Research ArticleRheumatoid Arthritis
Plasma Levels of Eicosapentaenoic Acid Are Associated with Anti-TNF Responsiveness in Rheumatoid Arthritis and Inhibit the Etanercept-driven Rise in Th17 Cell Differentiation in Vitro
Louisa Jeffery, Helena L. Fisk, Philip C. Calder, Andrew Filer, Karim Raza, Christopher D. Buckley, Iain McInnes, Peter C. Taylor and Benjamin A. Fisher
The Journal of Rheumatology June 2017, 44 (6) 748-756; DOI: https://doi.org/10.3899/jrheum.161068
Louisa Jeffery
From the Rheumatology Research Group and Arthritis Research
UK Rheumatoid Arthritis Pathogenesis Centre of Excellence (RACE), University of Birmingham, Birmingham; Human Development and Health Academic Unit, Faculty of Medicine, University of Southampton;
UK National Institute for Health Research (NIHR) Southampton Biomedical Research Centre, University Hospital Southampton National Health Service (NHS) Foundation Trust; University of Southampton, Southampton; Glasgow Biomedical Research Centre, University of Glasgow, Glasgow; Kennedy Institute of Rheumatology, University of Oxford, Oxford,
UK.
Helena L. Fisk
Philip C. Calder
Andrew Filer
Karim Raza
Christopher D. Buckley
Iain McInnes
Peter C. Taylor
Benjamin A. Fisher
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In this issue
The Journal of Rheumatology
Vol. 44, Issue 6
1 Jun 2017
Plasma Levels of Eicosapentaenoic Acid Are Associated with Anti-TNF Responsiveness in Rheumatoid Arthritis and Inhibit the Etanercept-driven Rise in Th17 Cell Differentiation in Vitro
Louisa Jeffery, Helena L. Fisk, Philip C. Calder, Andrew Filer, Karim Raza, Christopher D. Buckley, Iain McInnes, Peter C. Taylor, Benjamin A. Fisher
The Journal of Rheumatology Jun 2017, 44 (6) 748-756; DOI: 10.3899/jrheum.161068
Plasma Levels of Eicosapentaenoic Acid Are Associated with Anti-TNF Responsiveness in Rheumatoid Arthritis and Inhibit the Etanercept-driven Rise in Th17 Cell Differentiation in Vitro
Louisa Jeffery, Helena L. Fisk, Philip C. Calder, Andrew Filer, Karim Raza, Christopher D. Buckley, Iain McInnes, Peter C. Taylor, Benjamin A. Fisher
The Journal of Rheumatology Jun 2017, 44 (6) 748-756; DOI: 10.3899/jrheum.161068