CYTOTOXIC T-LYMPHOCYTES SPECIFIC FOR HIV-1 GP160 ANTIGEN AND SYNTHETIC P18III(B) PEPTIDE IN AN HLA-A11-IMMUNIZED INDIVIDUAL

被引:25
作者
ACHOUR, A
LEMHAMMEDI, S
PICARD, O
MBIKA, JP
ZAGURY, JF
MOUKRIM, Z
WILLER, A
BEIX, F
BURNY, A
ZAGURY, D
机构
[1] HOP ST ANTOINE,PARIS,FRANCE
[2] UNIV LIBRE BRUXELLES,BRUSSELS,BELGIUM
关键词
D O I
10.1089/aid.1994.10.19
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Cytotoxic T cell determinants should be an important component of an anti-human immunodeficiency virus (HIV) vaccine. The epitopes of proteins can be defined with short synthetic peptides for class I-restricted CTLs. An immunodominant CTL epitope from the HIV-1 IIIB envelope protein gp160 comprising 15 amino acids (residues 315-329: RIQRGPGRAFVTIGK) (P18III(B)) has been identified that is recognized by class I MHC molecule H-2(d)-restricted murine CD8(+) CTLs. We have investigated the epitope specificity of anti-HIV-1 CTLs in immunized individuals and we found that the CTL response was restricted by more than one class I MHC molecule, including HLA-A2 and HLA-A3. In the present work, we also show that the response against P18III(B) peptide is restricted by the HLA-A11 molecule in an individual immunized by vaccinia virus expressing gp160 protein. This peptide could thus be recognized in association with different HLA class I allotypes. This work has implications for vaccine strategies, using the P18 peptide.
引用
收藏
页码:19 / 25
页数:7
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