Abstract

BackgroundTNF alpha blockade agents like infliximab are actually the treatment of choice for those rheumatoid arthritis (RA) patients who fail standard therapy. However, a considerable percentage of anti-TNF alpha treated patients do not show a significant clinical response. Given that new therapies for treatment of RA have been recently approved, there is a pressing need to find a system that reliably predicts treatment response. We hypothesized that the analysis of whole blood gene expression profiles of RA patients could be used to build a robust predictor to infliximab therapy.Methods and FindingsWe performed microarray gene expression analysis on whole blood RNA samples from RA patients starting infliximab therapy (n = 44). The clinical response to infliximab was determined at week 14 using the EULAR criteria. Blood cell populations were determined using flow cytometry at baseline, week 2 and week 14 of treatment. Using complete cross-validation and repeated random sampling we identified a robust 8-gene predictor model (96.6% Leave One Out prediction accuracy, P = 0.0001). Applying this model to an independent validation set of RA patients, we estimated an 85.7% prediction accuracy (75–100%, 95% CI). In parallel, we also observed a significantly higher number of CD4+CD25+ cells (i.e. regulatory T cells) in the responder group compared to the non responder group at baseline (P = 0.0009).ConclusionsThe present 8-gene model obtained from whole blood expression efficiently predicts response to infliximab in RA patients. The application of the present system in the clinical setting could assist the clinician in the selection of the optimal treatment strategy in RA.

Highlights

  • Rheumatoid Arthritis (RA) is one of the most prevalent autoimmune diseases in the world and is characterized by the chronic inflammation of the synovial joints

  • The present 8-gene model obtained from whole blood expression efficiently predicts response to infliximab in rheumatoid arthritis (RA) patients

  • Patients From January 2005 to June 2007, those RA patients with active disease (i.e. defined as a Disease Activity Score (DAS28) .3.2) from the Rheumatology Unit of the Hospital Universitari Vall d’Hebron (Barcelona, Spain) that were going to start infliximab therapy were considered for inclusion in the present study

Read more

Summary

Introduction

Rheumatoid Arthritis (RA) is one of the most prevalent autoimmune diseases in the world and is characterized by the chronic inflammation of the synovial joints. The origin of the disease is unknown but it is accepted that it is caused by the complex interaction of a genetic susceptibility background and environmental factors [2,3]. This lack of knowledge, has not prevented the development of pharmacological treatments that can efficiently control the progression of the disease. Like the other two approved anti-TNF blockers, adalimumab and etanercept, infliximab has proven to be an efficacious treatment for disease activity control in patients with RA [1]. TNF alpha blockade agents like infliximab are the treatment of choice for those rheumatoid arthritis (RA) patients who fail standard therapy. We hypothesized that the analysis of whole blood gene expression profiles of RA patients could be used to build a robust predictor to infliximab therapy

Methods
Results
Discussion
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call