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Individualizing Anti-TNF Therapy in Patients With Inflammatory Bowel Disease

2026年6月11日 更新者:Shmuel Kivity, MD

Individualizing Anti-TNF Therapy in Patients With Inflammatory Bowel Disease: Pre-Treatment Prediction of Immunogenicity and Response. A Prospective Observational Study.

This observational study aims to identify genes that may affect how patients with inflammatory bowel disease respond to anti-TNF treatment and why some patients lose response to treatment over time. The study will examine whether genetic markers can help predict which patients are more likely to respond to anti-TNF therapy.

Participants who have not previously received anti-TNF treatment and are about to start advanced therapy will provide a blood sample to test for the genetic markers. Participants will also undergo regular assessments of current treatment, disease activity, and inflammatory markers during follow-up.

調査の概要

詳細な説明

The introduction of anti-TNF therapy was a pivotal milestone in the treatment of inflammatory bowel diseases (IBD). Since then, additional advanced therapies with novel mechanisms of action have been introduced. The plethora of biologics and small molecule drugs increases the ability of IBD patients to achieve therapeutic goals, such as clinical, endoscopic and mucosal healing. However, primary non-response and loss of response remain a challenge and are linked to increase risks related to ongoing inflammation and disease progression.

Predicting the response rates of individual patients to therapy is the goal of a large body of research, linked to clinical characteristics, genetics, microbiome composition and pharmacokinetics. Two promising research topics are Triggering Receptor Expressed in Myeloid cells 1 (TREM1) and HLA-DQA1*05.

TREM1 is a receptor expressed on innate immune cells, known to amplify inflammatory signals triggered by Toll-like receptors, thus contributing to the pathophysiology of acute and chronic inflammatory conditions. Increased protein and mRNA levels of TREM1 in whole blood and colonic biopsies are associated with clinical and endoscopic non-response to anti-TNF. The suggested best cut-off point is 3.346 folds increase in mRNA expression in whole blood samples, with a specificity of 91.3% and sensitivity of 58.1%.

HLA class II gene HLA-DQA1 is expressed by antigen presenting cells and encodes the α-chain of the HLA-DQ heterodimer that forms part of the antigen-binding site where epitopes are presented to T-helper cells. Carriage of HLA-DQA1*05 allele confers a 2-fold risk of immunogenicity to anti-TNF therapy. This risk was mitigated using a concomitant immunomodulator.

Our goal is to evaluate the predictive power of these tests separately in a prospective observational study, and assess whether combining the tests' outcomes prior to initiation of anti-TNF therapy improve therapy outcomes, including efficacy and durability.

The aims of this study are to assess the effectiveness of each test, and the combined tests for TREM1 and HLA-DQA1*05 to improve clinical and endoscopic response and remission rates, in patients with IBD starting anti-TNF therapy. The study will also assess the effectiveness of each test, and the combined tests for TREM1 and HLA-DQA1*05 in improving anti-TNF treatment durability and immunogenicity.

Participants will provide blood samples prior to treatment initiation for the assessment of HLA-DQA1*05 using quantitative real-time polymerase chain reaction (qRT-PCR) and TREM1 levels using an enzyme-linked immunosorbent assay (ELISA).

Drug and antibody levels will be measured at weeks 8, 24, and 52. Participants will also undergo periodic evaluations of their medical therapy and clinical disease activity throughout the study period.

Endoscopic disease activity (endoscopic MAYO score [eMAYO] for UC, and simple endoscopic score [SES-CD] for CD) will be evaluated with endoscopy 6-12 months after starting therapy, if performed as standard of care by the treating physician's discretion.

Statistical analysis Continuous variables will be presented as mean ± standard deviation for normal distribution and median with interquartile range for non-normal distribution. Nominal variables will be presented as proportions. Pearson correlation coefficient will be calculated to find association between HLA-DQA1*05 and anti-TNF immunogenicity, and between TREM1 expression and anti-TNF response rates. ROC curve with Youden index will be used to calculated area under the curve and optimal tests results predicting immunogenicity and response to therapy. Chi-Square test will be used to test the association between nominal variables. Comparison of continued variables groups will be performed by the independent samples t-test for variables which distribute normally, and by the Mann-Whitney test for variables which did not distribute normally. Normality will be tested graphically and using the Shapiro Wilk's test. Comparison of immunogenicity and response to therapy between study visits, and evaluation of the overtime trends in these parameters, in accordance with HLA-DQA1*05 and TREM1 tests results, will be performed by using the linear mixed model analysis (three or more visits) and by the paired sample T test (two visits). Statistical significance was set at P ≤ 0.05. All statistical analyses will be performed using R-4.3.2 for Windows.

研究の種類

観察的

入学 (推定)

40

連絡先と場所

このセクションには、調査を実施する担当者の連絡先の詳細と、この調査が実施されている場所に関する情報が記載されています。

研究連絡先

研究連絡先のバックアップ

研究場所

      • Tel Aviv、イスラエル
        • 募集
        • Dep. of Gastroenterology, Tel Aviv Sourasky Medical Center
        • コンタクト:

参加基準

研究者は、適格基準と呼ばれる特定の説明に適合する人を探します。これらの基準のいくつかの例は、人の一般的な健康状態または以前の治療です。

適格基準

就学可能な年齢

  • 大人
  • 高齢者

健康ボランティアの受け入れ

いいえ

サンプリング方法

非確率サンプル

調査対象母集団

Patients followed in the IBD unit in TLVMC starting or switching biologic therapy

説明

Inclusion Criteria:

  • Established IBD: Crohn's disease (CD) or ulcerative colitis (UC)
  • Anti-TNF naïve
  • Clinically active disease (HBI>5 for CD, p-MS≥ 3 for UC)
  • Elevated inflammatory indices CRP>10 or fecal calprotectin>250

Exclusion Criteria:

  • Unable to provide informed consent
  • Anti-TNF experienced
  • Unable to complete the study protocol

研究計画

このセクションでは、研究がどのように設計され、研究が何を測定しているかなど、研究計画の詳細を提供します。

研究はどのように設計されていますか?

デザインの詳細

コホートと介入

グループ/コホート
介入・治療
IBD patients
naïve to anti-TNF therapy
Patients will receive therapy as part of their standard care according to the standard dose
他の名前:
  • アダリムマブ(ヒュミラ)
  • Infliximab (Remicade)
  • Certolizumab pegol (Cimzia)
  • Golimumab (Simponi)

この研究は何を測定していますか?

主要な結果の測定

結果測定
メジャーの説明
時間枠
Rates of clinical response in UC patients
時間枠:Week 8
Defined as decrease from baseline in partial Mayo score (p-MS) of ≥30%, plus a decrease in each sub score of ≥1.
Week 8
Rates of clinical response in UC patients
時間枠:Week 24
Defined as decrease from baseline in partial Mayo score (p-MS) of ≥30%, plus a decrease in each sub score of ≥1.
Week 24
Rates of clinical response in UC patients
時間枠:Week 52
Defined as decrease from baseline in partial Mayo score (p-MS) of ≥30%, plus a decrease in each sub score of ≥1.
Week 52
Rates of clinical response in CD patients
時間枠:Week 8
Defined as decrease of at least 30% in Harvey-Bradshaw index (HBI).
Week 8
Rates of clinical response in CD patients
時間枠:Week 24
Defined as decrease of at least 30% in Harvey-Bradshaw index (HBI).
Week 24
Rates of clinical response in CD patients
時間枠:Week 52
Defined as decrease of at least 30% in Harvey-Bradshaw index (HBI).
Week 52
Rates of clinical remission for UC
時間枠:Week 8
p-MS <3 and no sub score>1
Week 8
Rates of clinical remission for UC
時間枠:Week 24
p-MS <3 and no sub score>1
Week 24
Rates of clinical remission for UC
時間枠:Week 52
p-MS <3 and no sub score>1
Week 52
Rates of clinical remission for CD
時間枠:Week 8
defined as HBI≤4
Week 8
Rates of clinical remission for CD
時間枠:Week 24
defined as HBI≤4
Week 24
Rates of clinical remission for CD
時間枠:Week 52
defined as HBI≤4
Week 52

二次結果の測定

結果測定
メジャーの説明
時間枠
c-reactive protein (CRP) levels
時間枠:Week 8
Change from baseline in CRP levels
Week 8
CRP levels
時間枠:Week 24
Change from baseline in CRP levels
Week 24
CRP levels
時間枠:Week 52
Change from baseline in CRP levels
Week 52
Fecal calprotectin levels
時間枠:Week 8
Change from baseline in fecal calprotectin levels
Week 8
Fecal calprotectin levels
時間枠:Week 24
Change from baseline in fecal calprotectin levels
Week 24
Fecal calprotectin levels
時間枠:Week 52
Change from baseline in fecal calprotectin levels
Week 52
Rates of endoscopic response for UC
時間枠:Up to 12 months after initiating treatment
Endoscopic response defined as Mayo endoscopic sub-score (MES) ≤1
Up to 12 months after initiating treatment
Rates of endoscopic response for CD
時間枠:Up to 12 month after initiation of treatment
Endoscopic response defined as decrease in CDEIS>50%
Up to 12 month after initiation of treatment
Rates of endoscopic remission for UC
時間枠:Up to 12 month after initiation of treatment
defined as MES=0
Up to 12 month after initiation of treatment
Rates of endoscopic remission for CD
時間枠:Up to 12 month after initiation of treatment
defined as CDEIS<6 (CDEIS≤4 for isolated ileitis).
Up to 12 month after initiation of treatment
Immunogenicity
時間枠:Week 8
anti-drug antibodies levels
Week 8
Immunogenicity
時間枠:Week 24
anti-drug antibodies levels
Week 24
Immunogenicity
時間枠:Week 52
anti-drug antibodies levels
Week 52
Drug levels
時間枠:Week 8
Serum drug levels
Week 8
Drug levels
時間枠:Week 24
Serum drug levels
Week 24
Drug levels
時間枠:Week 52
Serum drug levels
Week 52
Therapeutic success
時間枠:Through study completion, an average of 1 year
Therapy persistence or discontinuation
Through study completion, an average of 1 year

協力者と研究者

ここでは、この調査に関係する人々や組織を見つけることができます。

スポンサー

捜査官

  • 主任研究者:Ayal Hirsch, MD、Tel Aviv Sourasky University Medical Center

研究記録日

これらの日付は、ClinicalTrials.gov への研究記録と要約結果の提出の進捗状況を追跡します。研究記録と報告された結果は、国立医学図書館 (NLM) によって審査され、公開 Web サイトに掲載される前に、特定の品質管理基準を満たしていることが確認されます。

主要日程の研究

研究開始 (実際)

2025年1月4日

一次修了 (推定)

2028年5月1日

研究の完了 (推定)

2028年12月1日

試験登録日

最初に提出

2026年5月31日

QC基準を満たした最初の提出物

2026年6月11日

最初の投稿 (実際)

2026年6月12日

学習記録の更新

投稿された最後の更新 (実際)

2026年6月12日

QC基準を満たした最後の更新が送信されました

2026年6月11日

最終確認日

2026年5月1日

詳しくは

本研究に関する用語

個々の参加者データ (IPD) の計画

個々の参加者データ (IPD) を共有する予定はありますか?

未定

IPD プランの説明

At this time, there are no plans for data sharing or external collaborations. If data sharing is pursued in the future; only de-identified participant data will be shared, including demographic information, clinical indices and response to treatment.

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米国FDA規制医薬品の研究

いいえ

米国FDA規制機器製品の研究

いいえ

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