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Evaluation of recombinant adenovirus vaccines based on glycoprotein D and truncated UL25 against herpes simplex virus type 2 in mice.

Abstract
The high prevalence of herpes simplex virus 2 (HSV-2) infections in humans necessitates the development of a safe and effective vaccine that will need to induce vigorous T-cell responses to control viral infection and transmission. We designed rAd-gD2, rAd-gD2ΔUL25, and rAd-ΔUL25 to investigate whether recombinant replication-defective adenoviruses vaccine could induce specific T-cell responses and protect mice against intravaginal HSV-2 challenge compared with FI-HSV-2. In the present study, recombinant adenovirus-based HSV-2 showed higher reductions in mortality and stronger antigen-specific T-cell responses compared with FI-HSV-2 and the severity of genital lesions in mice immunized with rAd-gD2ΔUL25 was significantly decreased by eliciting IFN-γ-secreting T-cell responses compared with rAd-gD2 and rAd-ΔUL25 groups. Our results demonstrated the immunogenicity and protective efficacy of recombinant adenovirus vaccines in acute HSV-2 infection following intravaginal challenge in mice.
AuthorsWei Liu, Yan Zhou, Ziyan Wang, Zeqiang Zhang, Qizhi Wang, Weiheng Su, Yan Chen, Yan Zhang, Feng Gao, Chunlai Jiang, Wei Kong
JournalMicrobiology and immunology (Microbiol Immunol) Vol. 61 Issue 5 Pg. 176-184 (May 2017) ISSN: 1348-0421 [Electronic] Australia
PMID28378925 (Publication Type: Journal Article)
Copyright© 2017 The Societies and John Wiley & Sons Australia, Ltd.
Chemical References
  • Adenovirus Vaccines
  • Capsid Proteins
  • Glycoproteins
  • IFNG protein, mouse
  • UL25 protein, herpes simplex virus type 2
  • Vaccines, Synthetic
  • Viral Envelope Proteins
  • Interferon-gamma
Topics
  • Adenoviridae (immunology)
  • Adenovirus Vaccines (immunology)
  • Administration, Intravaginal
  • Animals
  • Capsid Proteins (genetics, immunology)
  • Disease Models, Animal
  • Female
  • Glycoproteins (immunology)
  • Herpes Genitalis (immunology, prevention & control, virology)
  • Herpesvirus 2, Human (immunology)
  • Interferon-gamma (immunology)
  • Mice
  • Mice, Inbred BALB C
  • Vaccines, Synthetic (immunology)
  • Viral Envelope Proteins (immunology)

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