Current information about vaccination practice in pediatric rheumatic diseases and recommendations for future

Ceyhun Açarı1, Erbil Ünsal1

  • 1Division of Rheumatology, Department of Pediatrics, Dokuz Eylül University Faculty of Medicine, Izmir, Turkey.

Insights

Pediatric patients with rheumatic diseases need safe and effective immunizations due to increased infection risk from treatments like immunosuppressive drugs and biologics. Vaccination strategies must consider disease and treatment effects for optimal immune response and safety.

Area of Science:

  • Pediatric Rheumatology
  • Immunology
  • Vaccinology

Background:

  • Pediatric patients with autoinflammatory or rheumatic diseases face heightened infection risks.
  • Immunosuppressive drugs and biological agents used in treatment further increase susceptibility to infections.
  • Effective and safe vaccination is critical for managing these vulnerable patients.

Purpose of the Study:

  • To review current vaccination practices for pediatric rheumatic diseases.
  • To provide recommendations for future vaccination applications in this population.
  • To address the complexities of vaccine immunogenicity and safety in immunocompromised children.

Main Methods:

  • Literature review of current vaccination guidelines and research.
  • Analysis of vaccine immunogenicity in pediatric rheumatic disease patients compared to healthy individuals.
  • Evaluation of the safety of different vaccine types (live attenuated vs. inactivated) in relation to immunosuppressive therapies.

Main Results:

  • Live attenuated vaccines are generally contraindicated in patients receiving high-dose immunosuppressive drugs.
  • Inactivated vaccines are typically safe for patients with rheumatic diseases.
  • The immunomodulatory effects of biologic agents necessitate careful timing of live virus vaccinations post-treatment.

Conclusions:

  • Vaccination is essential but requires tailored strategies in pediatric rheumatic diseases.
  • Careful consideration of the patient's disease status and immunosuppressive therapy is crucial for vaccine selection and timing.
  • Future applications should focus on optimizing vaccine efficacy and safety in this high-risk group.

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