RT Journal Article SR Electronic T1 Targeting early changes in the synovial microenvironment: a new class of immunomodulatory therapy? JF Annals of the Rheumatic Diseases JO Ann Rheum Dis FD BMJ Publishing Group Ltd and European League Against Rheumatism SP 186 OP 191 DO 10.1136/annrheumdis-2018-214294 VO 78 IS 2 A1 Aungier, Susan R A1 Cartwright, Alison J A1 Schwenzer, Anja A1 Marshall, Jennifer L A1 Dyson, Michael R A1 Slavny, Peter A1 Parthiban, Kothai A1 Karatt-Vellatt, Aneesh A1 Sahbudin, Ilfita A1 Culbert, Eric A1 Hextall, Patrick A1 Clanchy, Felix IL A1 Williams, Richard A1 Marsden, Brian D A1 Raza, Karim A1 Filer, Andrew A1 Buckley, Christopher Dominic A1 McCafferty, John A1 Midwood, Kim S YR 2019 UL http://ard.bmj.com/content/78/2/186.abstract AB Objectives Controlled immune responses rely on integrated crosstalk between cells and their microenvironment. We investigated whether targeting proinflammatory signals from the extracellular matrix that persist during pathological inflammation provides a viable strategy to treat rheumatoid arthritis (RA).Methods Monoclonal antibodies recognising the fibrinogen-like globe (FBG) of tenascin-C were generated by phage display. Clones that neutralised FBG activation of toll-like receptor 4 (TLR4), without impacting pathogenic TLR4 activation, were epitope mapped by crystallography. Antibodies stained synovial biopsies of patients at different stages of RA development. Antibody efficacy in preventing RA synovial cell cytokine release, and in modulating collagen-induced arthritis in rats, was assessed.Results Tenascin-C is expressed early in the development of RA, even before disease diagnosis, with higher levels in the joints of people with synovitis who eventually developed RA than in people whose synovitis spontaneously resolved. Anti-FBG antibodies inhibited cytokine release by RA synovial cells and prevented disease progression and tissue destruction during collagen-induced arthritis.Conclusions Early changes in the synovial microenvironment contribute to RA progression; blocking proinflammatory signals from the matrix can ameliorate experimental arthritis. These data highlight a new drug class that could offer early, disease-specific immune modulation in RA, without engendering global immune suppression.