| Literature DB >> 11152503 |
M A Altfeld1, B Livingston, N Reshamwala, P T Nguyen, M M Addo, A Shea, M Newman, J Fikes, J Sidney, P Wentworth, R Chesnut, R L Eldridge, E S Rosenberg, G K Robbins, C Brander, P E Sax, S Boswell, T Flynn, S Buchbinder, P J Goulder, B D Walker, A Sette, S A Kalams.
Abstract
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.Entities:
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Year: 2001 PMID: 11152503 PMCID: PMC114036 DOI: 10.1128/JVI.75.3.1301-1311.2001
Source DB: PubMed Journal: J Virol ISSN: 0022-538X Impact factor: 5.103