利用人白细胞抗原基因预测炎症性肠病患者对生物治疗的耐药性。

IF 3.9 3区 医学 Q1 GASTROENTEROLOGY & HEPATOLOGY
Therapeutic Advances in Gastroenterology Pub Date : 2025-07-11 eCollection Date: 2025-01-01 DOI:10.1177/17562848251353293
Ângela Domingues, Ana Carvalho, António Martinho, Caroline Soares, Diana Martins, Paula Sousa, Ricardo Araújo, Eugénia Cancela, Américo Silva, Paula Ministro
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引用次数: 0

摘要

背景:抗肿瘤坏死因子(TNF)治疗炎症性肠病(IBD)的疗效经常受到抗药抗体的影响。在这种情况下,人类白细胞抗原(HLA)-DQA1*05等位基因与抗肿瘤坏死因子的抗药抗体的形成、反应丧失和治疗停止显著相关。目的:我们旨在确定HLA-DQA1*05基因分型是否与IBD患者有临床意义的结局相关。设计:对IBD患者进行了一项单中心前瞻性研究,这些患者接受naïve生物治疗,并开始使用抗tnf药物、vedolizumab或ustekinumab进行治疗。方法:对所有患者进行HLA-DQA1*05基因分型。主要终点是在第54周达到包括临床、生化和内窥镜缓解在内的综合结果,并按HLA-DQA1*05状态分层。次要终点包括治疗持续性的评估和抗药物抗体的发展。结果:100例biologic-naïve IBD患者启动生物治疗纳入研究(抗tnf 72例,vedolizumab 18例,ustekinumab 10例);其中43%为HLA-DQA1*05阳性。HLA-DQA1*05等位基因的存在与较差的临床结果(定义为第54周临床、生化和内镜缓解的复合)无关,在接受抗tnf药物、vedolizumab或ustekinumab治疗的患者中。此外,HLA-DQA1*05基因型与治疗持久性降低或免疫原性增加之间无显著相关性。结论:在我们的IBD患者队列中,HLA-DQA1*05基因型与更高的治疗停止风险或更差的临床结果无关。试验注册:我们能依靠HLA预测IBD患者对生物治疗的耐药性吗?URL: https://clinicaltrials.gov/study/NCT05040854?cond=Can%20we%20rely%20on%20HLA&rank=1。注册号:NCT05040854 (clinicaltrials.gov)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Predicting resistance to biological therapy using human leukocyte antigen genes in patients with inflammatory bowel disease.

Background: The efficacy of anti-tumor necrosis factor (TNF) therapy in inflammatory bowel disease (IBD) is often compromised by the development of antidrug antibodies. In this setting, the human leukocyte antigen (HLA)-DQA1*05 allele has been significantly associated with the formation of antidrug antibodies to anti-TNF agents, loss of response, and treatment discontinuation.

Objectives: We aimed to determine whether HLA-DQA1*05 genotyping is associated with clinically meaningful outcomes in patients with IBD.

Design: A single-center, prospective study was conducted on patients with IBD who were naïve to biological treatment and were initiating therapy with anti-TNF agents, vedolizumab, or ustekinumab.

Methods: All patients were genotyped for HLA-DQA1*05. The primary endpoint was the achievement of a composite outcome encompassing clinical, biochemical, and endoscopic remission at week 54, stratified by HLA-DQA1*05 status. The secondary endpoints included the evaluation of therapeutic persistence and the development of antidrug antibodies.

Results: One hundred biologic-naïve patients with IBD initiating biological therapy were included in the study (72 on anti-TNF, 18 on vedolizumab, and 10 on ustekinumab); of these, 43% were HLA-DQA1*05 positive. The presence of the HLA-DQA1*05 allele was not associated with worse clinical outcomes, defined as the composite of clinical, biochemical, and endoscopic remission at week 54, in patients treated with anti-TNF agents, vedolizumab, or ustekinumab. In addition, no significant correlation was observed between the HLA-DQA1*05 genotype and reduced therapy persistence or increased immunogenicity.

Conclusion: In our cohort of patients with IBD, the HLA-DQA1*05 genotype was not associated with a higher risk of treatment cessation or worse clinical outcomes.

Trial registration: Can we rely on HLA to predict resistance to biological therapy in patients with IBD?URL: https://clinicaltrials.gov/study/NCT05040854?cond=Can%20we%20rely%20on%20HLA&rank=1. Registration number: NCT05040854 (clinicaltrials.gov).

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来源期刊
Therapeutic Advances in Gastroenterology
Therapeutic Advances in Gastroenterology GASTROENTEROLOGY & HEPATOLOGY-
CiteScore
6.70
自引率
2.40%
发文量
103
审稿时长
15 weeks
期刊介绍: Therapeutic Advances in Gastroenterology is an open access journal which delivers the highest quality peer-reviewed original research articles, reviews, and scholarly comment on pioneering efforts and innovative studies in the medical treatment of gastrointestinal and hepatic disorders. The journal has a strong clinical and pharmacological focus and is aimed at an international audience of clinicians and researchers in gastroenterology and related disciplines, providing an online forum for rapid dissemination of recent research and perspectives in this area. The editors welcome original research articles across all areas of gastroenterology and hepatology. The journal publishes original research articles and review articles primarily. Original research manuscripts may include laboratory, animal or human/clinical studies – all phases. Letters to the Editor and Case Reports will also be considered.
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