Publication date: Jul 20, 2024
A monovalent Omicron XBB.1.5 mRNA RBD analogue vaccine, MAFB-7256a (DS-5670d), was newly developed and approved in Japan in the Spring of 2024 for preventing COVID-19. However, clinical efficacy data for this vaccine are currently lacking. We previously established the Quantification of Antigen-specific Antibody Sequence (QASAS) method to assess the response to SARS-CoV-2 vaccination at the mRNA level using B-cell receptor (BCR) repertoire assays and the Coronavirus Antibody Database (CoV-AbDab). Here, we used this method to evaluate the immunogenicity of MAFB-7256a. We analyzed repeated blood samples using the QASAS method from three healthy volunteers before and after MAFB-7256a vaccination. BCR response increased rapidly one week post-vaccination and then decreased, as with conventional vaccine. Notably, the matched sequences after MAFB-7256a vaccination specifically bound to the receptor-binding domain (RBD), with no sequences binding to other epitopes. These results validate that MAFB-7256a is an effective vaccine that exclusively induces antibodies specific for the RBD, demonstrating its targeted immunogenic effect.
Concepts | Keywords |
---|---|
Bioinformatics | 7256a |
Coronavirus | Antibody |
Silkworm | Cdr3 |
Unbiased | Cov |
Distance | |
Mafb | |
Matched | |
Medrxiv | |
Mrna | |
Preprint | |
Rbd | |
Sars | |
Sequences | |
Vaccination | |
Vaccine |
Semantics
Type | Source | Name |
---|---|---|
disease | IDO | cell |
disease | VO | vaccine |
disease | MESH | COVID-19 |
disease | VO | vaccination |
disease | IDO | blood |
disease | VO | effective |
disease | MESH | Infection |
disease | MESH | Infectious Diseases |
drug | DRUGBANK | Amino acids |
disease | IDO | host |
drug | DRUGBANK | Angiotensin II |
disease | IDO | history |
disease | VO | protocol |
disease | VO | USA |
disease | VO | manufacturer |
disease | VO | titer |
disease | VO | Viruses |
disease | VO | vaccinated |
disease | IDO | immune response |
disease | VO | effectiveness |
disease | VO | immunization |
disease | VO | efficient |
disease | MESH | malignancy |
disease | IDO | site |