Antiangiogenic effects of anti–tumor necrosis factor α therapy with infliximab in psoriatic arthritis

Abstract

Objective Neovascularization, with an increased number of synovial vessels with a characteristic morphology, seems to contribute to the progression of psoriatic arthritis (PsA). Accordingly, angiogenesis may be an important therapeutic target in PsA. The aim of this study was to analyze the effects of infliximab on angiogenesis in the synovial membrane of patients with PsA who responded to this therapy. Methods The study group comprised 9 patients with PsA who were selected for the presence of active polyarthritis (including knee synovitis) despite methotrexate therapy. Clinical and biologic evaluations were performed at each visit. Arthroscopy and synovial biopsies were performed at week 0, before infliximab therapy was initiated, and at week 8, after administration of 3 intravenous infusions of infliximab (5 mg/kg). We used immunohistochemistry to identify changes in infiltrating cells and in the angiogenesis modulators αvβ3 integrin, vascular endothelial growth factor (VEGF), angiopoietin 2 (Ang‐2), flt‐1 (VEGF receptor 1 [VEGFR‐1]), kinase insert domain receptor [KDR]/flk‐1 (VEGFR‐2), and stromal cell–derived factor 1 (SDF‐1). Neovascularization was assessed by automated histomorphometry of CD31+ vessels and by measuring αvβ3 expression. Results Rapid and significant clinical and biological improvement were observed after treatment in all patients. In the synovium, infliximab therapy induced a significant reduction in macrophages, the CD31+ vascular area, αvβ3+ neovessels/Ulex europaeus agglutinin+ vessels, VEGF and its receptor KDR/flk‐1 (VEGFR‐2), and SDF‐1+ vessels. Expression of flt‐1 (VEGFR‐1), and SDF‐1 in lining cells showed a nonsignificant reduction, whereas expression of Ang‐2 increased. In 3 patients, reverse transcription–polymerase chain reaction confirmed the changes in some of these markers at the messenger RNA level. Conclusion These results show consistent changes in several factors involved in angiogenesis regulation, in parallel with the clinical response to infliximab in patients with PsA. The pattern of reduced VEGF with increased Ang‐2 suggests vascular regression as a potential mechanism underlying the antiangiogenic effect of infliximab.