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Rheumatoid factors revisited in the age of biologic therapy
Ali Berkant Avci1, Eugen Feist2,3, Gerd R Burmester4
1Department of Internal Medicine, Rheumatology, Medical Park Antalya Hospital, Antalya, Türkiye.
Abstract:
The discovery of RF has been instrumental in diagnosing and classifying RA. Various RF isotypes, including IgM-RF and IgA-RF, have been linked to disease severity and treatment responses. The role of RF in RA pathogenesis, primarily through the formation of immune complexes, also carries the potential to influence the response to different medications. Recent progress in biologic therapies has further elucidated the role of RF in RA management. Treatments such as rituximab, abatacept and tocilizumab have shown differential efficacy based on RF status, with RF-positive patients often exhibiting better responses. Recent research also suggests that TNF inhibitors (TNFi) lacking the IgG1-Fc fragment like certolizumab pegol (CZP) may offer advantages over TNFi with an IgG1-Fc fragment, in RF-positive patients by preventing immune complex formation. Since this early observation is predominantly derived from previous multicentre studies with heterogeneous populations and potentially varying RF measurement methods, prospective randomized studies directly addressing this issue are essential for a more thorough and reliable evaluation. This paper is a narrative review outlining the evolving understanding of RF in the context of biologic therapies, emphasizing the need for personalized treatment approaches based on serological profiles and underlying immune mechanisms.
Insights
Rheumatoid factor (RF) influences rheumatoid arthritis (RA) treatment. RF-positive patients often respond better to biologics, but specific therapies like certolizumab pegol may offer advantages by preventing immune complex formation.
Area of Science:
- Immunology
- Rheumatology
- Pharmacology
Background:
- Rheumatoid factor (RF) is crucial for diagnosing and classifying rheumatoid arthritis (RA).
- Different RF isotypes (e.g., IgM-RF, IgA-RF) correlate with RA severity and treatment outcomes.
- RF's role in RA pathogenesis involves immune complex formation, impacting medication response.
Purpose of the Study:
- To review the evolving understanding of RF in the context of biologic therapies for RA.
- To highlight the need for personalized treatment strategies based on serological profiles.
Main Methods:
- Narrative review of existing literature on RF and biologic therapies in RA.
- Analysis of differential efficacy of biologics (rituximab, abatacept, tocilizumab) based on RF status.
- Exploration of TNF inhibitors (TNFi) with and without IgG1-Fc fragments in RF-positive RA.
Main Results:
- RF-positive patients generally show better responses to certain biologics.
- TNF inhibitors lacking IgG1-Fc (e.g., certolizumab pegol) may be advantageous in RF-positive RA by mitigating immune complex formation.
- Heterogeneity in past studies necessitates further prospective research.
Conclusions:
- RF status is a key factor in predicting response to biologic therapies in RA.
- Personalized medicine approaches considering serological profiles and immune mechanisms are essential for optimizing RA treatment.
- Further randomized studies are required to validate specific therapeutic strategies for RF-positive RA patients.
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