Reevaluating immunization delays after red blood cell transfusion

Alexandra Zabeida1,2, Marc H Lebel3,4, Christian Renaud3,4

  • 1Department of Pediatrics, Montreal Children's Hospital, Montreal, Quebec, Canada.

Transfusion
|July 5, 2019
PubMed

Insights

Children receiving frequent blood transfusions can be safely immunized with the measles, mumps, and rubella (MMR) vaccine. This study found high vaccine immunogenicity, suggesting current immunization delay guidelines may be unnecessary.

Area of Science:

  • Pediatrics
  • Immunology
  • Hematology

Background:

  • Current guidelines recommend delaying live vaccines like MMR by 5-6 months post-RBC transfusion.
  • These recommendations, based on limited data, may hinder timely vaccination for children needing frequent transfusions.
  • This study investigates MMR vaccine immunogenicity in chronically transfused pediatric patients.

Purpose of the Study:

  • To assess measles, mumps, rubella (MMR) vaccine immunogenicity in pediatric patients receiving chronic red blood cell (RBC) transfusions.
  • To quantify MMR vaccine antibodies present in RBC donations.

Main Methods:

  • Quantified MMR-specific antibodies in 25 pediatric patients post-vaccination while on chronic RBC transfusion.
  • Analyzed MMR antibodies in supernatants from 30 RBC donations.
  • Compared antibody levels with vaccination dates and blood donor birth years.

Main Results:

  • Measles, mumps, and rubella vaccine immunity ranged from 68% to 76% in transfused patients.
  • Pre-1976 blood donors (pre-MMR vaccine era) showed higher MMR antibody levels (67%) in donations compared to post-1976 donors (7%).
  • MMR antibody levels in RBC donations appear to decrease over time.

Conclusions:

  • This is the first study demonstrating MMR vaccine immunogenicity in chronically transfused patients.
  • Despite lower rates than general populations, MMR vaccine immunogenicity is significant in this cohort.
  • Re-evaluation of current immunization delay guidelines after RBC transfusions is warranted to optimize disease prevention in vulnerable children.
Abstract

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