Kapustin Sergey I, Popova Tamara I, Lyschov Anton A, Togo Alexander V, Abdulkadyrov Kudrat M, Blinov Michail N
Institute of Haematology and Transfusiology, Laboratory of Biochemistry, St.-Petersburg, Russia.
Pathol Oncol Res. 1997;3(2):106-108. doi: 10.1007/BF02907803.
The association between severe aplastic anemia (AA) and DR2 antigen seems to be well established. However, since discrimination between two DR2-associated splits, namely DR15 and DR16, rarely was performed, it remains unclear whether one or both of these subvariants are responsible for AA susceptibility. In this study, we have analyzed the HLA-DR allelic distribution in a group of 37 AA patients of slavic origin from North-Western Russia. The experimental design included PCR-based amplification of DRB-specific sequences, followed by reverse dot-blot hybridization of the biotinylated PCR-product with the set of sequence-specific oligonucleotide probes. HLA-DRB alleles were identified by non-radioactive enzymatic reaction, then standard serological specificities of HLA-DR antigen were estimated according to the WHO nomenclature. Whereas DR15 subtype occurred more often in the patients (23.0% vs. 13.3%, p< 0.05), DR16 split did not show the same tendency. The results, show the overall predominance of HLA-DR2 specificity (DR15+DR16) did not reach statistical significance (24.4% vs.17.5%, p<0.2). Thus, we conclude that repeatedly reported DR2 frequency increase in AA patients is mainly attributed to the prevalence of DR15 subtype.
重度再生障碍性贫血(AA)与DR2抗原之间的关联似乎已得到充分证实。然而,由于很少对两种与DR2相关的亚型,即DR15和DR16进行区分,目前尚不清楚这些亚变体中的一种还是两种都与AA易感性有关。在本研究中,我们分析了一组来自俄罗斯西北部的37名斯拉夫裔AA患者的HLA-DR等位基因分布。实验设计包括基于PCR的DRB特异性序列扩增,随后将生物素化的PCR产物与一组序列特异性寡核苷酸探针进行反向点杂交。通过非放射性酶促反应鉴定HLA-DRB等位基因,然后根据世界卫生组织的命名法估计HLA-DR抗原的标准血清学特异性。虽然DR15亚型在患者中出现的频率更高(23.0%对13.3%,p<0.05),但DR16亚型并未表现出相同的趋势。结果显示,HLA-DR2特异性(DR15+DR16)的总体优势未达到统计学意义(24.4%对17.5%,p<0.2)。因此,我们得出结论,AA患者中反复报道的DR2频率增加主要归因于DR15亚型的流行。