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Published on: May 7, 2012
Effective and safe immunizations with live-attenuated vaccines for children after living donor liver transplantation
Masayoshi Shinjoh1, Isao Miyairi, Ken Hoshino
1Department of Pediatrics, School of Medicine, Keio University, Shinjuku-ku, Tokyo 160-8582, Japan. m.shinjo@z2.keio.jp
Insights
Live-attenuated vaccines are safe and effective for pediatric liver transplant recipients. Immunizations with measles, rubella, varicella, and mumps vaccines showed high seroconversion rates without serious adverse events.
Area of Science:
- Pediatric Gastroenterology and Hepatology
- Immunology
- Transplant Medicine
Background:
- Live-attenuated vaccines are generally contraindicated in pediatric liver transplant (LT) recipients due to theoretical risks.
- Post-LT children face exposure to vaccine-preventable viral diseases in community settings.
- Assessing the safety and efficacy of live-attenuated vaccines is crucial for this vulnerable population.
Purpose of the Study:
- To evaluate the safety and immunogenicity of live-attenuated vaccines in pediatric living donor liver transplant (LDLT) recipients.
- To determine seroconversion rates and assess adverse events following vaccination.
- To investigate the durability of immune response after vaccination.
Main Methods:
- Seventy immunizations with four live-attenuated vaccines (measles, rubella, varicella, mumps) were administered to 18 pediatric LDLT recipients meeting specific immunity criteria.
- Seroconversion rates were assessed after the first vaccine dose.
- Patients were monitored for clinical diseases and serious adverse effects for up to 5 years and 11 months.
Main Results:
- High seroconversion rates were observed: 100% for measles and rubella, and 82% for varicella and mumps.
- Waning immunity was noted in some cases, except after rubella immunization.
- No clinical diseases or serious adverse effects related to the immunizations were reported.
Conclusions:
- Selected live-attenuated vaccines are safe and effective in pediatric LDLT recipients with adequate humoral and cell-mediated immunity.
- Vaccination strategies should be considered for post-LT children to prevent vaccine-preventable diseases.
- Careful patient selection and monitoring are essential for successful live-attenuated vaccine administration in this cohort.
Abstract:
Immunizations using live-attenuated vaccines are not recommended for post-liver transplant children due to its theoretical risks. However, they will encounter vaccine-preventable viral diseases upon returning to real-life situations. We performed a total of 70 immunizations with four individual live-attenuated vaccines to 18 pediatric post-living donor liver transplant (LDLT) recipients who fulfilled a clinical criteria including humoral and cell-mediated immunity. The seroconversion rates at the first dose for measles (strain AIK-C), rubella (strain TO-336), varicella (strain Oka), and mumps (strains Hoshino) were 100% (15/15), 100% (15/15), 82% (9/11), and 82% (9/11), respectively. During observed period (-5 years 11 months), a few cases with waning immunity (antibodies were once produced but the levels fell over time) were seen except after rubella immunization. Clinical diseases after seroconversion or definite serious adverse effects due to immunization were not observed. Immunizations using selected live-attenuated vaccines were safe and effective for post-LDLT children who were not severely immunosuppressed.
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