University of Antwerp, Faculty of Medicine and Health Sciences, Department of Immunology, Allergology, Rheumatology and the Infla-Med Centre of Excellence, Antwerp (Belgium) and Immunology, Allergology, Rheumatology, Antwerp University Hospital, Antwerp, Belgium; Department of Immunology and Allergology, AZ Jan Palfijn Gent, Ghent, Belgium.
University of Antwerp, Faculty of Medicine and Health Sciences, Department of Immunology, Allergology, Rheumatology and the Infla-Med Centre of Excellence, Antwerp (Belgium) and Immunology, Allergology, Rheumatology, Antwerp University Hospital, Antwerp, Belgium.
Clin Chim Acta. 2022 Jul 1;532:64-71. doi: 10.1016/j.cca.2022.05.014. Epub 2022 May 21.
The basophil activation test (BAT) has emerged as a reliable complementary diagnostic to document IgE-dependent allergies and to study cross-reactivity between structural homologues. However, the BAT has some weaknesses that hinder a wider application. The BAT requires fresh blood samples and is lost as a diagnostic in patients showing a non-responder status of their cells. The BAT is difficult to standardize mainly because of the difficulty to perform batch analyses. In contrast, mast cell activation tests (MATs), using passively sensitized mast cells (MCs) with patients' sera (henceforth indicated as passive MAT; pMAT), use serum samples that can be frozen, stored, and shipped to a reference center experienced in MC lines and/or cultures and capable of offering batch testing. With the recent recognition of the Mas-related G protein-coupled receptor X2 (MRGPRX2) occupation as a putative mechanism of immediate drug hypersensitivity reactions, the MAT has another advantage compared to the BAT. MCs, in contrast to resting basophils, express the MRGPRX2 and can therefore be used to study this IgE-independent mechanism. This review provides a status update of pMAT in the diagnosis of allergic IgE-mediated hypersensitivity and speculates how direct activation of MCs via the MRGPRX2 receptor could advance paradigms for this non-allergic hypersensitivity.
嗜碱性粒细胞激活试验 (BAT) 已成为一种可靠的辅助诊断方法,可用于记录 IgE 依赖性过敏,并研究结构同源物之间的交叉反应性。然而,BAT 存在一些局限性,限制了其更广泛的应用。BAT 需要新鲜的血液样本,并且在细胞呈无反应状态的患者中失去诊断价值。BAT 难以标准化,主要是因为难以进行批量分析。相比之下,使用患者血清被动致敏的肥大细胞 (MCs) 的肥大细胞激活试验 (MAT)(以下简称被动 MAT;pMAT)可以使用可以冷冻、储存和运送到具有 MC 系和/或培养物经验并能够提供批量测试的参考中心的血清样本。随着最近认识到 Mas 相关 G 蛋白偶联受体 X2 (MRGPRX2) 占据是一种潜在的即时药物过敏反应机制,MAT 与 BAT 相比具有另一个优势。与静止的嗜碱性粒细胞不同,MCs 表达 MRGPRX2,因此可用于研究这种 IgE 非依赖性机制。这篇综述介绍了 pMAT 在诊断 IgE 介导的过敏反应中的最新进展,并推测了通过 MRGPRX2 受体直接激活 MCs 如何为这种非过敏性过敏反应提供新的思路。