What is the recommended dose of infliximab (chimeric monoclonal antibody against tumor necrosis factor-alpha (TNF-alpha)) for a patient with vasculitis?

Medical Advisory BoardAll articles are reviewed for accuracy by our Medical Advisory Board
Educational purpose only • Exercise caution as content is pending human review
Article Review Status
Submitted
Under Review
Approved

Last updated: January 23, 2026View editorial policy

Personalize

Help us tailor your experience

Which best describes you? Your choice helps us use language that's most understandable for you.

Infliximab Dosing for Vasculitis

Infliximab is NOT a first-line agent for vasculitis and should only be considered for refractory or relapsing disease at a dose of 3-5 mg/kg per infusion, given every 1-2 months, though current guidelines prioritize rituximab or cyclophosphamide over infliximab for standard treatment. 1

Current Guideline Recommendations

The most recent KDIGO 2024 guidelines for ANCA-associated vasculitis do not include infliximab as a recommended therapy for induction or maintenance treatment. 1 Instead, the guidelines recommend:

  • First-line induction therapy: Rituximab (375 mg/m² weekly × 4 weeks) or cyclophosphamide (oral 2 mg/kg/day or IV 15 mg/kg at weeks 0,2,4,7,10,13) with glucocorticoids 1
  • Maintenance therapy: Rituximab or azathioprine with low-dose glucocorticoids for 18 months to 4 years 1
  • Refractory disease: Increase glucocorticoids, switch between rituximab and cyclophosphamide, or consider plasma exchange 1

Historical Use of Infliximab

When infliximab has been used for vasculitis (primarily in older literature), the dosing has been:

  • 3-5 mg/kg per infusion 1
  • Frequency: Every 1-2 months 1
  • Initial loading: Some protocols used infusions at weeks 0,2, and 6, then every 8 weeks 2, 3, 4

The 2009 EULAR guidelines listed infliximab only as an alternative option for relapsing, refractory, or persistent disease, not as standard therapy. 1

Critical Caveats and Contraindications

Infliximab should NOT be used for giant cell arteritis. A phase II trial demonstrated that patients receiving infliximab (5 mg/kg) had higher rates of disease activity and lower remission rates compared to placebo. 1 This represents a clear contraindication.

Infliximab can paradoxically cause vasculitis. Case reports document hypersensitivity vasculitis with leukocytoclastic vasculitis occurring after infliximab administration, even after the first dose. 5 This limits its utility as a vasculitis treatment.

Clinical Context for Modern Practice

In contemporary practice, infliximab has been largely supplanted by rituximab for refractory ANCA-associated vasculitis. The evidence supporting infliximab consists primarily of small open-label studies from 2002-2004 showing:

  • 88% remission rates in 32 patients with refractory disease 3
  • Mean BVAS reduction from 12.3 to 0.3 by week 14 3
  • However, 21% developed severe infections and 20% experienced disease flares despite continued therapy 3

For refractory ANCA-associated vasculitis in 2024-2025, rituximab (375 mg/m² IV weekly for 4 doses or 1000 mg on days 1 and 15) is the preferred alternative agent, not infliximab. 6

When Infliximab Might Be Considered

If infliximab is being considered (which should be rare), appropriate scenarios include:

  • Refractory disease after failure of rituximab and cyclophosphamide 1, 2, 3
  • Specific cases of Behçet's disease with severe ocular involvement (5 mg/kg at weeks 0,2,6, then every 8 weeks) 7
  • Patients enrolled in clinical trials 1

The higher dose of 5 mg/kg appears more effective than 3 mg/kg for inducing remission in the limited available data. 4

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

Have a follow-up question?

Our Medical A.I. is used by practicing medical doctors at top research institutions around the world. Ask any follow up question and get world-class guideline-backed answers instantly.