Identification of cryptic MHC I-restricted epitopes encoded by HIV-1 alternative reading frames

被引:71
作者
Cardinaud, S
Moris, A
Février, M
Rohrlich, PS
Weiss, L
Langlade-Demoyen, P
Lemonnier, FA
Schwartz, O
Habel, A
机构
[1] Inst Pasteur, Unite Cellulaire Antivirale, CNRS, Unite Associe Rech 1930, F-75724 Paris 15, France
[2] Hop Europeen Georges Pompidou, Serv Immunol Clin, F-75908 Paris 15, France
关键词
HLA-B7; CTL; transgenic mice; KO mice;
D O I
10.1084/jem.20031869
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Human immunodeficiency virus (HIV) 1 major histocompatibility complex (MHC) I-restricted epitopes are widely believed to be derived from viral proteins encoded by primary open reading frames. However, the HIV-1 genome contains alternative reading frames (ARFs) potentially encoding small polypeptides. We have identified a panel of epitopes encoded by ARFs within the gag, pol, and env genes. The corresponding epitopic peptides were immunogenic in mice humanized for MHC-I molecules. In addition, cytotoxic T lymphocytes recognizing these epitopes were found in HIV-infected patients. These results reveal the existence of atypical mechanisms of HIV-1 epitope generation. They indicate that the repertoire of epitopes recognized by the cellular anti-HIV-1 immune response is broader than initially thought. This should be taken Into account when designing vaccine strategies aimed at activating these responses.
引用
收藏
页码:1053 / 1063
页数:11
相关论文
共 44 条
[31]   Frameshift-mutation-derived peptides as tumor-specific antigens in inherited and spontaneous colorectal cancer [J].
Saeterdal, I ;
Bjorheim, J ;
Lislerud, K ;
Gjertsen, MK ;
Bukholm, IK ;
Olsen, OC ;
Nesland, JM ;
Eriksen, JA ;
Moller, M ;
Lindblom, A ;
Gaudernack, G .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (23) :13255-13260
[32]   +1 frameshifting as a novel mechanism to generate a cryptic cytotoxic T lymphocyte epitope derived from human interleukin 10 [J].
Saulquin, X ;
Scotet, E ;
Trautmann, L ;
Peyrat, MA ;
Halary, F ;
Bonneville, M ;
Houssaint, E .
JOURNAL OF EXPERIMENTAL MEDICINE, 2002, 195 (03) :353-358
[33]   Control of viremia in simian immunodeficiency virus infection by CD8+ lymphocytes [J].
Schmitz, JE ;
Kuroda, MJ ;
Santra, S ;
Sasseville, VG ;
Simon, MA ;
Lifton, MA ;
Racz, P ;
Tenner-Racz, K ;
Dalesandro, M ;
Scallon, BJ ;
Ghrayeb, J ;
Forman, MA ;
Montefiori, DC ;
Rieber, EP ;
Letvin, NL ;
Reimann, KA .
SCIENCE, 1999, 283 (5403) :857-860
[34]   Rapid degradation of a large fraction of newly synthesized proteins by proteasomes [J].
Schubert, U ;
Antón, LC ;
Gibbs, J ;
Norbury, CC ;
Yewdell, JW ;
Bennink, JR .
NATURE, 2000, 404 (6779) :770-774
[35]   Constitutive display of cryptic translation products by MHC class I molecules [J].
Schwab, SR ;
Li, KC ;
Kang, C ;
Shastri, N .
SCIENCE, 2003, 301 (5638) :1367-1371
[36]   HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 NEF INCREASES THE EFFICIENCY OF REVERSE TRANSCRIPTION IN THE INFECTED CELL [J].
SCHWARTZ, O ;
MARECHAL, V ;
DANOS, O ;
HEARD, JM .
JOURNAL OF VIROLOGY, 1995, 69 (07) :4053-4059
[37]   Producing nature's gene-chips: The generation of peptides for display by MHC class I molecules [J].
Shastri, N ;
Schwab, S ;
Serwold, T .
ANNUAL REVIEW OF IMMUNOLOGY, 2002, 20 :463-493
[38]  
Smith KD, 1996, J IMMUNOL, V156, P3755
[39]   NUCLEOTIDE-SEQUENCE OF THE AIDS VIRUS, LAV [J].
WAINHOBSON, S ;
SONIGO, P ;
DANOS, O ;
COLE, S ;
ALIZON, M .
CELL, 1985, 40 (01) :9-17
[40]   Utilization of an alternative open reading frame of a normal gene in generating a novel human cancer antigen [J].
Wang, RF ;
Parkhurst, MR ;
Kawakami, Y ;
Robbins, PF ;
Rosenberg, SA .
JOURNAL OF EXPERIMENTAL MEDICINE, 1996, 183 (03) :1131-1140