Multimodal Profiling of Peripheral Blood Identifies Proliferating Circulating Effector CD4+ T Cells as Predictors for Response to Integrin α4β7-Blocking Therapy in Inflammatory Bowel Disease
View abstract on PubMed
Summary
This summary is machine-generated.Predicting inflammatory bowel disease treatment response is crucial. A specific T-cell signature in nonresponders before vedolizumab therapy may predict treatment outcomes, aiding personalized medicine.
Area Of Science
- Immunology
- Gastroenterology
- Precision Medicine
Background
- Biological therapies like vedolizumab are effective for inflammatory bowel disease (IBD).
- Predicting patient response to IBD therapies remains a significant clinical challenge.
- Reliable biomarkers are needed to guide personalized treatment strategies for IBD.
Purpose Of The Study
- To identify predictors of treatment response to vedolizumab in IBD patients.
- To comprehensively assess vedolizumab-induced immunologic changes.
- To develop a predictive classifier for personalized IBD management.
Main Methods
- Prospective sampling of two IBD patient cohorts receiving vedolizumab.
- Multi-omic analysis including mass cytometry, scRNA-seq, BCR/TCR-seq, and proteomics.
- Machine learning integration of multimodal data to identify predictive signatures.
Main Results
- Vedolizumab induced significant alterations in circulating immune cell populations and T-cell receptor diversity.
- A distinct signature of proliferating CD4+ memory T cells was identified in nonresponders prior to treatment.
- This signature indicated an activated T-helper 1/T-helper 17 phenotype with elevated integrin α4β1.
Conclusions
- A reliable predictive classifier for vedolizumab response in IBD was identified.
- The findings have significant implications for personalizing IBD treatment strategies.
- Understanding T-cell phenotypes can guide future therapeutic development.
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