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埃及风湿性瓣膜病患儿的HLA I类和II类HLA DRB谱

HLA class I and class II HLA DRB profiles in Egyptian children with rheumatic valvular disease.

作者信息

El-Hagrassy Nashwa, El-Chennawi Farha, Zaki Maysaa El-Sayed, Fawzy Hossam, Zaki Adel, Joseph Nabeil

机构信息

October 6 University, October 6 City, Egypt.

出版信息

Pediatr Cardiol. 2010 Jul;31(5):650-6. doi: 10.1007/s00246-010-9663-3. Epub 2010 Feb 10.

DOI:10.1007/s00246-010-9663-3
PMID:20145915
Abstract

Poststreptococcal sequelae, especially acute rheumatic fever/rheumatic heart disease continues to occur in significant proportions in many parts of the world, especially in less developed countries. An important factor in the study of rheumatic heart disease is the human genetic susceptibility to the disease. The aim of the present study was to detect the most prevalent HLA class I and class II types associated with risk of rheumatic heart disease in Egyptian children. Our study was performed on 100 patients with rheumatic valvular heart diseases and 71 control subjects. Patients were recruited from the Heart Institute, Embaba, Egypt. HLA typing for HLA class I was performed by serotyping and HLDR allele genotyping was performed using INNO-LiPA kits. In the study of HLA class I, there was a statistically significant increase in the B5 allele (P = 0.03; odds ratio, 3.46 [1.12-10.72]) in patients compared to controls, while B49 and B52 alleles (P = 0.004 and P = 0.02) were found in controls only. There was a statistically significant increase in HLA DR* 04-02, 3.46 (1.12-10.72) and HLA DR 10-0101 5.75 (1.27-25.98) in patients. Meanwhile HLA DR1309120 was found only in controls (P = 0.02). Our study provides further information on the genetic predisposition for rheumatic valvular disease and the protective genotypes in rheumatic heart disease. Further insight into the molecular mechanisms of the disease will be a useful tool for predicting clinical outcome in those patients and, thus, potentially offer new means and approaches to treatment and prophylaxis, including a potential vaccine.

摘要

链球菌感染后后遗症,尤其是急性风湿热/风湿性心脏病,在世界许多地区,特别是在欠发达国家,仍有相当比例的病例发生。风湿性心脏病研究中的一个重要因素是人类对该病的遗传易感性。本研究的目的是检测埃及儿童中与风湿性心脏病风险相关的最常见的 HLA Ⅰ类和Ⅱ类类型。我们的研究对 100 例风湿性瓣膜性心脏病患者和 71 例对照受试者进行。患者来自埃及恩巴卜心脏研究所。HLA Ⅰ类的 HLA 分型通过血清学分型进行,HLDR 等位基因基因分型使用 INNO-LiPA 试剂盒进行。在 HLA Ⅰ类研究中,与对照组相比,患者中 B5 等位基因有统计学意义的增加(P = 0.03;优势比,3.46 [1.12 - 10.72]),而 B49 和 B52 等位基因(P = 0.004 和 P = 0.02)仅在对照组中发现。患者中 HLA DR*04 - 02 有统计学意义的增加,为 3.46(1.12 - 10.72),HLA DR 10 - 0101 为 5.75(1.27 - 25.98)。同时,HLA DR1309120 仅在对照组中发现(P = 0.02)。我们的数据为风湿性瓣膜病的遗传易感性和风湿性心脏病的保护性基因型提供了进一步的信息。对该疾病分子机制的进一步深入了解将成为预测这些患者临床结局的有用工具,从而可能为治疗和预防提供新的手段和方法,包括潜在的疫苗。

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