Praxis Medical Insights

Est. 2024 • Clinical Guidelines Distilled

Made possible by volunteer editors from the University of Calgary & University of Alberta

Last Updated: 11/14/2025

Shingles Vaccine and Rituximab Therapy

Introduction to Vaccine Administration

  • The American College of Rheumatology recommends administering the recombinant zoster vaccine (Shingrix) at least 2-4 weeks before initiating rituximab therapy, as rituximab profoundly impairs vaccine responses for 6-9 months after treatment 1, 2.

Vaccine Selection and Timing

  • The European League Against Rheumatism recommends using only the recombinant zoster vaccine (RZV/Shingrix), never the live zoster vaccine (ZVL/Zostavax) in patients who will receive or are receiving rituximab, due to the risk of vaccine-strain varicella dissemination 1, 2.
  • The recombinant vaccine has demonstrated significant T-cell responses even in patients with hematologic malignancies on anti-CD20 therapies, making it the safer and more effective choice 1, 2.

Optimal Timing for Vaccination

  • The American College of Rheumatology suggests that if a patient is already on rituximab, they should wait at least 6 months after the last dose (ideally 9-12 months when B-cell recovery is complete) before vaccinating, then delay the next rituximab dose by at least 4 weeks post-vaccination 5, 6.

Mechanistic Rationale for Vaccine Response

  • Rituximab causes profound B-cell depletion lasting 6-9 months, with full recovery typically occurring 9-12 months after therapy, severely hampering humoral antibody responses to vaccines during this period 4, 5, 6.

Clinical Context and Risk Assessment

  • Patients with autoimmune inflammatory rheumatic diseases have significantly increased risk of herpes zoster compared to the general population, which is further amplified by rituximab treatment itself 6, 7.

Post-Vaccination Monitoring and Safety

  • The National Comprehensive Cancer Network recommends measuring VZV-specific antibody titers 4 weeks after completing the vaccine series to confirm adequate response, and considering revaccination if titers are inadequate and rituximab has been discontinued for ≥9 months 3, 4.
  • The recombinant zoster vaccine is non-live and safe to administer to immunocompromised patients, and prophylactic antiviral therapy for herpes zoster may be considered in high-risk patients during rituximab treatment 1, 2, 8.