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妊娠诱导的儿童特异性致敏的频率和决定因素。

Frequency and determinants of pregnancy-induced child-specific sensitization.

机构信息

Immunobiology, University Hospital Basel, Switzerland.

出版信息

Am J Transplant. 2013 Mar;13(3):746-53. doi: 10.1111/ajt.12048. Epub 2013 Jan 11.

Abstract

The aim of this study was to define the frequency and determinants of pregnancy-induced child-specific sensitization shortly after full-term delivery using sensitive single HLA-antigen beads (SAB) and high resolution HLA-typing of the mothers and their children (n = 301). A positive SAB result was defined by a background normalized ratio >1 or a mean fluorescence intensity (MFI) >300, >500 and >1000, respectively. The overall frequency of pregnancy-induced sensitization determined by SAB shortly after full-term delivery was between 45% (MFI > 1000 cut-off) and 76% (ratio cut-off). The rate of child-specific sensitization at the HLA-A/B/C/DRB1 loci was between 28% (MFI > 1000 cut-off) and 38% (ratio cut-off). The number of live birth was associated with a higher frequency of sensitization, which was driven by child-specific, but not third party HLA-antibodies. There was a clear hierarchy of sensitization among the investigated loci (B-locus: 31%; A-locus: 26%; DRB1-locus: 20%; C-locus: 15%; p < 0.0001). Some mismatched paternal HLA-antigens led to a significantly higher rate of sensitization than the average (e.g. HLA-A2, HLA-B49, HLA-B51, HLA-C*15). Furthermore, the mother's own HLA-phenotype--especially HLA-A/B homozygosity--was associated with a higher rate and broadness of sensitization. The number of mismatched HLA-A/B/C eplets strongly correlated with the rate of child-specific class I sensitization.

摘要

本研究旨在使用敏感的单 HLA 抗原珠 (SAB) 和母亲及其儿童的高分辨率 HLA 分型,在足月分娩后不久定义妊娠诱导的针对儿童的特异性致敏的频率和决定因素 (n = 301)。通过 SAB 在足月分娩后不久确定的妊娠诱导致敏的阳性结果定义为背景归一化比值>1 或平均荧光强度 (MFI)>300、>500 和 >1000。通过 SAB 确定的妊娠诱导的致敏的总体频率在 45%(MFI>1000 截止值)和 76%(比值截止值)之间。HLA-A/B/C/DRB1 基因座上的儿童特异性致敏率在 28%(MFI>1000 截止值)和 38%(比值截止值)之间。活产数与致敏频率增加相关,致敏是由儿童特异性但不是第三方 HLA 抗体驱动的。在所研究的基因座中,致敏存在明显的等级结构(B 基因座:31%;A 基因座:26%;DRB1 基因座:20%;C 基因座:15%;p<0.0001)。一些不匹配的父系 HLA 抗原导致致敏率明显高于平均值(例如 HLA-A2、HLA-B49、HLA-B51、HLA-C*15)。此外,母亲自身的 HLA 表型-特别是 HLA-A/B 纯合性-与更高的致敏率和更广泛的致敏有关。不匹配的 HLA-A/B/C 表位的数量与儿童特异性 I 类致敏的速率强烈相关。

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