。这些 irAEs 通常相对较轻,但也有更严重的 irAEs 报告,包括几种血管炎形式。在本文中,我们认为免疫检查点分子表达和功能的年龄相关变化导致免疫系统不稳定,容易发生耐受失败和自身免疫性血管炎的发展。该主题由我们医院的一个病例报告引入,该报告描述了一名接受 ICI 治疗的黑色素瘤患者,随后发展为经活检证实的巨细胞性动脉炎。在这个病例报告之后,我们对免疫检查点途径在自身免疫性血管炎的发展和进展中的作用及其与衰老免疫系统的关系进行了深入的综述。