IgA rheumatoid factor as a serological predictor of poor response to tumour necrosis factor α inhibitors in rheumatoid arthritis

• Published in: International journal of rheumatic diseases Vol. 17; no. 8; pp. 872 - 877
• Main Authors: Sakthiswary, Rajalingham, Shaharir, Syahrul S., Mohd Said, Mohd S., Asrul, Abdul W., Shahril, Nor S.
• Format: Journal Article
• Language: English
• Published: England Blackwell Publishing Ltd 01.11.2014
• Subjects: Adalimumab; Antibodies, Monoclonal - therapeutic use; Antibodies, Monoclonal, Humanized - therapeutic use; Arthritis, Rheumatoid - drug therapy; Arthritis, Rheumatoid - immunology; Etanercept; Female; Humans; IgA rheumatoid factor; Immunoglobulin A - blood; Immunoglobulin G - therapeutic use; Immunologic Factors - immunology; Immunologic Factors - therapeutic use; Infliximab; Male; Middle Aged; Prognosis; Receptors, Tumor Necrosis Factor - therapeutic use; rheumatoid arthritis; Rheumatoid Factor - immunology; Rheumatoid Factor - therapeutic use; rheumatoid factor isotypes; Tumor Necrosis Factor-alpha - antagonists & inhibitors; tumour necrosis factor α inhibitors; tumour necrosis factor α inhibitors; rheumatoid factor isotypes; rheumatoid arthritis; IgA rheumatoid factor
• ISSN: 1756-1841; 1756-185X; 1756-185X
• DOI: 10.1111/1756-185X.12443

Aim The main objective of this study is to elucidate the role of immunoglobulin A (IgA) rheumatoid factor (RF) in predicting the clinical response to tumour necrosis factor α inhibitors (TNFi) among patients with rheumatoid arthritis (RA). Method We recruited all patients with RA who were ever on TNFi for a minimum duration of 3 months at our centre. Based on the European League Against Rheumatism response criteria, subjects were further divided into responders and non‐responders. Age‐matched RA patients who were on conventional disease‐modifying anti‐rheumatic drugs and in remission were enrolled as controls. Subjects were tested for quantitative values of IgA, IgM, IgG RF and anti‐citrulinated cyclic peptides (CCP). Further, all subjects were assessed for the disease activity score that includes 28 joints (DAS28) and Stanford Health Assessment Questionnaire (HAQ) 8‐item Disability Index (HAQ‐DI). Results A total of 31 subjects with RA who had received TNFi and 15 controls were enrolled in this study. There was a trend for the non‐responders (n = 10) to have higher levels of all isotypes of RF and anti‐CCP. However, only the IgA RF and anti‐CCP levels were significantly higher in the non‐responder group compared to the responders and controls (P = 0.001, P = 0.034, respectively). On multivariate analysis, only the IgA RF remained significant (OR 0.989; 95% CI 0.980–0.999; P = 0.026). Conclusion IgA RF is potentially a novel predictor of response to TNFi in RA patients. Testing for pretreatment IgA RF levels could be a reasonable consideration before commencement of TNFi.