FLAVIVIRUS-CROSS-REACTIVE, HLA-DR15-RESTRICTED EPITOPE ON NS3 RECOGNIZED BY HUMAN CD4(+) CD8(-) CYTOTOXIC T-LYMPHOCYTE CLONES

被引:54
作者
KURANE, I
OKAMOTO, Y
DAI, LC
ZENG, LL
BRINTON, MA
ENNIS, FA
机构
[1] UNIV MASSACHUSETTS,SCH MED,DEPT MED,DIV INFECT DIS & IMMUNOL,WORCESTER,MA 01655
[2] GEORGIA STATE UNIV,DEPT BIOL,ATLANTA,GA 30303
关键词
D O I
10.1099/0022-1317-76-9-2243
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The role of flavivirus-cross-reactive T lymphocytes in recovery from and pathogenesis of flavivirus infections is not known. In the present paper, we have defined a flavivirus-cross-reactive epitope recognized by two CD4(+) CD8(-) cytotoxic T lymphocyte (CTL) clones, JK4 and JK43. The T cell clones were established from the peripheral blood T lymphocytes of a dengue-4-immune donor, using a limiting-dilution method with dengue-4 antigen. These two T cell clones were cross-reactive for dengue virus types 1, 2, 3 and 4, yellow fever virus and West Nile virus, and recognized NS3 protein. The smallest synthetic peptide recognized by these T cell clones was an identical 9 amino acid peptide which contains amino acids 146 to 154 (VIGLYGNGV) of dengue-4 NS3. HLA-DR15 was the restriction allele for recognition of this epitope by JK4 and JK43. JK4 and JK43 both used T cell receptor V alpha 8, but JK4 used V beta 8 and JK43 used V beta 2. This result indicates that this epitope is recognized by two flavivirus-cross-reactive CD4(+) T cell clones which originated from different T cells in vivo.
引用
收藏
页码:2243 / 2249
页数:7
相关论文
共 32 条
[1]   NOMENCLATURE FOR FACTORS OF THE HLA SYSTEM, 1994 [J].
BODMER, JG ;
MARSH, SGE ;
ALBERT, ED ;
BODMER, WF ;
DUPONT, B ;
ERLICH, HA ;
MACH, B ;
MAYR, WR ;
PARHAM, P ;
SASAZUKI, T ;
SCHREUDER, GMT ;
STROMINGER, JL ;
SVEJGAARD, A ;
TERASAKI, PI .
HUMAN IMMUNOLOGY, 1994, 41 (01) :1-20
[2]   SEQUENCE-ANALYSIS OF THE VIRAL CORE PROTEIN AND THE MEMBRANE-ASSOCIATED PROTEIN-V1 AND PROTEIN-NV2 OF THE FLAVIVIRUS WEST NILE VIRUS AND OF THE GENOME SEQUENCE FOR THESE PROTEINS [J].
CASTLE, E ;
NOWAK, T ;
LEIDNER, U ;
WENGLER, G ;
WENGLER, G .
VIROLOGY, 1985, 145 (02) :227-236
[3]   FLAVIVIRUS GENOME ORGANIZATION, EXPRESSION, AND REPLICATION [J].
CHAMBERS, TJ ;
HAHN, CS ;
GALLER, R ;
RICE, CM .
ANNUAL REVIEW OF MICROBIOLOGY, 1990, 44 :649-688
[4]   SPECIFICITY AND PROMISCUITY AMONG NATURALLY PROCESSED PEPTIDES BOUND TO HLA-DR ALLELES [J].
CHICZ, RM ;
URBAN, RG ;
GORGA, JC ;
VIGNALI, DAA ;
LANE, WS ;
STROMINGER, JL .
JOURNAL OF EXPERIMENTAL MEDICINE, 1993, 178 (01) :27-47
[5]   HOW ALPHA-BETA-T-CELL RECEPTORS SEE PEPTIDE MHC COMPLEXES [J].
CHIEN, YH ;
DAVIS, MM .
IMMUNOLOGY TODAY, 1993, 14 (12) :597-602
[6]  
CHOMCZYNSKI P, 1987, ANAL BIOCHEM, V162, P156, DOI 10.1016/0003-2697(87)90021-2
[7]   NUCLEOTIDE AND COMPLETE AMINO-ACID SEQUENCES OF KUNJIN VIRUS - DEFINITIVE GENE ORDER AND CHARACTERISTICS OF THE VIRUS-SPECIFIED PROTEINS [J].
COIA, G ;
PARKER, MD ;
SPEIGHT, G ;
BYRNE, ME ;
WESTAWAY, EG .
JOURNAL OF GENERAL VIROLOGY, 1988, 69 :1-21
[8]   DENGUE VIRUS-SPECIFIC MEMORY T-CELL RESPONSES IN HUMAN VOLUNTEERS RECEIVING A LIVE ATTENUATED DENGUE VIRUS TYPE-2 CANDIDATE VACCINE [J].
DHARAKUL, T ;
KURANE, I ;
BHAMARAPRAVATI, N ;
YOKSAN, S ;
VAUGHN, DW ;
HOKE, CH ;
ENNIS, FA .
JOURNAL OF INFECTIOUS DISEASES, 1994, 170 (01) :27-33
[9]   FULL-LENGTH CDNA SEQUENCE OF DENGUE TYPE-1 VIRUS (SINGAPORE STRAIN S275/90) [J].
FU, JL ;
TAN, BH ;
YAP, EH ;
CHAN, YC ;
TAN, YH .
VIROLOGY, 1992, 188 (02) :953-958
[10]   DENGUE VIRUS-SPECIFIC HUMAN CD4+ T-LYMPHOCYTE RESPONSES IN A RECIPIENT OF AN EXPERIMENTAL LIVE-ATTENUATED DENGUE VIRUS TYPE-1 VACCINE - BULK CULTURE PROLIFERATION, CLONAL ANALYSIS, AND PRECURSOR FREQUENCY DETERMINATION [J].
GREEN, S ;
KURANE, I ;
EDELMAN, R ;
TACKET, CO ;
ECKELS, KH ;
VAUGHN, DW ;
HOKE, CH ;
ENNIS, FA .
JOURNAL OF VIROLOGY, 1993, 67 (10) :5962-5967