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肿瘤坏死因子-α在抗磷脂综合征中的有害作用,以及生物制药诱导的抗磷脂抗体的从头合成。

Detrimental roles of TNF-alpha in the antiphospholipid syndrome and de novo synthesis of antiphospholipid antibodies induced by biopharmaceuticals against TNF-alpha.

机构信息

Faculty of Medicine, Department of Pharmacy, University of Novi Sad, Hajduk Veljkova 3, Novi Sad, 21000, Serbia.

出版信息

J Thromb Thrombolysis. 2017 Nov;44(4):565-570. doi: 10.1007/s11239-017-1571-4.

Abstract

Antiphospholipid syndrome (APS) is an autoimmune disease that is characterized by arterial and/or venous thrombosis and/or recurrent pregnancy losses. Obstetric APS (OAPS) is considered as a distinct entity from vascular APS (VAPS). In the absence of any additional disease, APS is designated as primary (PAPS), while the term secondary APS (SAPS) is used when other diseases are associated. Catastrophic APS (CAPS) is characterized by the rapid development of multiple thrombosis in various vital organs. The presence of antiphospholipid antibodies (aPL Abs) is considered as a laboratory criterion for APS diagnosis. aPL Abs cause an increase in systemic and decidual TNF-alpha levels in experimental model of APS (eAPS), while paradoxically, administration of TNF-alpha blockers has been associated with de novo synthesis of aPL Abs in patients with various autoimmune diseases. While eAPS provides evidence for the fact that application of TNF-alpha blockers has beneficial effects, lack of randomized prospective studies is the main obstacle for consideration of TNF-alpha blockers administration as a therapeutic option not for all, but at least for selected cases of APS patients despite compelling evidence for detrimental roles of TNF-alpha for both VASP and OAPS. This article represents a review of previously published reports on detrimental roles of TNF-alpha in APS, reports on the application of anti-TNF-alpha agents in eAPS and articles that reported de novo synthesis of aPL Abs induced by biopharmaceuticals against TNF-alpha.

摘要

抗磷脂综合征(APS)是一种自身免疫性疾病,其特征为动脉和/或静脉血栓形成和/或复发性妊娠丢失。产科 APS(OAPS)被认为是与血管 APS(VAPS)不同的实体。在没有任何其他疾病的情况下,APS 被指定为原发性(PAPS),而当存在其他疾病时,则使用术语继发性 APS(SAPS)。灾难性 APS(CAPS)的特征为多种血栓在各种重要器官中迅速发展。抗磷脂抗体(aPL Abs)的存在被认为是 APS 诊断的实验室标准。aPL Abs 在 APS 的实验模型(eAPS)中导致全身性和蜕膜 TNF-α水平升高,而矛盾的是,TNF-α 阻滞剂的给药与各种自身免疫性疾病患者中 aPL Abs 的从头合成有关。虽然 eAPS 提供了 TNF-α 阻滞剂应用具有有益效果的证据,但缺乏随机前瞻性研究是将 TNF-α 阻滞剂给药作为治疗选择考虑的主要障碍,不仅对所有 APS 患者,而且至少对选定的 APS 患者,尽管 TNF-α 对 VASP 和 OAPS 都有有害作用的证据确凿。本文综述了先前发表的关于 TNF-α 在 APS 中的有害作用的报告、关于在 eAPS 中应用抗 TNF-α 药物的报告以及报告生物制药诱导的 TNF-α 诱导的 aPL Abs 从头合成的文章。

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