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Infliximab treatment in pediatric IBD is associated with specific microbial shifts rather than uniform diversity recoveryInfliximab Treatment Linked to Specific Gut Bacteria in Children

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Key Takeaway
Note that infliximab is linked to specific beneficial taxa enrichment rather than consistent overall microbial diversity gains.

This systematic review evaluates the relationship between infliximab (IFX) treatment and microbiome features in 242 pediatric patients with inflammatory bowel disease. The authors synthesize findings regarding alpha diversity, beta-diversity patterns, taxonomic profiles, and functional analyses to determine how microbial changes correlate with clinical outcomes.

Key findings indicate that while alpha diversity remains variable across studies, beta-diversity, taxonomic profiles, and functional analyses more consistently show positive IFX-associated microbial changes. Specifically, treatment responders frequently showed enrichment of beneficial taxa including Faecalibacterium, Subdoligranulum, and Bifidobacterium. Conversely, non-responders tended toward dysbiotic signatures, such as increased levels of Gammaproteobacteria and Candida. Functional and metabolomic studies post-IFX suggested beneficial shifts in bile-acid metabolism, short-chain fatty acid-related pathways, and inflammatory signaling.

A notable limitation identified is that clinical and biochemical improvements with IFX are not always accompanied by a uniform recovery of overall microbial diversity. These findings suggest that while IFX impacts specific microbial functions and compositions, these features are not currently established as definitive predictors for treatment response. Clinical utility remains limited by the lack of consistent diversity recovery despite successful therapy.

How this fits prior evidence

This systematic review addresses a gap in understanding how infliximab influences the microbiome specifically in pediatric populations with inflammatory bowel disease. While prior coverage has identified biomarkers like FABP2 for mucosal injury and explored pharmacological interventions such as GLP-1 receptor agonists to reduce systemic inflammation, this study focuses on the specific microbial shifts associated with IFX. It clarifies that clinical improvement does not always correlate with broad diversity recovery, providing a more nuanced view of how biological markers relate to treatment response in IBD.

Researchers looked at how the medication infliximab affects the gut microbiome in 242 children with inflammatory bowel disease. The study aimed to see if certain types of bacteria and metabolic pathways changed based on how well a child responded to the treatment.

Patients who responded well to the medicine often showed an increase in beneficial bacteria, such as Faecalibacterium, Subdoligranulum, and Bifidobacterium. In contrast, patients who did not respond well tended to have more of certain types of microbes like Gammaproteobacteria and Candida. The study also found that the treatment was linked to positive changes in how the body processes bile acids and short-chain fatty acids.

While many children saw clinical improvements with the medication, their overall microbial diversity did not always recover uniformly. Because these results come from a systematic review of existing data, they show a link between the medicine and specific gut bacteria rather than a guaranteed prediction for every patient. More research is needed to determine how these findings can help doctors choose the best treatment plans.

What this means for you:
Infliximab is linked to specific beneficial gut bacteria in children who respond well to the treatment.

Common questions

What did the study find about the gut microbiome and infliximab?

The review of 242 pediatric patients found that infliximab was linked to specific changes in microbial composition. While overall diversity did not always recover, those who responded well to treatment showed more beneficial bacteria like Faecalibacterium and Bifidobacterium.

Are there different results for children who do not respond to the medicine?

Yes, patients who did not respond to infliximab tended to show signs of an unbalanced microbiome. These individuals often had higher levels of Gammaproteobacteria and Candida compared to those who saw clinical improvement.

Does this mean the gut microbiome can predict if a child will get better?

The study shows a link between certain bacteria and treatment success, but these features are not yet definitive predictors for every patient. Because results vary, you should talk to a doctor about how these findings apply to specific cases.

Study Details

Study typeMeta analysis
EvidenceLevel 1
PublishedJul 2026
View Original Abstract ↓
BackgroundInfliximab (IFX) is a chimeric monoclonal antibody against tumor necrosis factor-alpha (TNF-α) that is widely used for induction and maintenance therapy in pediatric inflammatory bowel disease (IBD), yet its effects on the developing intestinal microbiome and treatment response remain unclear.ObjectiveTo systematically synthesize evidence on IFX-associated microbiome changes in pediatric IBD and evaluate microbiome features linked to treatment response.MethodsA systematic review was conducted following the PRISMA 2020 guidelines. PubMed, Scopus, Embase, and CENTRAL were searched from database inception until March 2026, and our results were synthesized narratively.ResultsOf the 945 records identified, 13 studies met the inclusion criteria, comprising 242 pediatric patients. Findings for alpha diversity were variable across studies. In contrast, beta-diversity patterns, taxonomic profiles, and functional analyses more consistently showed positive IFX-associated microbial changes. Responders to treatment more frequently showed enrichment of beneficial taxa, including Faecalibacterium, Subdoligranulum, and Bifidobacterium, while non-responders exhibited a tendency towards dysbiotic microbial signatures, evidenced by increased levels of Gammaproteobacteria and Candida. Functional and metabolomic studies suggested beneficial shifts in bile-acid metabolism, short-chain fatty acid-related pathways, and inflammatory signaling post IFX treatment. Clinical and biochemical improvements with IFX were consistently reported; however, these improvements were not always accompanied by uniform recovery of overall microbial diversity.ConclusionIn pediatric IBD, IFX is more consistently associated with shifts in microbial composition and function than with broad increases in overall microbial diversity. Further large, standardized studies are warranted to refine the role of microbiome features in biologic treatment stratification.Systematic Review Registrationhttps://www.crd.york.ac.uk/PROSPERO/view/CRD420251133625, identifier CRD420251133625.
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