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人类白细胞抗原对乙肝疫苗抗体反应的作用。

Contribution of human leukocyte antigens to the antibody response to hepatitis B vaccination.

作者信息

McDermott A B, Zuckerman J N, Sabin C A, Marsh S G, Madrigal J A

机构信息

Anthony Nolan Research Institute, Royal Free Hospital, London, United Kingdom.

出版信息

Tissue Antigens. 1997 Jul;50(1):8-14. doi: 10.1111/j.1399-0039.1997.tb02827.x.

DOI:10.1111/j.1399-0039.1997.tb02827.x
PMID:9243749
Abstract

We present here the analysis of 86 individuals who were true antibody nonresponders to a vaccine containing hepatitis B surface antigen. The HLA type of these individuals and of 248 controls were determined by serology for HLA class I and by molecular typing for the HLA class II loci DRB1 and DQB1. Subsequent analysis of the results revealed that HLA-DRB10701 and HLA-DQB102 were significantly associated with antibody non-response to the "S"-containing vaccine compared with the HLA control population. Further, we found that the antibody non-response was also significantly associated with the above antigens when found in linkage disequilibrium on the HLA haplotype DRB10701; DQB10202. The hepatitis B surface antigen vaccine antibody nonresponder group, comprising 86 individuals, were revaccinated with a novel vaccine Hep B-3, containing both preS1- and preS2-derived proteins in addition to hepatitis B surface antigen, to circumvent their previous nonresponsiveness. The hepatitis B surface antigen antibody results from this group of patients show that 30 of the 86 individuals remained antibody non-responders and that 24 individuals (80%) expressed the HLA-DQB102 and that 21 individuals (70%) expressed HLA-DRB10701. Our results indicate that antibody nonresponse to the Hep B-3 vaccine is significantly associated with an extended HLA haplotype B44; DRB10701; DQB10202. A possible indication of these results is that antibody nonresponse to Hep B-3 vaccine is linked with the HLA allele DQB1*0202. These findings may have an important impact on future vaccine design.

摘要

我们在此展示了对86名对含乙型肝炎表面抗原疫苗真正无抗体应答者的分析。通过血清学检测I类HLA,以及通过分子分型检测II类HLA基因座DRB1和DQB1,确定了这些个体以及248名对照者的HLA类型。对结果的后续分析显示,与HLA对照人群相比,HLA - DRB10701和HLA - DQB102与对含“S”疫苗的无抗体应答显著相关。此外,我们发现当上述抗原在HLA单倍型DRB10701; DQB10202上处于连锁不平衡状态时,无抗体应答也与之显著相关。由86名个体组成的乙型肝炎表面抗原疫苗无抗体应答组,再次接种了一种新型疫苗Hep B - 3,该疫苗除了含有乙型肝炎表面抗原外,还含有前S1和前S2衍生蛋白,以克服他们之前的无应答情况。这组患者的乙型肝炎表面抗原抗体结果显示,86名个体中有30名仍然无抗体应答,24名个体(80%)表达HLA - DQB102,21名个体(70%)表达HLA - DRB10701。我们的结果表明,对Hep B - 3疫苗的无抗体应答与扩展的HLA单倍型B44; DRB10701; DQB10202显著相关。这些结果的一个可能暗示是,对Hep B - 3疫苗的无抗体应答与HLA等位基因DQB1*0202有关。这些发现可能对未来的疫苗设计产生重要影响。

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