Persistence of MERS-CoV-spike-specific B cells and antibodies after late third immunization with the MVA-MERS-S vaccine

MVA-MERS-S疫苗第三次免疫接种后MERS-CoV刺突蛋白特异性B细胞和抗体的持久性

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作者:Leonie M Weskamm,Anahita Fathi,Matthijs P Raadsen,Anna Z Mykytyn,Till Koch,Michael Spohn,Monika Friedrich  ; MVA-MERS-S Study Group; Bart L Haagmans,Stephan Becker,Gerd Sutter,Christine Dahlke,Marylyn M Addo

Abstract

The Middle East respiratory syndrome (MERS) is a respiratory disease caused by MERS coronavirus (MERS-CoV). In follow up to a phase 1 trial, we perform a longitudinal analysis of immune responses following immunization with the modified vaccinia virus Ankara (MVA)-based vaccine MVA-MERS-S encoding the MERS-CoV-spike protein. Three homologous immunizations were administered on days 0 and 28 with a late booster vaccination at 12 ± 4 months. Antibody isotypes, subclasses, and neutralization capacity as well as T and B cell responses were monitored over a period of 3 years using standard and bead-based enzyme-linked immunosorbent assay (ELISA), 50% plaque-reduction neutralization test (PRNT50), enzyme-linked immunospot (ELISpot), and flow cytometry. The late booster immunization significantly increases the frequency and persistence of spike-specific B cells, binding immunoglobulin G1 (IgG1) and neutralizing antibodies but not T cell responses. Our data highlight the potential of a late boost to enhance long-term antibody and B cell immunity against MERS-CoV. Our findings on the MVA-MERS-S vaccine may be of relevance for coronavirus 2019 (COVID-19) vaccination strategies. Trial registration: ClinicalTrials.gov NCT03615911.

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