10.22376/ijpbs.2019.10.1.p1-12 Volume 5 Issue 4 2014 (October - December) Human immunodeficiency virus (HIV) a retrovirus that belongs to the Lentiviridae family, is the causative agent for Acquired Immuno Deficiency Syndrome. Certain "protective" HLA alleles play significant role low viraemia condition like HLA-DRB1*15 allele. An Insilco analysis was adopted to identify Gag epitopes vaccine candidates namely P1-P6 (GLNKIVRMYSPTSIL, LGLNKIVRMYSPTSI, LNKIVRMYSPTSILD, NKIVRMYSPTSILDI, IVRMYSPTSILDIKQ, KIVRMYSPTSILDI) restricted to HLA-DRB1*15 allele would aid significant CD4+ T cell immune response against HIV infection and population coverage among Indian population assessed. Three dimensional structure of epitopes P1-P6 modeled using PEPFOLD, and were tested for their binding affinity towards HLA binding groove using GRAMMX based docking studies resulted with conventional hydrogen bonding,pi-donor,pi-sulfur,carbon hydrogen bonding ,pi-alkyl interaction. Thus the interaction between the screened P1-P6 epitopes exhibiting stability would aid immune response. This computational study of a Gag epitope-based peptide vaccine design for HIV would be helpful in determining novel pep­tide antigen targets in GAG proteins which need to be validated in vitro and in vivo experiments. JEMMY CHRISTY.H AND ALEX ANAND.D HIV Vaccine, HLA-DRB1*15, Gag epitope, CD4+ T cell response, HLA-Epitope,Affinity. 1212-1222