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Updated data on effective and safe immunizations with live-attenuated vaccines for children after living donor liver
Masayoshi Shinjoh1, Ken Hoshino2, Takao Takahashi1
1Department of Pediatrics, Keio University School of Medicine, 35 Shinanomachi, Shinjuku-ku, Tokyo 160-8582, Japan.
Insights
Live-attenuated vaccines are safe and effective for pediatric liver transplant recipients not severely immunosuppressed. Repeat immunizations may be needed, except for rubella, to maintain immunity against viral diseases.
Area of Science:
- Pediatric immunology
- Transplant medicine
- Vaccinology
Background:
- Children post-liver transplant face risks from vaccine-preventable diseases.
- Limited vaccination opportunities exist before transplantation due to unstable health.
- Post-transplant immunity may wane, necessitating revaccination.
Purpose of the Study:
- To evaluate the safety and efficacy of live-attenuated vaccines in pediatric liver transplant recipients.
- To assess seroconversion rates and adverse events following vaccination.
- To determine the need for booster doses in this population.
Main Methods:
- Administered four individual live-attenuated vaccines (measles, rubella, varicella, mumps) subcutaneously to pediatric post-living donor liver transplant (LDLT) recipients meeting specific immunity criteria.
- Collected written informed consent.
- Included previously reported data from 18 cases (70 immunizations) and expanded the cohort.
Main Results:
- 196 immunizations were given to 48 pediatric post-LDLT recipients.
- High seroconversion rates were observed for measles (100%), rubella (100%), varicella (70%), and mumps (75%).
- No significant adverse events were reported; mild breakthrough varicella and transient parotid swelling occurred. Antibody levels remained stable for rubella vaccine.
Conclusions:
- Selected live-attenuated vaccines are safe and effective in pediatric post-LDLT patients who are not severely immunosuppressed.
- Repeated immunizations are likely necessary for measles, varicella, and mumps to ensure sustained immunity.
- Rubella vaccination demonstrated durable antibody levels, suggesting less need for repeat dosing.
Background:
Although immunizations using live-attenuated vaccines are not recommended for children post-liver transplant due to their theoretical risks, they will inevitably encounter vaccine-preventable viral diseases upon returning to real-life situations. The window of opportunity for vaccination is usually limited prior to transplantation because these children often have unstable disease courses. Also, vaccine immunity does not always persist after transplantation.
Methods:
Beginning in 2002, subcutaneous immunizations with four individual live-attenuated vaccines (measles, rubella, varicella, and mumps) to pediatric patients following living donor liver transplantation (LDLT) were performed for those who fulfilled the clinical criteria, including humoral and cell-mediated immunity. Written informed consent was collected. We included the study on 70 immunizations for 18 cases that we reported in 2008 (Shinjoh et al., 2008).
Results:
A total of 196 immunizations were administered to 48 pediatric post-LDLT recipients. Of these, 144 were first immunizations and 52 were repeated immunizations following LDLT. The seroconversion rates at the first dose for measles (AIK-C), rubella (TO-336), varicella (Oka), and mumps (Hoshino) were 100% (36/36), 100% (35/35), 70% (23/33), and 75% (24/32), respectively. Antibody levels did not fall over time in patients immunized with rubella vaccine. Three mild cases of breakthrough varicella were observed. Two cases with transient parotid gland swelling were observed after mumps immunization. Two admissions because of fever at 2-3 weeks after the measles vaccine were reported but the patients had no symptoms of measles.
Conclusions:
Immunizations using selected live-attenuated vaccines were safe and effective for post-LDLT children who were not severely immunosuppressed. However, with the exception of rubella, repeated immunization may be necessary.
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