Department of Immunopathology, Post Graduate Institute of Medical Education and Research, Chandigarh 160012 India.
Immunol Invest. 2012;41(2):117-28. doi: 10.3109/08820139.2011.593218. Epub 2011 Aug 1.
The etiology of idiopathic thrombocytopenic purpura (ITP), characterized by destruction of platelets, is still poorly understood. Although genetic as well as immunological factors are thought to play a role in the disease pathogenesis, genetic association studies in terms of major histocompatibility complex (MHC) polymorphisms are scarce and discrepant. Results from previous studies suggest that different populations show varying associations with MHC alleles. Since i) there are inconsistencies in HLA associations, and ii) such an association study does not exist for the Indian subcontinent, we carried out sequence specific priming (SSP)-based genotyping of HLA DRB1 alleles in the North Indian population. Data for such studies is available for two East Asian countries, Japan and China, and the association in both cases is different. Further, among the Japanese population too, there are discrepant results. It was therefore important to analyze such an association in the Indian population, belonging to Southern Asia. Our data shows that none of the alleles have any significant association with ITP. Moreover, in contrast to other studies, comparison made between patients who were responsive to steroid therapy against those who were refractory to steroids, also did not show any association of the HLA DRB1 alleles with steroid responsiveness.
特发性血小板减少性紫癜(ITP)的病因,其特征是血小板破坏,目前仍了解甚少。虽然遗传和免疫因素被认为在疾病发病机制中起作用,但主要组织相容性复合物(MHC)多态性的遗传关联研究很少且存在差异。先前的研究结果表明,不同人群与 MHC 等位基因的关联不同。由于 i)HLA 关联存在不一致,ii)这种关联研究在印度次大陆不存在,因此我们对北印度人群的 HLA DRB1 等位基因进行了基于序列特异性引物(SSP)的基因分型。关于这种研究的资料可用于两个东亚国家,日本和中国,而且这两个国家的关联情况不同。此外,在日本人群中也有不一致的结果。因此,分析属于南亚的印度人群中的这种关联非常重要。我们的数据显示,没有任何等位基因与 ITP 有任何显著关联。此外,与其他研究相反,对激素治疗有反应的患者与对激素治疗无反应的患者进行比较,也没有显示 HLA DRB1 等位基因与激素反应性之间存在任何关联。