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Modification of Pro- and Antiinflammatory Cytokines and Vascular-Related Molecules by Tumor Necrosis Factor-a Blockade in Patients with Rheumatoid Arthritis

INMACULADA MACÍAS, SERGIO GARCÍA-PÉREZ, MAR RUIZ-TUDELA, FERMÍN MEDINA, NICOLÁS CHOZAS, and JOSÉ A. GIRÓN-GONZÁLEZ

ABSTRACT.

Objective. Analysis of serum concentrations and modifications of tumor necrosis factor-a (TNF-a), its soluble receptors (TNFR), interleukin 10 (IL-10), and vascular related molecules [soluble vascular cell adhesion molecule 1 (sVCAM-1), vascular endothelial growth factor (VEGF)] after therapy with methotrexate (MTX) and anti-TNF (infliximab) in patients with rheumatoid arthritis (RA).

Methods. Thirty-six patients with RA and 20 healthy controls were included. Patients had been orally taking a stable dose of MTX of at least 12.5 mg/week for a minimum of 6 months before inclusion in the study. Twenty-five patients had shown a clinical response to MTX (MTX Group). The other 11 had shown an unsatisfactory response and presented with active RA; they were selected for additional treatment with infliximab (MTX + IFM Group). Disease activity score (DAS28), hemoglobin concentration, erythrocyte sedimentation rate (ESR), C-reactive protein (CRP), and serum levels of TNF-a, soluble TNFR, IL-10, sVCAM-1 and VEGF were determined at baseline and prior to every infusion of infliximab (3 mg/kg) at 2, 6, 14, 22, and 30 weeks.

Results. Although serum levels of TNF-a were similar in patients and controls, patients showed significantly higher concentrations of both soluble TNFR (sTNFR55 and sTNFR75), IL-10, sVCAM-1, and VEGF than healthy individuals. Significantly higher levels of sVCAM-1 and VEGF, but not of the other tested molecules, were detected in those with active disease. After infliximab treatment (MTX + IFM Group) there was a significant decrease in DAS28 and modified Health Assessment Questionnaire scores and ESR and CRP levels. Serum concentration of VEGF showed a significant decrease after infliximab, with levels comparable to those of patients with inactive RA, although VEGF continued to present higher values than in healthy controls.

Conclusion. Increased levels of vascular related molecules sVCAM-1 and VEGF are serum markers of active RA. The absence of normalization of levels of these molecules in patients with inactive RA could be one of the reasons response to therapy is only temporary. (J Rheumatol 2005;32:2102-8)

Key Indexing Terms:

RHEUMATOID ARTHRITIS
ANTI-TUMOR NECROSIS FACTOR-a

TUMOR NECROSIS FACTOR-a
VASCULAR ENDOTHELIAL GROWTH FACTOR 1
VASCULAR CELL ADHESION MOLECULE 1
INTERLEUKIN 10


From the Rheumatology Service and Internal Medicine Service, Hospital Universitario Puerta del Mar, Cádiz, Spain.

I. Macías, MD, PhD; S. García-Pérez, MD, PhD; M. Ruiz-Tudela, MD; F. Medina, MD; N. Chozas, MD, PhD; J.A. Girón-González, MD, PhD.

Address reprint requests to Dr. J.A. Girón González, Servicio de Medicina Interna, Hospital Universitario "Puerta del Mar," avda. Ana de Viya 21, 11009 Cádiz, Spain. E-mail: joseantonio.giron@uca.es

Accepted for publication June 24, 2005.




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