Novel Modified Vaccinia Virus Ankara Vector Expressing Anti-apoptotic Gene B13R Delays Apoptosis and Enhances Humoral Responses

Author:

Chea Lynette S.12,Wyatt Linda S.3,Gangadhara Sailaja12,Moss Bernard3ORCID,Amara Rama R.12

Affiliation:

1. Department of Microbiology and Immunology, Emory University School of Medicine, Atlanta, Georgia, USA

2. Division of Microbiology and Immunology, Emory Vaccine Center, Yerkes National Primate Research Center, Emory University, Atlanta, Georgia, USA

3. Laboratory of Viral Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland, USA

Abstract

MVA is an attractive viral vector for vaccine development due to its safety and immunogenicity in multiple species and humans even under conditions of immunodeficiency. Here, to further improve the immunogenicity of MVA, we developed a novel vector, MVA- B13R , by replacing the fragmented anti-apoptotic genes 181R / 182R with a functional version derived from vaccinia virus, B13R . Our results show that MVA- B13R significantly delays apoptosis in antigen-presenting cells and muscle cells in vitro and augments vaccine-induced humoral immunity in mice, leading to the development of a novel vector for vaccine development against infectious diseases and cancer.

Funder

HHS | National Institutes of Health

HHS | NIH | National Center for Research Resources

Emory University | Center for AIDS Research, Emory University

Publisher

American Society for Microbiology

Subject

Virology,Insect Science,Immunology,Microbiology

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