Longitudinal analysis of B- and T-cell responses to SARS-CoV-2 recombinant S-protein vaccine S-268019-b in phase 1/2 priming and booster study

Publication date: Oct 02, 2024

The durability of vaccine-induced immune memory to severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is crucial for preventing infection, especially severe disease. This follow-up report from a phase 1/2 study of S-268019-b (a recombinant spike protein vaccine) after homologous booster vaccination confirms its long-term safety, tolerability, and immunogenicity. Booster vaccination with S-268019-b resulted in an enhancement of serum neutralizing antibody (NAb) titers and a broad range of viral neutralization. Single-cell immune profiling revealed persistent and mature antigen-specific memory B cells and T follicular helper cells, with increased B-cell receptor diversity. The expansion of B- and T-cell repertoires and presence of cross-reactive NAbs targeting conserved epitopes within the receptor-binding domain following a booster accounted for the broad-spectrum neutralizing activity. These findings highlight the potential of S-268019-b to provide broad and robust protection against a range of SARS-CoV-2 variants, addressing a critical challenge in the ongoing fight against coronavirus disease 2019 (COVID-19).

PDF

Concepts Keywords
Biotechnologies Bmem
Jp21nf0101626 Booster
June Clones
Vaccine Cov
Day
Epitopes
Figure
Medrxiv
Preprint
Sars
Supplementary
Vaccination
Vaccine

Semantics

Type Source Name
disease IDO cell
disease MESH infection
disease IDO protein
disease MESH coronavirus disease 2019
drug DRUGBANK Squalene
drug DRUGBANK Water
disease IDO production
disease IDO blood
disease IDO disposition
disease IDO intervention
drug DRUGBANK Ethanol
disease MESH erythema
disease MESH vertigo
disease MESH hypertension
disease MESH shock
disease IDO assay
drug DRUGBANK Tretamine
drug DRUGBANK Tocopherol
pathway REACTOME Immune System

Download Document

(Visited 2 times, 1 visits today)