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

Publication date: Dec 19, 2024

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. 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. 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. 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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Concepts Keywords
Bnt162b2 Adult
Healthy Aged
Transplant Antibodies, Neutralizing
Vaccination Antibodies, Neutralizing
Viruses Antibodies, Viral
Antibodies, Viral
BNT162 Vaccine
BNT162 Vaccine
cellular immune response
COVID-19
COVID-19
COVID-19 Vaccines
COVID-19 Vaccines
Female
Humans
humoral immune response
Immunity, Cellular
Immunity, Humoral
Immunization, Secondary
Immunoglobulin G
Immunoglobulin G
immunosuppression
JN.1
Liver Transplantation
liver transplantation
Male
Middle Aged
SARS-CoV-2
SARS-CoV-2
Transplant Recipients
Vaccination
vaccination
XBB.1.5

Semantics

Type Source Name
disease IDO immune response
pathway REACTOME Release
disease IDO history
disease MESH infection
disease IDO cell
disease MESH COVID-19
drug DRUGBANK Coenzyme M
disease IDO immunosuppression
disease IDO protein
disease IDO blood
disease IDO assay
disease IDO production
disease MESH hypertension
disease MESH comorbidity
disease MESH breakthrough infection
drug DRUGBANK Cysteamine
disease IDO humoral immune response

Original Article

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