Department of Gastroenterology, Hepatology and Endocrinology, Hannover Medical School, Hannover, Germany.
Department of Gastroenterology, Hepatology and Endocrinology, Hannover Medical School, Hannover, Germany; German Centre for Infection Research (DZIF), Partner Site Hannover-Braunschweig, Germany; Helmholtz Centre for Infection Research (HZI), Braunschweig, Germany.
J Autoimmun. 2018 Dec;95:34-46. doi: 10.1016/j.jaut.2018.10.022. Epub 2018 Nov 4.
Autoimmune hepatitis (AIH) is an orphan disease characterized by an autoimmune attack against hepatocytes. The exact sequence of events that leads to a breach of tolerance is incompletely understood. Current hypotheses suggest that environmental agents such as toxins or infectious agents like viruses cause a tissue damage that initiates autoimmunity in genetically susceptible individuals. The growing knowledge of the multi-facetted immune dysregulation, which involves Th1/Th17 polarization and the suspected inability of regulatory T cells to revert autoimmunity in the otherwise tolerogenic milieu of the liver, offers multiple new therapeutic approaches and targets. Standard of care (SOC) is treatment with corticosteroids with or without azathioprine, which is sufficient to induce remission in the majority of patients. However, it rarely cures AIH or restores intrahepatic immune tolerance. Hence, life-long therapy is required in the majority of patients. In addition, several studies suggest a weakening of immune regulation mediated by intrahepatic T cells under current therapies. Furthermore, second line therapies for non-responders, intolerant or otherwise difficult to treat patients are urgently needed as this is relevant for at least one fifth of all patients with inefficacy or intolerance to SOC. Current second line therapies are mainly based on single center retrospective experiences and none of them have been approved by regulatory authorities for AIH, yet. This article highlights new therapeutic approaches based on our growing knowledge on the pathophysiology of AIH. It focuses on cell-based therapies that strengthen or restore immune tolerance. An additional focus lies on new therapeutic agents showing promising results in non-hepatic autoimmune diseases that have a potential for treating AIH. The dynamics in the whole field of innovative therapies for non-hepatic autoimmune diseases will hopefully improve the therapeutic armamentarium for AIH patients in the future.
自身免疫性肝炎(AIH)是一种孤儿病,其特征是针对肝细胞的自身免疫攻击。导致耐受破裂的确切事件序列尚不完全清楚。目前的假设表明,环境因素(如毒素)或传染性因素(如病毒)会导致组织损伤,从而使遗传易感个体产生自身免疫。对多方面免疫失调的认识不断提高,其中包括 Th1/Th17 极化,以及调节性 T 细胞在肝脏这种本来具有免疫耐受的环境中无法逆转自身免疫的可能性,为多种新的治疗方法和靶点提供了依据。标准治疗(SOC)是使用皮质类固醇加或不加硫唑嘌呤治疗,这足以使大多数患者缓解。然而,它很少能治愈 AIH 或恢复肝内免疫耐受。因此,大多数患者需要终身治疗。此外,几项研究表明,当前的治疗方法削弱了肝内 T 细胞介导的免疫调节。此外,对于无应答者、不耐受或其他难以治疗的患者,迫切需要二线治疗方法,因为这与 SOC 无效或不耐受的至少五分之一患者有关。目前的二线治疗方法主要基于单中心回顾性经验,并且尚未有任何一种方法获得监管机构批准用于 AIH。本文基于我们对 AIH 病理生理学的日益了解,重点介绍了新的治疗方法。它侧重于增强或恢复免疫耐受的基于细胞的治疗方法。另外,重点关注在非肝脏自身免疫性疾病中显示出有前途结果的新型治疗药物,这些药物有可能治疗 AIH。非肝脏自身免疫性疾病创新治疗领域的动态有望在未来改善 AIH 患者的治疗手段。