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.
|
Authors | Wei Liu, Yan Zhou, Ziyan Wang, Zeqiang Zhang, Qizhi Wang, Weiheng Su, Yan Chen, Yan Zhang, Feng Gao, Chunlai Jiang, Wei Kong |
Journal | Microbiology and immunology
(Microbiol Immunol)
Vol. 61
Issue 5
Pg. 176-184
(May 2017)
ISSN: 1348-0421 [Electronic] Australia |
PMID | 28378925
(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)
|