人类白细胞抗原等位基因和母体微嵌合在日本儿童早发性溃疡性结肠炎中的作用。

IF 4.3 3区 医学 Q1 GASTROENTEROLOGY & HEPATOLOGY
Masanori Toda, Keisuke Jimbo, Mitsuyoshi Suzuki, Masumi Nagata, Nobuyasu Arai, Kaori Tokushima, Eri Miyata, Yuka Nagano, Yuki Koike, Keiichi Uchida, Takahiro Kudo, Yuji Toiyama, Toshiaki Shimizu
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引用次数: 0

摘要

背景:极早发性溃疡性结肠炎(VEO-UC)是一种严重的炎症性肠病,表现在6岁之前。与典型的儿童UC相比,它具有独特的遗传和免疫因素。本研究旨在探讨特异性人白细胞抗原(HLA)等位基因和母体微嵌合(MMc)在日本人群VEO-UC发病中的作用。方法:本研究纳入27例VEO-UC患者,其中4例行结直肠切除术。采用聚合酶链反应-序列特异性寡核苷酸探针(PCR-SSOP)进行HLA分型,并与日本普通人群进行比较。采用免疫组织化学和荧光原位杂交技术评价肠组织中MMc的表达。HLA与日本普通人群的数据进行了统计比较,使用Bonferroni校正来处理多重比较。结果:HLA-B52和HLA-DR15在VEO-UC病例中比在日本普通人群中更普遍,尽管在Bonferroni校正后统计学意义降低。3例VEO-UC患者在肠道组织中发现了MMc,而对照组未发现MMc。在一些病例中,母体HLA与VEO-UC相关的特定等位基因一致,表明母体免疫参与了该疾病的发病机制。结论:VEO-UC似乎与成人UC具有相同的遗传特征,例如与HLA-B52和HLA-DR15相关,并且也受到母体免疫贡献的影响,如受影响组织中存在MMc。这些发现强调了VEO-UC发病机制中遗传和免疫因素之间复杂的相互作用,并强调了进一步研究开发针对这些机制的靶向治疗策略的必要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The Role of Human Leukocyte Antigen Alleles and Maternal Microchimerism in Very-Early-Onset Ulcerative Colitis in Japanese Children.

Background: Very-early-onset ulcerative colitis (VEO-UC) is a severe form of inflammatory bowel disease that manifests before the age of 6 years. Compared to typical pediatric UC, it is characterized by distinct genetic and immunological factors. This study aimed to investigate the roles of specific human leukocyte antigen (HLA) alleles and maternal microchimerism (MMc) in the pathogenesis of VEO-UC in a Japanese population.

Methods: This study included 27 VEO-UC patients, including 4 patients treated with colorectal resection. HLA typing was performed by polymerase chain reaction-sequence-specific oligonucleotide probing (PCR-SSOP) and compared with the Japanese general population. Immunohistochemistry and fluorescence in situ hybridization were used to evaluate MMc in intestinal tissues. Statistical comparisons of HLA were performed against data from the general Japanese population, with Bonferroni corrections applied to handle multiple comparisons.

Results: HLA-B52 and HLA-DR15 were more prevalent in cases of VEO-UC than in the general Japanese population, although the statistical significance decreased after the Bonferroni correction. MMc was found in the intestinal tissues of three VEO-UC cases, whereas it was absent in the control UC cases. Maternal HLA concordance with specific alleles associated with VEO-UC was noted in several cases, suggesting maternal immune involvement in the pathogenesis of the disease.

Conclusions: VEO-UC seems to share genetic traits with adult UC, such as an association with HLA-B52 and HLA-DR15, and is also affected by maternal immune contributions, as shown by the presence of MMc in the affected tissues. These findings highlight the complex interaction between genetic and immunological factors in the pathogenesis of VEO-UC and underscore the need for further research to develop targeted therapeutic strategies that address these mechanisms.

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来源期刊
Inflammatory Bowel Diseases
Inflammatory Bowel Diseases 医学-胃肠肝病学
CiteScore
9.70
自引率
6.10%
发文量
462
审稿时长
1 months
期刊介绍: Inflammatory Bowel Diseases® supports the mission of the Crohn''s & Colitis Foundation by bringing the most impactful and cutting edge clinical topics and research findings related to inflammatory bowel diseases to clinicians and researchers working in IBD and related fields. The Journal is committed to publishing on innovative topics that influence the future of clinical care, treatment, and research.
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