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Dichotomy between the humoral and cellular responses elicited by mRNA and adenoviral vector vaccines against SARS-CoV-2

BACKGROUND: Protection from severe disease and hospitalization by SARS-CoV-2 vaccination has been amply demonstrated by real-world data. However, the rapidly evolving pandemic raises new concerns. One pertains efficacy of adenoviral vector-based vaccines, particularly the single-dose Ad26.COV2.S, re...

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Detalles Bibliográficos
Autores principales: Ukey, Rahul, Bruiners, Natalie, Mishra, Hridesh, Mishra, Pankaj K., McCloskey, Deborah, Onyuka, Alberta, Chen, Fei, Pinter, Abraham, Weiskopf, Daniela, Sette, Alessandro, Roy, Jason, Gaur, Sunanda, Gennaro, Maria Laura
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8786593/
https://www.ncbi.nlm.nih.gov/pubmed/35073931
http://dx.doi.org/10.1186/s12916-022-02252-0
Descripción
Sumario:BACKGROUND: Protection from severe disease and hospitalization by SARS-CoV-2 vaccination has been amply demonstrated by real-world data. However, the rapidly evolving pandemic raises new concerns. One pertains efficacy of adenoviral vector-based vaccines, particularly the single-dose Ad26.COV2.S, relative to mRNA vaccines. MAIN BODY: We investigated the immunogenicity of Ad26.COV2.S and mRNA vaccines in 33 subjects vaccinated with either vaccine class 5 months earlier on average. After controlling for the time since vaccination, Spike-binding antibody and neutralizing antibody levels were higher in the mRNA-vaccinated subjects, while no significant differences in antigen-specific B cell and T cell responses were observed between the two groups. CONCLUSIONS: A dichotomy exists between the humoral and cellular responses elicited by the two vaccine classes. Testing only for humoral responses to compare the durability of SARS-CoV-2 vaccine-induced responses, as typically performed for public health and research purposes, is insufficient. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12916-022-02252-0.