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Updated: Sep 27, 2025

An Immunohistopathologic Study to Profile the Folate Receptor Beta Macrophage and Vascular Immune Microenvironment in Giant Cell Arteritis
Published on: February 8, 2019
Treatment of Giant Cell Arteritis (GCA)
Alexis Régent1,2, Luc Mouthon1,2
1Service de Médecine Interne, Centre de Référence Maladies Auto-Immunes et Systémiques Rares d'Ile de France, APHP-CUP, Hôpital Cochin, F-75014 Paris, France.
Insights
Giant cell arteritis (GCA) treatment is evolving beyond glucocorticoids (GCs). New biologic therapies targeting specific pathways show promise for improving outcomes and reducing GC toxicity in patients over 50.
Area of Science:
- Rheumatology
- Immunology
- Internal Medicine
Background:
- Giant cell arteritis (GCA) is the most common large-vessel vasculitis in individuals over 50.
- Glucocorticoids (GCs) are the primary treatment but are associated with significant adverse events in this population.
- Limited efficacy of traditional immunosuppressants necessitates exploring novel therapeutic strategies.
Purpose of the Study:
- To review the scientific rationale for emerging targeted therapies in GCA.
- To discuss the therapeutic strategies and optimal application of these new agents.
- To evaluate the potential of biologics in improving GCA management and reducing GC burden.
Main Methods:
- Review of current literature on GCA pathophysiology and treatment.
- Analysis of clinical trial data for novel therapeutic agents.
- Discussion of the benefit/risk profiles of various treatment options.
Main Results:
- Tocilizumab (anti-IL-6 receptor inhibitor) has demonstrated significant benefits in reducing GC dosage and preventing relapses.
- Several other targeted therapies, including anti-IL-12/23, anti-IL-17, and JAK inhibitors, are under investigation.
- Mavrilimumab, ustekinumab, and abatacept have shown promising results in Phase 2 trials.
Conclusions:
- While significant progress has been made, the optimal use of each new therapy for GCA requires further definition.
- Targeted therapies offer potential for improved efficacy and safety compared to traditional treatments.
- Future research should focus on defining specific indications and treatment strategies for novel GCA therapies.
Abstract:
Giant cell arteritis (GCA) is the most frequent primary large-vessel vasculitis in individuals older than 50. Glucocorticoids (GCs) are considered the cornerstone of treatment. GC therapy is usually tapered over months according to clinical symptoms and inflammatory marker levels. Considering the high rate of GC-related adverse events in these older individuals, immunosuppressive treatments and biologic agents have been proposed as add-on therapies. Methotrexate was considered an alternative option, but its clinical impact was limited. Other immunosuppressants failed to demonstrate a significant favourable benefit/risk ratio. The approval of tocilizumab, an anti-interleukin 6 (IL-6) receptor inhibitor brought significant improvement. Indeed, tocilizumab had a noticeable effect on cumulative GCs' dose and relapse prevention. After the improvement in pathophysiological knowledge, other targeted therapies have been proposed, with anti-IL-12/23, anti-IL-17, anti-IL-1, anti-cytotoxic T-lymphocyte antigen 4, Janus kinase inhibitors or anti-granulocyte/macrophage colony stimulating factor therapies. These therapies are currently under evaluation. Interestingly, mavrilimumab, ustekinumab and, to a lesser extent, abatacept have shown promising results in phase 2 randomised controlled trials. Despite this recent progress, the value, specific condition and optimal application of each treatment remain undecided. In this review, we discuss the scientific rationale for each treatment and the therapeutic strategy.
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