Department of Clinical and Environmental Allergology, Jagiellonian University Medical College, Krakow, Poland.
Department of Immunology, Faculty of Biochemistry, Biophysics and Biotechnology, Jagiellonian University, Krakow, Poland.
Front Immunol. 2018 Dec 20;9:3027. doi: 10.3389/fimmu.2018.03027. eCollection 2018.
The human ortholog MRGPRX2 and the mice ortholog, Mrgprb2 are activated by basic secretagogues and neurokinins. A number of commonly used small-molecule drugs (e.g., neuromuscular blocking agents, fluoroquinolones, vancomycin) have been recently shown to activate these receptors under experimental conditions, what results in mast cell degranulation. The above drugs are also known to cause IgE-mediated anaphylactic reactions in allergic patients. The new findings on mechanisms of drug-induced mast cell degranulation may modify the current management of drug hypersensitivity reactions. Clinical interpretation of mild drug-provoked hypersensitivity reactions, interpretation of skin test with a drug of interest or further recommendations for patients suspected of drug allergy are likely to be reconsidered. In the paper we discussed future directions in research on identification and differentiation of MRGPRX2-mediated and IgE-dependent mast cell degranulation in patients presenting clinical features of drug-induced hypersensitivity reactions.
人类同源物 MRGPRX2 和老鼠同源物 Mrgprb2 被碱性分泌素和神经激肽激活。一些常用的小分子药物(如神经肌肉阻滞剂、氟喹诺酮类药物、万古霉素)最近在实验条件下被证明可激活这些受体,导致肥大细胞脱颗粒。这些药物也已知会在过敏患者中引起 IgE 介导的过敏反应。关于药物诱导的肥大细胞脱颗粒的机制的新发现可能会改变目前对药物过敏反应的管理。对轻度药物诱发过敏反应的临床解释、对感兴趣药物的皮肤试验的解释或对疑似药物过敏患者的进一步建议可能需要重新考虑。本文讨论了在表现出药物诱导过敏反应临床特征的患者中鉴定和区分 MRGPRX2 介导和 IgE 依赖性肥大细胞脱颗粒的未来研究方向。