用于治疗炎性肠病的生物制剂的免疫原性。

Q3 Medicine
Mariam Bqain, Alex Efimov, David Baker, Angray S Kang
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引用次数: 1

摘要

回顾的目的:在这里,我们批判性地评价炎症性肠病患者免疫治疗失败的文献。特别是抗药物抗体的产生,以及随后的反应丧失是IBD患者免疫治疗失败的主要原因。从“标准”经验剂量递增方法转向抗tnf - α治疗药物监测的好处进行了探讨。最近的发现:美国胃肠病学协会和英国胃肠病学协会目前都推荐使用反应性治疗药物监测来指导治疗炎症性肠病患者的活动性疾病。然而,需要进一步的研究来证明主动治疗药物监测方法在缓解的IBD患者中的有效性。摘要:抗药物抗体的个性化监测方法和治疗性药物监测相结合,可以在临床症状出现之前预测药物失效,并允许及时切换到替代药物,从而为炎症性肠病患者提供有益的治疗结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Immunogenicity of biologics used in the treatment of inflammatory bowel disease.

Purpose of the review: Here we critically evaluate the literature on immunotherapy failure in inflammatory bowel disease patients. In particular anti-drug antibody production, and subsequently loss of response as the primary cause of immunotherapy failure in IBD patients. The benefits of shifting from the "standard" empirical dose escalation approach to therapeutic drug monitoring with anti-TNFα therapy is explored.

Recent findings: The American Gastroenterology Association and British Society of Gastroenterology both currently recommend the use of reactive therapeutic drug monitoring to guide treatment, following loss of response in inflammatory bowel disease patients with active disease. However, further research is required to prove the efficacy of a proactive therapeutic drug monitoring approach alone in remitted IBD patients.

Summary: A combination of personalised monitoring approach for anti-drug antibodies and therapeutic drug monitoring could provide beneficial treatment outcome for people with inflammatory bowel disease by predicting drug failure prior to clinical symptoms and allowing timely switching to an alternative drug.

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来源期刊
Human Antibodies
Human Antibodies Medicine-Immunology and Allergy
CiteScore
3.50
自引率
0.00%
发文量
27
期刊介绍: Human Antibodies is an international journal designed to bring together all aspects of human hybridomas and antibody technology under a single, cohesive theme. This includes fundamental research, applied science and clinical applications. Emphasis in the published articles is on antisera, monoclonal antibodies, fusion partners, EBV transformation, transfections, in vitro immunization, defined antigens, tissue reactivity, scale-up production, chimeric antibodies, autoimmunity, natural antibodies/immune response, anti-idiotypes, and hybridomas secreting interesting growth factors. Immunoregulatory molecules, including T cell hybridomas, will also be featured.
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