Serostatus following live attenuated vaccination administered before pediatric liver transplantation

Takanori Funaki1, Kensuke Shoji1, Ippei Miyata1

  • 1Division of Infectious Diseases, Department of Medical Subspecialties, Center for Transplant Surgery, National Center for Child Health and Development, Tokyo, Japan.

Insights

Live attenuated vaccines (LAVs) before liver transplantation (LT) show high rubella immunogenicity but low rates for measles, varicella, and mumps. Further vaccination strategies and serological follow-up are recommended for pediatric patients awaiting LT.

Area of Science:

  • Immunology
  • Pediatric Gastroenterology
  • Hepatology

Background:

  • Live attenuated vaccines (LAVs) are typically contraindicated post-liver transplantation (LT).
  • Current guidelines recommend LAVs before LT for children aged ≥6 months, but supporting evidence is limited.
  • Assessing the immunogenicity of LAVs in pediatric patients prior to LT is crucial for optimizing vaccination strategies.

Purpose of the Study:

  • To evaluate the immunogenicity of LAVs administered before liver transplantation (LT) in pediatric patients.
  • To identify factors associated with seronegativity following LAV administration in this cohort.
  • To inform future vaccination guidelines for children undergoing LT.

Main Methods:

  • Serum antibody titers were measured using hemagglutination inhibition and ELISA tests for measles, rubella, varicella, and mumps.
  • Clinical data and vaccination history were collected from medical records of 49 patients.
  • Univariate and multivariate analyses were performed to determine factors influencing serostatus.

Main Results:

  • Seropositivity rates varied significantly: 46.9% for measles, 89.4% for rubella, 67.5% for varicella, and 48.8% for mumps.
  • Factors associated with seronegativity included younger vaccination age (<12 months) for measles, lower body weight for varicella, and non-biliary atresia underlying diseases for mumps.
  • No serious adverse events were reported during the study period.

Conclusions:

  • The immunogenicity of LAVs before LT is robust for rubella but suboptimal for measles, varicella, and mumps.
  • Current pre-LT vaccination protocols may require enhancement, particularly for certain vaccines and patient subgroups.
  • Targeted serological follow-up is advisable for pediatric LT candidates with identified risk factors for vaccine non-response.