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T-cell Epitopes Identified by BALB/c Mice Immunized with Vaccinia Expressing HIV-1 Gag lie within immunodominant Regions Recognized by HIV-infected Indian Patients.

AbstractBACKGROUND:
Human immunodeficiency virus (HIV) antigens from transmitted strains of HIV would prove crucial in vaccine designing for prevention of HIV infection. Immune response generated by Vaccinia construct expressing the HIV-1 gag gene from transmitted Indian HIV-1 subtype C strain (Vgag) in BALB/c mice is reported in the present study along with the identification of epitopes responsible for induction of the immune response.
AIMS:
The aim of this study was to determine immune response generated by the constructs in a mouse model and to understand the epitope specificities of the response.
SETTINGS AND DESIGN:
This was an observational study carried out in BALB/c mice.
MATERIALS AND METHODS:
The immunogenecity of Vgag construct was evaluated in BALB/c mice after multiple immunizations. T-cell response was monitored by the interferon-γ ELISPOT assay using HIV-1 C Gag overlapping peptides and anti-P24 antibodies were estimated by ELISA.
STATISTICAL ANALYSIS USED:
Graphpad prism software was used for statistical analysis and for plotting graphs.
RESULTS:
IFN-γ-secreting T cells and antibodies were detected against HIV Gag in mice after immunization. Although after repeated immunizations, antibody-mediated immune response increased or remained sustained, the magnitude of IFN-γ-secreting T cell was found to be decreased over time. The Gag peptides recognized by mice were mainly confined to the P24 region and had a considerable overlap with earlier reported immunodominant regions recognized by HIV-infected Indian patients.
CONCLUSION:
Vaccinia construct with a gag gene from transmitted HIV-1 virus was found to be immunogenic. The Gag regions identified by mice could have important implications in terms of future HIV vaccine designing.
AuthorsAshwini V Shete, Madhuri R Thakar, Srikanth P Tripathy, Cg Raut, Sekhar Chakrabarti, Ramesh S Paranjape
JournalJournal of global infectious diseases (J Glob Infect Dis) Vol. 3 Issue 3 Pg. 246-53 (Jul 2011) ISSN: 0974-8245 [Electronic] India
PMID21887056 (Publication Type: Journal Article)

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