Anti-Adalimumab Antibodies Purified from Juvenile Idiopathic Arthritis Patients: Kinetic Characterization Among Biosimilars
- PMID: 40422017
- PMCID: PMC12110412
- DOI: 10.3390/bios15050278
Anti-Adalimumab Antibodies Purified from Juvenile Idiopathic Arthritis Patients: Kinetic Characterization Among Biosimilars
Abstract
The use of adalimumab biosimilars has become increasingly common in clinical practice, reflecting their growing acceptance and efficacy as therapeutic alternatives to reference biologics. However, studies investigating the molecular interactions between anti-adalimumab antibodies (AAA) elicited in patients and different adalimumab biosimilars remain limited. This study aims to characterize the kinetic interactions between purified AAA from pediatric patients with Juvenile Idiopathic Arthritis and three adalimumab formulations: the originator Humira®, and the biosimilars GP2017 (Hyrimoz®) and SB5 (Imraldi®). For this purpose, adalimumab formulations were immobilized on a gold chip, and purified AAA were flowed to perform further kinetic analysis using the surface plasmon resonance (SPR) technology. Results showed that the KD values for purified AAA from patients treated with biosimilars GP2017 (Hyrimoz®) or SB5 (Imraldi®) were comparable across all formulations tested, including the originator Humira®. AAA interacted with Humira®, Hyrimoz®, and Imraldi® with similar apparent affinity (10-9 M > KD > 10-10 M); slight variations have been observed among patients, less among biosimilars. The similarity in KD values across biosimilars and the originator supports the notion that, at the level of immunogenicity, biosimilars can be considered clinically comparable to the originator.
Keywords: adalimumab; anti-drug antibodies; biosimilars; juvenile idiopathic arthritis; surface plasmon resonance.
Conflict of interest statement
The authors declare no conflicts of interest.
Figures




Similar articles
-
Comparative effectiveness of two adalimumab biosimilars in 1318 real-world patients with inflammatory rheumatic disease mandated to switch from originator adalimumab: nationwide observational study emulating a randomised clinical trial.Ann Rheum Dis. 2021 Nov;80(11):1400-1409. doi: 10.1136/annrheumdis-2021-219951. Epub 2021 Apr 29. Ann Rheum Dis. 2021. PMID: 33926921
-
Efficacy and Safety of Adalimumab Biosimilars: Current Critical Clinical Data in Rheumatoid Arthritis.Front Immunol. 2021 Apr 6;12:638444. doi: 10.3389/fimmu.2021.638444. eCollection 2021. Front Immunol. 2021. PMID: 33889152 Free PMC article. Review.
-
Navigating adalimumab biosimilars: an expert opinion.J Comp Eff Res. 2023 Nov;12(11):e230117. doi: 10.57264/cer-2023-0117. Epub 2023 Oct 19. J Comp Eff Res. 2023. PMID: 37855223 Free PMC article. Review.
-
Effectiveness of Adalimumab Biosimilars and Originator for Psoriasis.JAMA Dermatol. 2025 Apr 1;161(4):358-366. doi: 10.1001/jamadermatol.2025.0055. JAMA Dermatol. 2025. PMID: 40042863
-
Comparison of Performances of Adalimumab Biosimilars SB5, ABP501, GP2017, and MSB11022 in Treating Patients with Inflammatory Bowel Diseases: A Real-Life, Multicenter, Observational Study.Inflamm Bowel Dis. 2023 Mar 1;29(3):376-383. doi: 10.1093/ibd/izac092. Inflamm Bowel Dis. 2023. PMID: 35579320
References
-
- GaBI Journal Editor Patent Expiry Dates for Biologicals: 2018 Update. GaBI J. 2019;8:24–31. doi: 10.5639/gabij.2019.0801.003. - DOI
-
- Biosimilar Medicines: Overview | European Medicines Agency (EMA) [(accessed on 7 October 2024)]. Available online: https://www.ema.europa.eu/en/human-regulatory-overview/biosimilar-medici....
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical