Real-world challenges in eligibility for MMR vaccination two years after autologous and allogeneic HSCT
Gopika Punchhi1, Rainbow Negus1, Hammad Saif1
1Schulich School of Medicine and Dentistry, Western University, London, ON, Canada.
Abstract:
Measles outbreaks have raised concerns of fatal infections in immunocompromised patients. Canadian guidelines advise administration of live vaccines, such as measles, mumps, and rubella (MMR), two yearsafter hematopoietic stem cell transplant (HSCT) yet studies have not assessed eligibility based on medication contraindications. We retrospectively reviewed the charts of 72 autologous (auto-HSCT) and 68 allogeneic (allo-HSCT) recipients at the Windsor Regional Cancer Center to determine MMR reactivity and eligibility based on administration of contraindicated medications two years post-HSCT. Reactivity to measles, mumps, and rubella in auto-HSCT recipients was 49.1 %, 28.8 %, and 52.3 %, respectively, and in allo-HSCT recipients was 75.6 %, 57.8 %, and 64.4 %, respectively. Immunity to all three components was significantly different between transplant types (p = 0.0002). Nearly 80 % of auto-HSCT patients were on a contraindicated medication at two years compared to 45 % of allo-HSCT recipients. Auto-HSCT recipients require MMR revaccination, but it is contraindicated in a large proportion of patients.
Insights
Measles, mumps, and rubella (MMR) revaccination is recommended post-hematopoietic stem cell transplant (HSCT). However, many autologous HSCT patients cannot receive MMR due to contraindicated medications two years after transplant.
Area of Science:
- Immunology
- Transplantation Medicine
- Infectious Disease Epidemiology
Background:
- Measles outbreaks pose risks to immunocompromised individuals, particularly post-hematopoietic stem cell transplant (HSCT).
- Current Canadian guidelines recommend measles, mumps, and rubella (MMR) vaccination two years after HSCT.
- Eligibility for MMR vaccination post-HSCT has not been fully assessed considering medication contraindications.
Purpose of the Study:
- To evaluate MMR vaccine immunity and eligibility in autologous (auto-HSCT) and allogeneic (allo-HSCT) recipients.
- To determine the proportion of HSCT recipients on medications that contraindicate MMR vaccination two years post-transplant.
Main Methods:
- Retrospective chart review of 72 auto-HSCT and 68 allo-HSCT recipients.
- Assessment of MMR seroreactivity.
- Identification of patients on contraindicated medications at two years post-HSCT.
Main Results:
- Lower MMR immunity observed in auto-HSCT recipients (49.1% measles, 28.8% mumps, 52.3% rubella) compared to allo-HSCT recipients (75.6% measles, 57.8% mumps, 64.4% rubella).
- Significant differences in immunity to all three MMR components between auto-HSCT and allo-HSCT groups (p=0.0002).
- Nearly 80% of auto-HSCT patients and 45% of allo-HSCT patients were on contraindicated medications two years post-transplant.
Conclusions:
- Autologous HSCT recipients exhibit lower MMR immunity and a higher rate of medication contraindications for MMR vaccination.
- Current guidelines for MMR vaccination post-HSCT may not be suitable for all patients, especially auto-HSCT recipients.
- Further strategies are needed to ensure measles protection in immunocompromised patients post-HSCT who cannot receive live vaccines.
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