摩洛哥南部健康人群中可能与多发性硬化症相关的主要HLA-A、-B、-DR和-DQ基因座的分布

IF 1.7 Q2 MEDICINE, GENERAL & INTERNAL
Abir Fguirouche, Fatimazahra Ouahmani, Ikram Brahim, Raja Hazime, Nissrine Louhab, Najib Kissani, Mohamed Chraa, Brahim Admou
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引用次数: 0

摘要

背景:多种因素导致多发性硬化症(MS)的发生和进展,包括人类白细胞抗原(HLA)分子。其中DRB1*15、DRB1*13、DRB1*03、DRB1*04、DQB1*06、DQB1*02被认为是易感基因,而HLA A2、HLA B44、DRB1*11、DRB1*12被认为是保护性基因。关于摩洛哥人口中这种关联的数据仍然未知。本研究的目的是确定摩洛哥南部健康人群中与多发性硬化(MS)相关的HLA I类(A和B)和II类(DR和DQ)的频率。材料和方法:在2016-2023年期间,对685名摩洛哥健康个体进行了横断面研究,其中包括355名男性和330名女性。在全部检测样本中,685人接受了HLA I类分型,其中305人也受益于HLA II类分型。HLAⅰ类分型采用CDC(补体依赖性细胞毒性)技术(OneLambda™,Los Angeles CA, USA), HLAⅱ类分型采用PCR-SSP(序列特异性引物,OneLambda)或PCR-SSO(序列特异性寡核苷酸),采用Luminex Xmap (Lifecodes, Immucor, Peachtree, Corners, GA, USA)系统。结果:在不同HLA分子中,DRB1*03、DRB1*13、DRB1*15、DRB1*04和DQB1*02分别占19.2%、15.8%、13.31%、12.7%和31%,而具有保护作用的HLA- a2、HLA- b44和HLA-DRB1*11分别占23.31%、9.21%和10.1%。结论:本研究结果表明,在HLAⅱ类易感分子中,DR等位基因组更为普遍,以DRB1*03居多,DQB1*06也有较高的频率,而HLA- a2则标志着所谓的保护特异性。这些结果需要补充研究的支持,特别是在多发性硬化症患者中。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Distribution of Major HLA-A, -B, -DR, and -DQ Loci Potentially Associated with Multiple Sclerosis in a Healthy Population from Southern Morocco.

Background: Many factors contribute to the development and the progression of Multiple Sclerosis (MS), including Human Leukocyte Antigen (HLA) molecules. Some of them are considered as predisposing, like DRB1*15, DRB1*13, DRB1*03, DRB1*04, DQB1*06, DQB1*02, while HLA A2, HLA B44, DRB1*11, and DRB1*12 are rather considered as protective. Data about such associations in the Moroccan population remain unknown. The aim of this study was to determine the frequency of HLA class I (A and B) and II (DR and DQ) linked to Multiple Sclerosis (MS) in a healthy population from the South of Morocco. Materials and Methods: A cross-sectional study was carried out over the 2016-2023 period on 685 Moroccan healthy individuals, including 355 males and 330 females. Of the total sample tested, 685 underwent HLA class I typing, of which 305 also benefited from HLA class II typing. HLA class I typing was executed using the CDC (complement dependent cytotoxicity) technique (OneLambda™, Los Angeles CA, USA), and HLA class II typing was performed by either PCR-SSP (sequence-specific primer, OneLambda) or PCR-SSO (sequence-specific oligonucleotides) using the Luminex Xmap (Lifecodes, Immucor, Peachtree, Corners, GA, USA) system. Results: From different HLA molecules potentially predisposing to MS, our investigations showed that DRB1*03, DRB1*13, DRB1*15, DRB1*04, and DQB1*02 were observed in 19.2%, 15.8%, 13.31%, 12.7% and 31% respectively, while the frequency of those considered as protective, namely HLA-A2, HLA-B44, and HLA-DRB1*11 was 23.31%, 9.21% and 10.1% respectively. Conclusions: The findings of our study give evidence that among predisposing HLA class II molecules, DR allele groups were more prevalent, mostly DRB1*03, with also a high frequency of DQB1*06, while HLA-A2 marked the supposed protective specificities. These results need to be supported by complementary studies particularly in MS patients.

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来源期刊
Clinics and Practice
Clinics and Practice MEDICINE, GENERAL & INTERNAL-
CiteScore
2.60
自引率
4.30%
发文量
91
审稿时长
10 weeks
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