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Abstract Number: 147

Modular Analysis Of In Peripheral Blood Gene Expression In Rheumatoid Arthritis Captures Reproducible Gene Expression Changes In TNF Responders

Mark Curran1, Michaela Oswald2, Sarah Lamberth1, Carrie Brodmerkel1, Zhenya Cherkas1 and Peter K. Gregersen3, 1Janssen Research & Development, LLC., Spring House, PA, 2Laboratory of Genomics and Human Genetics, The Feinstein Institute for Medical Research, Manhasset, NY, 3Genomics and Human Genetics, Feinstein Institute for Medical Research, Manhasset, NY

Meeting: 2013 ACR/ARHP Annual Meeting

Keywords: Gene Expression and rheumatoid arthritis (RA)

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Session Information

Title: Genetics and Genomics of Rheumatic Disease I

Session Type: Abstract Submissions (ACR)

Background/Purpose: The use of whole blood gene expression to predict and follow the response to TNF inhibition therapy in RA has been challenging due to the complex nature of the data.

Methods: Here we employ an approach to gene expression analysis that is based on gene expression “modules” previously reported by Chassubel (Immunity 2:150-64, 2008). Whole blood RNA (PAXgene) was obtained at baseline and 12 or 14 weeks on two cohorts of rheumatoid arthritis patients beginning anti-TNF therapy.

Results: The initial cohort was enrolled by the ABCoN and contains 50 subjects stratified by EULAR Good Responders (N=14), Moderate Responders (N=21) and Non Responders (N=15) at 12 weeks after starting therapy.  Good and Moderate Responders exhibited highly significant changes in multiple modules using a hypergeometric analysis. These included dramatic decreases in modules related to the myeloid lineage and inflammation, along with increases in B cell and plasma cell modules as well as in a number of modules related to the MHC and ribosomal proteins and other “undefined” module groups. Strikingly, Non Responders exhibited very little change in any modules. We have replicated these data in patients enrolled in a clinical trial of Simponi®, with full expression data available on 29 Good Responders, and 37 Moderate Responders. We observed nearly identical modular changes to those identified in the ABCoN Responders after 14 weeks of treatment. Only 6 Non Responders were available for study in this dataset, making convincing replication difficult for this subgroup. Several other replication datasets are currently being analyzed. 

Conclusion: These data suggest that using gene expression modules related to inflammatory disease may provide a valuable method of characterizing the responder status of RA patients treated with TNF inhibitors or other biologic therapies.


Disclosure:

M. Curran,

Janssen Research & Development, LLC.,

3;

M. Oswald,
None;

S. Lamberth,

Janssen Research & Development, LLC.,

3;

C. Brodmerkel,

Janssen Research & Development, LLC.,

3;

Z. Cherkas,

Janssen Pharmaceutica Product, L.P.,

3;

P. K. Gregersen,

Janssen Pharmaceutica Product, L.P.,

2.

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ACR Meeting Abstracts - https://acrabstracts.org/abstract/modular-analysis-of-in-peripheral-blood-gene-expression-in-rheumatoid-arthritis-captures-reproducible-gene-expression-changes-in-tnf-responders/

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