International Collaboration On Repair Discoveries (ICORD), Vancouver Coastal Health Research Institute (VCHRI), Vancouver, BC, Canada.
Department of Pathology and Laboratory Medicine, University of British Columbia (UBC), Vancouver, BC, Canada.
Front Immunol. 2019 Jun 26;10:1454. doi: 10.3389/fimmu.2019.01454. eCollection 2019.
Pemphigoid diseases are a subgroup of autoimmune skin diseases characterized by widespread tense blisters. Standard of care typically involves immunosuppressive treatments, which may be insufficient and are often associated with significant adverse events. As such, a deeper understanding of the pathomechanism(s) of pemphigoid diseases is necessary in order to identify improved therapeutic approaches. A major initiator of pemphigoid diseases is the accumulation of autoantibodies against proteins at the dermal-epidermal junction (DEJ), followed by protease activation at the lesion. The contribution of proteases to pemphigoid disease pathogenesis has been investigated using a combination of and models. These studies suggest proteolytic degradation of anchoring proteins proximal to the DEJ is crucial for dermal-epidermal separation and blister formation. In addition, proteases can also augment inflammation, expose autoantigenic cryptic epitopes, and/or provoke autoantigen spreading, which are all important in pemphigoid disease pathology. The present review summarizes and critically evaluates the current understanding with respect to the role of proteases in pemphigoid diseases.
天疱疮病是一种自身免疫性皮肤病,其特征是广泛出现紧张性水疱。标准治疗方法通常包括免疫抑制治疗,但这种方法可能并不充分,而且常伴有严重的不良反应。因此,为了确定改进的治疗方法,有必要深入了解天疱疮病的发病机制。天疱疮病的一个主要启动因素是在表皮-真皮交界处(DEJ)积聚针对蛋白质的自身抗体,随后在病变部位激活蛋白酶。已经使用 和 模型组合来研究蛋白酶在天疱疮病发病机制中的作用。这些研究表明,靠近 DEJ 的锚定蛋白的蛋白水解降解对于真皮-表皮分离和水疱形成至关重要。此外,蛋白酶还可以增强炎症、暴露自身抗原的隐匿表位,和/或引发自身抗原扩散,这些在天疱疮病病理中都很重要。本文综述总结并批判性评估了目前对蛋白酶在天疱疮病中的作用的理解。