An Eight-Gene Blood Expression Profile Predicts the Response to Infliximab in Rheumatoid Arthritis

被引:80
作者
Julia, Antonio
Erra, Alba
Palacio, Carles
Tomas, Carlos
Sans, Xavier
Barcelo, Pere
Marsal, Sara
机构
[1] Grup de Recerca de Reumatologia, Institut de Recerca Hospital Universitari Vall d'Hebron, Barcelona
[2] Unitat d'Hematologia, Hospital Universitari Vall d'Hebron, Barcelona
来源
PLOS ONE | 2009年 / 4卷 / 10期
关键词
TUMOR-NECROSIS-FACTOR; REGULATORY T-CELLS; TNF-ALPHA THERAPY; MONOCLONAL-ANTIBODY; MICROARRAY DATA; DISEASE; CANCER; POPULATION; VALIDATION; SIGNATURE;
D O I
10.1371/journal.pone.0007556
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Background: TNF 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 Findings: We 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). Conclusions: The 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.
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页数:8
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