Recognition of the highly conserved YMDD region in the human immunodeficiency virus type 1 reverse transcriptase by HLA-A2-restricted cytotoxic T lymphocytes from an asymptomatic long-term nonprogressor

被引:67
作者
Harrer, E
Harrer, T
Barbosa, P
Feinberg, M
Johnson, RP
Buchbinder, S
Walker, BD
机构
[1] MASSACHUSETTS GEN HOSP,AIDS RES CTR & INFECT DIS UNIT,BOSTON,MA 02114
[2] HARVARD UNIV,SCH MED,BOSTON,MA
[3] MASSACHUSETTS GEN HOSP,BOSTON,MA 02114
[4] UNIV CALIF SAN FRANCISCO,GLADSTONE INST,SAN FRANCISCO,CA
[5] UNIV CALIF SAN FRANCISCO,CTR AIDS RES,SAN FRANCISCO,CA
[6] DEPT PUBL HLTH,AIDS OFF,SAN FRANCISCO,CA
关键词
D O I
10.1093/infdis/173.2.476
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The human immunodeficiency virus (HIV) type 1 reverse transcriptase (RT) is an important target for therapeutic intervention and for HIV-1-specific cytotoxic T lymphocytes (CTL), An HLA-A2-restricted CTL epitope containing the sequence YMDD, which is highly conserved among human and animal retroviruses and essential for function of the RNA-dependent DNA polymerase, is identified, The drug resistance mutation at RT amino acid 184 (M184V), associated with (-)-2'-deoxy-3'-thiacytidine (lamivudine), (-)-2'-deoxy-5-fluoro-3'-thiacytidine (FTC), and dideoxyinosine resistance, is located within this epitope and abolishes recognition by an established CTL response, This study demonstrates that the CTL response may target functionally relevant regions of the RT protein and suggests drug therapy may select for viral variants with altered susceptibility to established cellular immune responses.
引用
收藏
页码:476 / 479
页数:4
相关论文
共 16 条
[1]   TREATMENT OF HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 (HIV-1)-INFECTED CELLS WITH COMBINATIONS OF HIV-1-SPECIFIC INHIBITORS RESULTS IN A DIFFERENT RESISTANCE PATTERN THAN DOES TREATMENT WITH SINGLE-DRUG THERAPY [J].
BALZARINI, J ;
KARLSSON, A ;
PEREZPEREZ, MJ ;
CAMARASA, MJ ;
TARPLEY, WG ;
DECLERCQ, E .
JOURNAL OF VIROLOGY, 1993, 67 (09) :5353-5359
[2]  
BOUCHER CA, 1993, 1ST NAT C HUM RETR R
[3]   CASSETTE MUTAGENESIS OF THE REVERSE-TRANSCRIPTASE OF HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 [J].
BOYER, PL ;
FERRIS, AL ;
HUGHES, SH .
JOURNAL OF VIROLOGY, 1992, 66 (02) :1031-1039
[4]   VIROLOGICAL AND IMMUNOLOGICAL CHARACTERIZATION OF LONG-TERM SURVIVORS OF HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 INFECTION [J].
CAO, YZ ;
QIN, LM ;
ZHANG, LQ ;
SAFRIT, J ;
HO, DD .
NEW ENGLAND JOURNAL OF MEDICINE, 1995, 332 (04) :201-208
[5]   HIV-1 DRUG-RESISTANCE - MOLECULAR PATHOGENESIS AND LABORATORY MONITORING [J].
DAQUILA, RT .
CLINICS IN LABORATORY MEDICINE, 1994, 14 (02) :393-422
[6]   IDENTIFICATION OF OVERLAPPING HLA CLASS I-RESTRICTED CYTOTOXIC T-CELL EPITOPES IN A CONSERVED REGION OF THE HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 ENVELOPE GLYCOPROTEIN - DEFINITION OF MINIMUM EPITOPES AND ANALYSIS OF THE EFFECTS OF SEQUENCE VARIATION [J].
JOHNSON, RP ;
TROCHA, A ;
BUCHANAN, TM ;
WALKER, BD .
JOURNAL OF EXPERIMENTAL MEDICINE, 1992, 175 (04) :961-971
[7]   BRIEF REPORT - ABSENCE OF INTACT NEF SEQUENCES IN A LONG-TERM SURVIVOR WITH NONPROGRESSIVE HIV-1 INFECTION [J].
KIRCHHOFF, F ;
GREENOUGH, TC ;
BRETTLER, DB ;
SULLIVAN, JL ;
DESROSIERS, RC .
NEW ENGLAND JOURNAL OF MEDICINE, 1995, 332 (04) :228-232
[8]   CONVERGENT COMBINATION THERAPY CAN SELECT VIABLE MULTIDRUG-RESISTANT HIV-1 IN-VITRO [J].
LARDER, BA ;
KELLAM, P ;
KEMP, SD .
NATURE, 1993, 365 (6445) :451-453
[9]   THE ANTIGENIC IDENTITY OF PEPTIDE-MHC COMPLEXES - A COMPARISON OF THE CONFORMATIONS OF 5 VIRAL PEPTIDES PRESENTED BY HLA-A2 [J].
MADDEN, DR ;
GARBOCZI, DN ;
WILEY, DC .
CELL, 1993, 75 (04) :693-708
[10]  
MADDEN DR, 1994, CELL, V76, P410