Department of Pathology, Johns Hopkins University School of Medicine, Baltimore,MD, USA.
Front Immunol. 2012 Jul 12;3:196. doi: 10.3389/fimmu.2012.00196. eCollection 2012.
The development of type 1 diabetes (T1D) is driven by autoreactive T cells that attack and destroy the insulin-producing β-cells in pancreatic islets, forcing patients to take multiple daily insulin injections. Insulin therapy, however, is not a cure and diabetic patients often develop serious long-term microvascular and cardiovascular complications. Therefore, intensive efforts are being directed toward developing safe immunotherapy for the disease that does not impair host defense and preserves β-cells, leading to better glycemic control than exogenous insulin therapy. Engineering therapies that differentially cripple or tolerate autoreactive diabetogenic T cells while sparing protective T cells necessary for maintaining a competent immune system has proven challenging. Instead, recent efforts have focused on modulating or resetting the immune system through global but transient deletion of T cells or B cells using anti-CD3 or anti-CD20 mAb, respectively. However, phase III clinical trials have shown promising but modest efficacy so far with these approaches. Therefore, there is a need to identify novel biological targets that do not fit the classic properties of being involved in adaptive immune cell activation. In this prospective, we provide preclinical evidence that targeting Fas ligand (FasL) may provide a unique opportunity to prevent or cure T1D and perhaps other organ-specific autoimmune diseases without causing immune suppression. Unlike conventional targets that are involved in T and B lymphocyte activation (such as CD3 and CD20, respectively), FasL is an apoptosis-inducing surface molecule that triggers cell death by binding to Fas (also known as CD95 Apo-1). Therefore, targeting FasL is not expected to cause immune suppression, the Achilles Heel of conventional approaches. We will discuss the hypothesis that targeting FasL has unique benefits that are not offered by current immunomodulatory approaches.
1 型糖尿病(T1D)的发展是由自身反应性 T 细胞驱动的,这些细胞攻击并破坏胰腺胰岛中的胰岛素产生β细胞,迫使患者每天多次注射胰岛素。然而,胰岛素治疗不是一种治愈方法,糖尿病患者经常会出现严重的长期微血管和心血管并发症。因此,人们正在积极努力开发安全的免疫疗法,这种疗法不会损害宿主防御并保留β细胞,从而比外源性胰岛素治疗更好地控制血糖。工程疗法旨在使自身反应性致糖尿病 T 细胞失能或耐受,同时保留维持免疫系统功能所需的保护性 T 细胞,但事实证明这具有挑战性。相反,最近的努力集中在通过使用抗 CD3 或抗 CD20 mAb 分别对 T 细胞或 B 细胞进行全球但短暂的删除来调节或重置免疫系统。然而,到目前为止,这些方法的 III 期临床试验显示出有希望但疗效中等。因此,需要确定新的生物学靶点,这些靶点不符合参与适应性免疫细胞激活的经典特性。在本前瞻性研究中,我们提供了临床前证据,表明靶向 Fas 配体(FasL)可能为预防或治愈 T1D 以及其他可能的器官特异性自身免疫性疾病提供独特的机会,而不会引起免疫抑制。与参与 T 和 B 淋巴细胞激活的传统靶点(分别为 CD3 和 CD20)不同,FasL 是一种凋亡诱导表面分子,通过与 Fas(也称为 CD95 Apo-1)结合触发细胞死亡。因此,靶向 FasL 预计不会引起免疫抑制,这是传统方法的阿喀琉斯之踵。我们将讨论这样一个假设,即靶向 FasL 具有当前免疫调节方法所不具备的独特益处。