Immunogenicity of antitumor necrosis factor therapy in patients with spondyloarthritis
-
Ines Mahmoud
, Leila Rouached, Aicha Ben Tekaya
, Olfa Saidane , Selma Bouden , Saoussen Jradi , Imen Sfar , Rawdha Tekaya , Kawther Ben Abdelghani , Yousr Lakhoua Gorgi and Leila Abdelmoula
Abstract
Objectives
To evaluate the serum dosage of the biomedicine (DBM) and the incidence of antidrug antibody (ADA) against antitumor necrosis factor (TNF) in spondyloarthritis, and to demonstrate the influence of these parameters on the clinical efficiency.
Methods
We conducted a cross-sectional multicentric study including patients with spondylarthritis (SpA) under antiTNF (infliximab [INF], etanercept [ETA] and adalimumab [ADL]) for at least 6 months. A dosage of the ADA and DBM were practiced by the immuno-enzymatic essay.
Result
Seventy one patients were recruited. Disease modifying antirheumatic drugs (DMARDs) were associated with anti-TNF in 30%. ADA was positive in 54% for INF, 33% for ADL and 0% for ETA with a significant difference(p<0.0001). Immunogenicity was correlated to a bad therapeutic response (Bath Ankylosing Spondylitis Disease Activity Index [BASDAI]≥4)(p=0.04). The DBM was inversely correlated with the rate of ADA for patients treated with INF(p<0.0001) and ADL(p<0.0001). The DBM was also inversely correlated with BASDAI of INF(p=0.03) and ADL (p=0.01). ADA was significantly associated with an anterior switch of anti TNF(p=0.04), the use of INF(p=0.002), presence of coxitis(p=0.01) and higher body mass index (BMI)(p=0.007). DMARDs associated with anti TNF were not a protective factor for positive ADA. In a multivariate study, only INF and BMI were independent factors of positive ADA.
Conclusion
The ADA formation lowered the DBM and favored the therapeutic failure.
Acknowledgments
We thank the departments of rheumatology for assistance, access to patients and for comments that greatly improved the manuscript. We would also like to show our gratitude to the department of immunology for facilitating the blood collection and fast results during this research
Research funding: None declared.
Author contributions: All authors have accepted responsibility for the entire content of this manuscript and approved its submission.
Competing interests: Authors state no conflict of interest.
Informed consent: Informed consent was obtained from all individuals included in this study.
Ethical approval: Our study complies with the Declaration of Helsinki. Our locally appointed ethics committee has approved the research protocol and informed consent has been obtained from the subjects.
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Articles in the same Issue
- Frontmatter
- Review
- Herbal approach for the management of C0VID-19: an overview
- Original Articles
- Clinically important drug–drug interactions in patients admitted to hospital with COVID-19: drug pairs, risk factors, and management
- Spinal and general anesthesia produces differential effects on oxidative stress and inflammatory cytokines in orthopedic patients
- Immunogenicity of antitumor necrosis factor therapy in patients with spondyloarthritis
- Biochip-based approach for comprehensive pharmacogenetic testing
- Clinical efficacy of Majoon Falasfa and Roghan-e-Surkh in post-stroke-disability: an open labeled, pre-post analysis
- Ascorbic acid improves extrapyramidal syndromes and corpus striatal degeneration induced by dopamine-2 receptor inhibition in Wistar rats
- Rutin ameliorates scopolamine-induced learning and memory impairments through enhancement of antioxidant defense system and cholinergic signaling
- Adansonia digitata L. leaf extract attenuates lead-induced cortical histoarchitectural changes and oxidative stress in the prefrontal cortex of adult male Wistar rats