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Significant IgG subclass heterogeneity in HLA-specific antibodies: Implications for pathogenicity, prognosis, and the rejection response

机译:HLA特异性抗体中明显的IgG亚类异质性:对致病性,预后和排斥反应的影响

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IgG subclasses differ in their ability to fix complement and bind Fc receptors. This study describes a detailed analysis of the distribution of HLA-specific IgG subclasses in order to define how this varies in sensitised waiting-list patients. We found significant variation in the level, presence and combinations of each HLA-specific IgG subclass between and within individuals and this is influenced by the type of sensitising event. Graft failure in particular provokes higher levels of IgG1 (vs transfusion, p = 0.071 and pregnancy, p = 0.042), IgG2 (vs transfusion, p = 0.001 and pregnancy, p = 0.016), and IgG4 (vs transfusion, p = 0.052). Both graft failure and pregnancy tend to stimulate multiple IgG subclass responses against HLA, whereas transfusion stimulated antibodies are dominated by responses limited to IgG1 (p = 0.033) and have a low incidence of IgG4 (p = 0.046). In marked contrast, IgG4 characterised nearly all HLA DQ-specific antibodies stimulated by graft rejection (p = 0.006). Such widely varying IgG subclass heterogeneity is likely to be due to underlying immunological processes dependent on the route of sensitisation. This diversity, which implies functional variation, may help explain why HLA-specific antibodies are an obstacle to transplantation in some circumstances but not others. The subclass association with rejection has potential as a biomarker for chronic rejection. Crown Copyright (C) 2013 American Society for Histocompatibility and Immunogenetics. Published by Elsevier Inc. All rights reserved.
机译:IgG亚类固定补体和结合Fc受体的能力不同。这项研究描述了HLA特异性IgG亚类分布的详细分析,以定义其在敏化候诊患者中的变化。我们发现个体之间和个体内部每个HLA特异性IgG亚类的水平,存在和组合存在显着差异,这受敏化事件类型的影响。移植失败尤其引起更高水平的IgG1(vs输血,p = 0.071和妊娠,p = 0.042),IgG2(vs输血,p = 0.001和妊娠,p = 0.016)和IgG4(vs输血,p = 0.052) 。移植失败和妊娠都倾向于刺激针对HLA的多个IgG亚类反应,而输血刺激的抗体主要受限于IgG1的反应(p = 0.033)且IgG4的发生率低(p = 0.046)。与之形成鲜明对比的是,IgG4几乎表征了移植排斥引起的所有HLA DQ特异性抗体(p = 0.006)。这种广泛变化的IgG亚类异质性很可能是由于依赖于致敏途径的潜在免疫学过程所致。这种多样性意味着功能上的变化,可能有助于解释为什么HLA特异性抗体在某些情况下会成为移植的障碍,而在其他情况下却不会。与排斥反应相关的亚类具有作为慢性排斥反应的生物标志物的潜力。冠版权(C)2013美国组织相容性和免疫遗传学学会。由Elsevier Inc.出版。保留所有权利。

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