Comparative analysis of the impact of 40 adenovirus types on dendritic cell activation and CD8+ T cell proliferation capacity for the identification of favorable immunization vector candidates

Front Immunol. 2023 Oct 17:14:1286622. doi: 10.3389/fimmu.2023.1286622. eCollection 2023.

Abstract

For the development of new adenovirus (AdV)-based vectors, it is important to understand differences in immunogenicity. In a side-by-side in vitro analysis, we evaluated the effect of 40 AdV types covering human AdV (HAdV) species A through G on the expression of 11 activation markers and the secretion of 12 cytokines by AdV-transduced dendritic cells, and the effect on CD8+ T cell proliferation capacity. We found that the expression of activation markers and cytokines differed widely between the different HAdV types, and many types were able to significantly impair the proliferation capacity of CD8+ T cells. Univariate and multivariate regression analyses suggested an important role of type I interferons in mediating this suppression of CD8+ T cells, which we confirmed experimentally in a proliferation assay using a type I interferon receptor blocking antibody. Using Bayesian statistics, we calculated a prediction model that suggests HAdV types HAdV-C1, -D8, -B7, -F41, -D33, -C2, -A31, -B3 and -D65 as the most favorable candidates for vaccine vector development.

Keywords: CD8 T cell response; CD8+ T cell response; T cell response; adenoviral vector; adenovirus-based immunization; human adenovirus (HAdV); immunogenicity.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenoviridae* / genetics
  • Adenoviruses, Human
  • Bayes Theorem
  • CD8-Positive T-Lymphocytes*
  • Cell Proliferation
  • Cytokines
  • Dendritic Cells
  • Humans
  • Immunization

Substances

  • Cytokines

Supplementary concepts

  • Human mastadenovirus A

Grants and funding

The author(s) declare financial support was received for the research, authorship, and/or publication of this article. This work was supported by a stipend from the China Scholarship Council to XW and by a grant from the Deutsche Forschungsgemeinschaft to WB (BA 4432/1-4). We acknowledge support from the Open Access Publication Fund of the University of Duisburg-Essen.