Chan Yih-Chih, Ramadani Faruk, Santos Alexandra F, Pillai Prathap, Ohm-Laursen Line, Harper Clare E, Fang Cailong, Dodev Tihomir S, Wu Shih-Ying, Ying Sun, Corrigan Christopher J, Gould Hannah J
Department of Asthma, Allergy and Respiratory Science and Randall Division of Cell and Molecular Biophysics, King's College London; the Medical Research Council and Asthma UK Centre, Allergic Mechanisms in Asthma, London; the Department of Paediatric Allergy, Guy's and St Thomas' National Health Service Foundation Trust, London, United Kingdom.
Department of Asthma, Allergy and Respiratory Science and Randall Division of Cell and Molecular Biophysics, King's College London; the Medical Research Council and Asthma UK Centre, Allergic Mechanisms in Asthma, London; the Department of Paediatric Allergy, Guy's and St Thomas' National Health Service Foundation Trust, London, United Kingdom; Immunoallergology Department, Coimbra University Hospital, Coimbra, Portugal.
J Allergy Clin Immunol. 2014 Dec;134(6):1394-1401.e4. doi: 10.1016/j.jaci.2014.06.029. Epub 2014 Aug 10.
Naturally occurring IgE-specific IgG autoantibodies have been identified in patients with asthma and other diseases, but their spectrum of functions is poorly understood.
Address the hypothesis that: (i) IgG anti-IgE autoantibodies are detectable in the serum of all subjects but elevated in asthmatic patients regardless of atopic status as compared with controls; (ii) some activate IgE-sensitized basophils; and (iii) some inhibit allergen-induced basophil activation.
IgE-specific IgG autoantibodies were detected and quantified in sera using ELISA. Sera were examined for their ability to activate IgE-sensitized human blood basophils in the presence and absence of allergen using a basophil activation test, and to inhibit allergen binding to specific IgE on a rat basophilic cell line stably expressing human FcεRI.
IgG autoantibodies binding to both free and FcεRI-bound IgE were detected in patients with atopic and non-atopic asthma, as well as controls. While some were able to activate IgE-sensitised basophils, others inhibited allergen-induced basophil activation, at least partly by inhibiting binding of IgE to specific allergen.
Naturally occurring IgG anti-IgE autoantibodies may inhibit, as well as induce, basophil activation. They act in a manner distinct from therapeutic IgG anti-IgE antibodies such as omalizumab. They may at least partly explain why atopic subjects who make allergen-specific IgE never develop clinical symptoms, and why omalizumab therapy is of variable clinical benefit in severe atopic asthma.
在哮喘患者和其他疾病患者中已鉴定出天然存在的IgE特异性IgG自身抗体,但其功能谱尚不清楚。
验证以下假设:(i)所有受试者血清中均可检测到IgG抗IgE自身抗体,但与对照组相比,无论特应性状态如何,哮喘患者体内该抗体水平均升高;(ii)某些IgG抗IgE自身抗体可激活IgE致敏的嗜碱性粒细胞;(iii)某些IgG抗IgE自身抗体可抑制变应原诱导的嗜碱性粒细胞活化。
采用酶联免疫吸附测定法(ELISA)检测和定量血清中的IgE特异性IgG自身抗体。使用嗜碱性粒细胞活化试验,检测血清在有或无变应原存在的情况下激活IgE致敏的人血嗜碱性粒细胞的能力,以及在稳定表达人FcεRI的大鼠嗜碱性细胞系上抑制变应原与特异性IgE结合的能力。
在特应性和非特应性哮喘患者以及对照组中均检测到与游离和FcεRI结合的IgE结合的IgG自身抗体。虽然有些抗体能够激活IgE致敏的嗜碱性粒细胞,但其他抗体则抑制变应原诱导的嗜碱性粒细胞活化,至少部分是通过抑制IgE与特异性变应原的结合来实现的。
天然存在的IgG抗IgE自身抗体可能既诱导又抑制嗜碱性粒细胞活化。它们的作用方式与治疗性IgG抗IgE抗体(如奥马珠单抗)不同。它们可能至少部分解释了产生变应原特异性IgE的特应性个体为何从未出现临床症状,以及奥马珠单抗治疗在重度特应性哮喘中临床疗效为何存在差异。