Bovine Adenoviral Vector-Based Platform for Vaccine Development

Adenoviral (AdV) vector-based vaccines employing the human AdV (HAdV) and chimpanzee AdV (ChAdV) vector platforms played a crucial role in combating the COVID-19 pandemic. However, the widespread use of these platforms, the prevalence of various HAdV types, and the resulting preexisting immunity hav...

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Main Authors: Ekramy E. Sayedahmed, Vivek Gairola, Muralimanohara S. T. Murala, Suresh K. Mittal
Format: Article
Language:English
Published: MDPI AG 2025-05-01
Series:Vaccines
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Online Access:https://www.mdpi.com/2076-393X/13/5/494
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author Ekramy E. Sayedahmed
Vivek Gairola
Muralimanohara S. T. Murala
Suresh K. Mittal
author_facet Ekramy E. Sayedahmed
Vivek Gairola
Muralimanohara S. T. Murala
Suresh K. Mittal
author_sort Ekramy E. Sayedahmed
collection DOAJ
description Adenoviral (AdV) vector-based vaccines employing the human AdV (HAdV) and chimpanzee AdV (ChAdV) vector platforms played a crucial role in combating the COVID-19 pandemic. However, the widespread use of these platforms, the prevalence of various HAdV types, and the resulting preexisting immunity have significantly impacted the vaccines utilizing these vector platforms. Considering these challenges, the bovine AdV type 3 (BAdV-3) vector system has emerged as a versatile and innovative platform for developing next-generation vaccines against infectious diseases. Inherent attributes like a high transduction efficiency, large transgene insertion capacity, broad tissue tropism, and robust induction of innate immunity add significant value to the BAdV vector platform for vaccine design. BAdV-3 vectors effectively elude HAdV-specific preexisting humoral and cellular immune responses. Additionally, BAdV-3 is low in pathogenicity for its host and is anticipated to be safe as a vaccine platform. This systematic review provides an overview of the development of BAdV-3 as a vaccine delivery platform and its application in designing vaccines for infectious agents of human and veterinary importance.
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institution Kabale University
issn 2076-393X
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publishDate 2025-05-01
publisher MDPI AG
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series Vaccines
spelling doaj-art-69df10e3d1bc408ab7bbaeb4fdbdb4852025-08-20T03:48:01ZengMDPI AGVaccines2076-393X2025-05-0113549410.3390/vaccines13050494Bovine Adenoviral Vector-Based Platform for Vaccine DevelopmentEkramy E. Sayedahmed0Vivek Gairola1Muralimanohara S. T. Murala2Suresh K. Mittal3Department of Comparative Pathobiology and Purdue Institute of Inflammation, Immunology and Infectious Disease, College of Veterinary Medicine, Purdue University, 625 Harrison St., West Lafayette, IN 47907-2027, USADepartment of Comparative Pathobiology and Purdue Institute of Inflammation, Immunology and Infectious Disease, College of Veterinary Medicine, Purdue University, 625 Harrison St., West Lafayette, IN 47907-2027, USADepartment of Comparative Pathobiology and Purdue Institute of Inflammation, Immunology and Infectious Disease, College of Veterinary Medicine, Purdue University, 625 Harrison St., West Lafayette, IN 47907-2027, USADepartment of Comparative Pathobiology and Purdue Institute of Inflammation, Immunology and Infectious Disease, College of Veterinary Medicine, Purdue University, 625 Harrison St., West Lafayette, IN 47907-2027, USAAdenoviral (AdV) vector-based vaccines employing the human AdV (HAdV) and chimpanzee AdV (ChAdV) vector platforms played a crucial role in combating the COVID-19 pandemic. However, the widespread use of these platforms, the prevalence of various HAdV types, and the resulting preexisting immunity have significantly impacted the vaccines utilizing these vector platforms. Considering these challenges, the bovine AdV type 3 (BAdV-3) vector system has emerged as a versatile and innovative platform for developing next-generation vaccines against infectious diseases. Inherent attributes like a high transduction efficiency, large transgene insertion capacity, broad tissue tropism, and robust induction of innate immunity add significant value to the BAdV vector platform for vaccine design. BAdV-3 vectors effectively elude HAdV-specific preexisting humoral and cellular immune responses. Additionally, BAdV-3 is low in pathogenicity for its host and is anticipated to be safe as a vaccine platform. This systematic review provides an overview of the development of BAdV-3 as a vaccine delivery platform and its application in designing vaccines for infectious agents of human and veterinary importance.https://www.mdpi.com/2076-393X/13/5/494bovine adenoviruspathogenesisvirion structuregenome organizationbovine adenoviral vector-based platformnonhuman adenoviral vector system
spellingShingle Ekramy E. Sayedahmed
Vivek Gairola
Muralimanohara S. T. Murala
Suresh K. Mittal
Bovine Adenoviral Vector-Based Platform for Vaccine Development
Vaccines
bovine adenovirus
pathogenesis
virion structure
genome organization
bovine adenoviral vector-based platform
nonhuman adenoviral vector system
title Bovine Adenoviral Vector-Based Platform for Vaccine Development
title_full Bovine Adenoviral Vector-Based Platform for Vaccine Development
title_fullStr Bovine Adenoviral Vector-Based Platform for Vaccine Development
title_full_unstemmed Bovine Adenoviral Vector-Based Platform for Vaccine Development
title_short Bovine Adenoviral Vector-Based Platform for Vaccine Development
title_sort bovine adenoviral vector based platform for vaccine development
topic bovine adenovirus
pathogenesis
virion structure
genome organization
bovine adenoviral vector-based platform
nonhuman adenoviral vector system
url https://www.mdpi.com/2076-393X/13/5/494
work_keys_str_mv AT ekramyesayedahmed bovineadenoviralvectorbasedplatformforvaccinedevelopment
AT vivekgairola bovineadenoviralvectorbasedplatformforvaccinedevelopment
AT muralimanoharastmurala bovineadenoviralvectorbasedplatformforvaccinedevelopment
AT sureshkmittal bovineadenoviralvectorbasedplatformforvaccinedevelopment