Identification of novel HLA-A2-restricted human immunodeficiency virus type 1-specific cytotoxic T-lymphocyte epitopes predicted by the HLA-A2 supertype peptide-binding motif

被引:83
作者
Altfeld, MA
Livingston, B
Reshamwala, N
Nguyen, PT
Addo, MM
Shea, A
Newman, M
Fikes, J
Sidney, J
Wentworth, P
Chesnut, R
Eldridge, RL
Rosenberg, ES
Robbins, GK
Brander, C
Sax, PE
Boswell, S
Flynn, T
Buchbinder, S
Goulder, PJR
Walker, BD
Sette, A
Kalams, SA
机构
[1] Massachusetts Gen Hosp, Partners AIDS Res Ctr, Boston, MA 02114 USA
[2] Massachusetts Gen Hosp, Infect Dis Unit, Boston, MA 02114 USA
[3] Harvard Univ, Sch Med, Brigham & Womens Hosp, Dept Med, Boston, MA USA
[4] Fenway Community Hlth Ctr, Boston, MA USA
[5] Epimmune Inc, San Diego, CA USA
[6] Dept Publ Hlth, AIDS Off, San Francisco, CA USA
关键词
D O I
10.1128/JVI.75.3.1301-1311.2001
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Virus-specific cytotoxic T-lymphocyte (CTL) responses are critical in the control of human immunodeficiency virus type 1 (HIV-1) infection and will play an important part in therapeutic and prophylactic HIV-1 vaccines. The identification of virus specific epitopes that are efficiently recognized by CTL is the first step in the development of future vaccines. Here we describe the immunological characterization of a number of novel HIV-1-specific, HLA-A2-restricted CTL epitopes that share a high degree of conservation within HIV-1 and a strong binding to different alleles of the HLA-A2 superfamily. These novel epitopes include the first reported CTL epitope in the Vpr protein. Two of the novel epitopes were immunodominant among the HLA-A2-restricted CTL responses of individuals with acute and chronic HIV-1 infection. The novel CTL epitopes identified here should be included in future vaccines designed to induce HIV-1-specific CTL responses restricted by the HLA-A2 superfamily and will be important to assess in immunogenicity studies in infected persons and in uninfected recipients of candidate HIV-1 vaccines.
引用
收藏
页码:1301 / 1311
页数:11
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