Viruses (Dec 2024)

Immune Response to SARS-CoV-2 XBB.1.5 and JN.1 Variants Following XBB.1.5 Booster Vaccination in Liver Transplant Recipients

  • Philippa von der Schulenburg,
  • Georg M. N. Behrens,
  • Markus Hoffmann,
  • Alexandra Linke,
  • Inga Nehlmeier,
  • Amy Madeleine Kempf,
  • Metodi Stankov,
  • Marc Lütgehetmann,
  • Jacqueline Jahnke-Triankowski,
  • Marylyn M. Addo,
  • Lutz Fischer,
  • Ansgar W. Lohse,
  • Stefan Pöhlmann,
  • Julian Schulze zur Wiesch,
  • Martina Sterneck

DOI
https://doi.org/10.3390/v16121942
Journal volume & issue
Vol. 16, no. 12
p. 1942

Abstract

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Background/Objectives: The efficacy of monovalent BNT162b2 Omicron XBB.1.5 booster vaccination in liver transplant recipients (LTRs) has yet to be described, particularly regarding the immune response to emerging variants like JN.1. Methods: This study evaluated humoral and cellular immune responses in 34 liver transplant recipients (LTRs) with varying SARS-CoV-2 immune histories before and after receiving a BNT162b2 Omicron XBB.1.5 booster vaccination. The assessment involved variant-specific serology, pseudovirus neutralization tests, and Interferon-γ release assays. Results: Participants had a median of four prior vaccinations, with 91.2% having a history of infection. Post-vaccination, significant increases in both Wuhan anti-S and Omicron-specific IgG antibodies and improved neutralization of B.1, XBB.1.5, and JN.1 pseudovirus particles were observed. Also, T-cell responses significantly increased post-vaccination. However, 17.6% of LTRs had no neutralizing antibodies against XBB.1.5 and JN.1, while 100% of healthy controls did. Shortly after vaccination, 18% of patients developed mild COVID-19. These LTRs had particularly low immune responses at baseline. Conclusions: The monovalent XBB.1.5 booster improved overall SARS-CoV-2-specific immunity. However, some LTRs still showed low or undetectable immune responses, indicating that ongoing monitoring and further booster doses are necessary in this high-risk group.

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