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Updated: May 25, 2026

An Immunohistopathologic Study to Profile the Folate Receptor Beta Macrophage and Vascular Immune Microenvironment in Giant Cell Arteritis
Published on: February 8, 2019
Efficacy of tocilizumab in refractory giant cell arteritis
Julien Vinit1, Philip Bielefeld, Géraldine Muller
1Service de médecine interne et maladies systémiques, hôpital Général, University Hospital of Dijon, 3, rue Faubourg-Raines, 21033 Dijon cedex, France. julien.vinit@chu-dijon.fr
Insights
Giant cell arteritis (GCA) treatment can be challenging. An interleukin-6 blocker, tocilizumab, effectively treated a refractory GCA case with bowel involvement, reducing steroid dependence.
Area of Science:
- Rheumatology
- Immunology
- Gastroenterology
Background:
- Giant cell arteritis (GCA) is the most common vasculitis, posing a high risk of vascular thrombosis and ischemic complications like blindness.
- Current treatments, primarily long-term corticosteroids, have significant side effects, and other immunosuppressants show limited efficacy in reducing steroid use.
- Th17 lymphocytes and interleukin-6 (IL-6) are implicated in GCA pathogenesis.
Observation:
- A rare case of refractory GCA involving the ileum (bowel) was reported in a patient dependent on high-dose steroids and methotrexate for two years.
- The patient received tocilizumab, an interleukin-6 (IL-6) blocker.
Findings:
- Tocilizumab treatment led to sustained remission of GCA symptoms for at least six months.
- The patient was able to significantly decrease corticosteroid dosage without experiencing a relapse.
Implications:
- Interleukin-6 (IL-6) blockade represents a promising therapeutic strategy for refractory giant cell arteritis (GCA), particularly cases with gastrointestinal involvement.
- Targeting the IL-6 pathway may offer an effective alternative to reduce long-term corticosteroid dependence and associated toxicities in GCA patients.
- This case highlights the potential of IL-6 inhibitors in managing complex and treatment-resistant vasculitis cases.
Abstract:
Giant cell arteritis is the most frequent form of vasculitis characterized by a high risk of vascular thrombosis. Major complications are blindness and other vascular ischemia but bowel ischemic involvement is rare. Treatment is based on long-term steroid therapy with numerous side effects. The efficacy of immunosuppressive drugs like azathioprine methotrexate or anti-tumor necrosis factor antibodies appears to be too low to reduce the use of steroids. Th17 lymphocytes and interleukin-6 play an important role in pathogenesis of giant cell arteritis. We report here a case of effective interleukin-6 blocker in the treatment of refractory giant cell arteritis with ileitis and high-dose steroid dependence despite 2 years of treatment with steroids and methotrexate. After infusions of tocilizumab, no relapse at 6 months was found despite the decrease in corticosteroids.
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