Evidence map›Paper›PMID 42766208›Full record

ReviewIndian journal of gastroenterology : official journal of the Indian Society of Gastroenterology2026

Tumor necrosis factor-like cytokine 1 A antagonists for inflammatory bowel disease: A systematic review and meta-analysis.

Mukesh Sharma Paudel, Vishal Sharma, Kumud Bhattarai, Chhagan Lal Birda, Khushboo Goel, Ajay Yadav, Shivaom Chaurasia, Milan Shrestha, Mukesh Kumar Ranjan

Abstract readReview
PubMed Publisher
In one paragraph

Review in Indian journal of gastroenterology : official journal of the Indian Society of Gastroenterology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Mukesh Sharma PaudelDepartment of Gastroenterology, Bir Hospital, Kathmandu, Bagmati, Nepal. drmuku@gmail.com.
Vishal SharmaDepartment of Gastroenterology, Post Graduate Institute of Medical Education and Research, Chandigarh, 160 012, India.
Kumud BhattaraiDepartment of Gastroenterology, Bir Hospital, Kathmandu, Bagmati, Nepal.
Chhagan Lal BirdaDepartment of Gastroenterology, All India Institute of Medical Sciences, Jodhpur, 342 005, India.
Khushboo GoelDepartment of Periodontology, Institute of Medicine, Kathmandu, Bagmati, Nepal.
Ajay YadavDepartment of Gastroenterology, Bir Hospital, Kathmandu, Bagmati, Nepal.
Shivaom ChaurasiaDepartment of Gastroenterology, Nepal Mediciti Hospital, Kathmandu, Bagmati, Nepal.
Milan ShresthaDepartment of Gastroenterology, Bir Hospital, Kathmandu, Bagmati, Nepal.
Mukesh Kumar RanjanDepartment of Gastroenterology, Bir Hospital, Kathmandu, Bagmati, Nepal.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

objectivesThe therapeutic paradigm in inflammatory bowel disease (IBD) is rapidly evolving. Tumor necrosis factor-like cytokine 1A (TL1A) antagonists are agents with potential to mitigate both inflammation and fibrosis. Available studies show early signals of efficacy of this novel therapeutic class. We summarize the available literature on the use anti-TL1A, through this systematic review and meta-analysis.

methodsWe conducted a systematic review and meta-analysis to assess the outcome of TL1A antagonists in patients with ulcerative colitis and Crohn's disease. We searched PubMed, EMBASE, Scopus and CENTRAL electronic databases for eligible studies through October 10, 2025. All studies with TL1A antagonists reporting outcome in adult IBD patients were included. We assessed clinical response, clinical remission, endoscopic improvement and remission and Histologic Endoscopic Mucosal Improvement (HEMI). We also assessed the adverse events (AEs) with anti-TL1A use.

resultsOf the 431 studies screened, 12 were included in the final analysis. The pooled clinical response rate was seen in 67% of patients with ulcerative colitis and 58% of patients with Crohn's disease, with an odds ratio (OR) of 4.07 (95% CI 1.55-10.70) and 2.96 (95% CI 1.36-6.42), respectively. Anti-TL1A appeared to achieve clinical remission with OR 3.75 (95% CI 2.04-6.89). The pooled proportion of UC patients with endoscopic improvement and remission were 41% (95% CI 0.36-0.46) and 13% (95% CI 0.10-0.17), respectively. Patients with UC on anti-TL1A had an odds of achieving HEMI of 5.51 (95% CI 1.86-16.34). The most common reported adverse events (AEs) were mild and included infections and infestations. AEs occurred in 48.3% patients with UC and 49.2% of patients with CD with serious AEs reported in 3.9% patients with UC and 4.6% patients with CD.

conclusionsAnti-TL1A agents appear to be a promising therapeutic option in patients with IBD. Overall, anti-TL1A demonstrated an acceptable short-term safety profile, although mild adverse events were reported in almost half of treated patients.

Indexed as

AfimkibartDuvakitugInflammatory bowel diseasePF-06480605RO7790121Tulisokibart

Identifiers

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.