Influence of immunogenicity on the efficacy of longterm treatment of spondyloarthritis with infliximab

Background Infliximab (IFX) is a monoclonal antibody against tumour necrosis factor α that is effective for treating spondyloarthritis (SpA). However, after initial success of the drug some patients lose responsiveness or develop infusion reactions, which may be related to the development of antibod...

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Veröffentlicht in:Annals of the rheumatic diseases 2012-12, Vol.71 (12), p.1955-1960
Hauptverfasser: Plasencia, Chamaida, Pascual-Salcedo, Dora, Nuño, Laura, Bonilla, Gema, Villalba, Alejandro, Peiteado, Diana, Díez, Jesús, Nagore, Daniel, del Agua, Ainhoa Ruiz, Moral, Rosario, Martin-Mola, Emilio, Balsa, Alejandro
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Sprache:eng
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Zusammenfassung:Background Infliximab (IFX) is a monoclonal antibody against tumour necrosis factor α that is effective for treating spondyloarthritis (SpA). However, after initial success of the drug some patients lose responsiveness or develop infusion reactions, which may be related to the development of antibodies against the drug. Objective To investigate the clinical relevance of antibodies to infliximab (ATI) formation in patients with SpA undergoing IFX treatment over a prolonged period. Methods 94 patients with SpA treated with IFX from 1999 to 2010 were studied. Their clinical characteristics, serum trough IFX levels and ATI status were evaluated for a mean of 6.99 (95% CI:6.28 to 7.7) years. Clinical activity and improvement were measured using the Ankylosing Spondylitis Disease Activity Score (ASDAS): inactive 4 years). Results ATI were detected in 24 (25.5%) patients. The patients with ATI had higher ASDAS scores than those without ATI (2.55±0.89 vs 1.79±1.04, p=0.038 at 6 months; 1.95±0.67 vs 1.67±0.71, p=0.042 at 1 year; 2.52±0.99 vs 1.53±0.81, p=0.024 at >4 years). Eleven patients (12%) developed infusion-related reactions, and of these, ATI were present in eight patients (73%). The patients with infusion-related reactions had higher ATI titres (median 12 931 AU/ml, IQR 853–82 437) vs median 2454 AU/ml, IQR 449–7718, p=0.028) and shorter survival (4.25 years vs 8.19 years, p
ISSN:0003-4967
1468-2060
DOI:10.1136/annrheumdis-2011-200828