Predominance of HLA-restricted cytotoxic T-lymphocyte responses to serotype-cross-reactive epitopes on nonstructural proteins following natural secondary dengue virus infection

被引:93
作者
Mathew, A
Kurane, I
Green, S
Stephens, HAF
Vaughn, DW
Kalayanarooj, S
Suntayakorn, S
Chandanayingyong, D
Ennis, FA
Rothman, AL
机构
[1] Univ Massachusetts, Med Ctr, Ctr Infect Dis & Vaccine Res, Worcester, MA 01655 USA
[2] Middlesex Hosp, Div Nephrol, London, England
[3] Queen Sirikit Natl Inst Child Hlth, Armed Forces Res Inst Med Sci, Dept Virol, Bangkok, Thailand
[4] Siriraj Hosp, Dept Transfus Med, Bangkok, Thailand
[5] Kamphaeng Phet Prov Hosp, Kamphaeng Phet, Thailand
关键词
D O I
10.1128/JVI.72.5.3999-4004.1998
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
We examined the memory cytotoxic T-lymphocytic (CTL) responses of peripheral blood mononuclear cells (PBMC) obtained from patients in Thailand 12 months after natural symptomatic secondary dengue virus infection. In all four patients analyzed, CTLs were detected in bulk culture PBMC against nonstructural dengue virus proteins, Numerous CD4(+) and CD8(+) CTL lines were generated from the bulk cultures of two patients, KPP94-037 and KPP94-024, which were specific for NS1.2a (NS1 and NS2a collectively) and NS3 proteins, respectively. All CTL lines derived from both patients were cross-reactive with other serotypes of dengue virus. The CD8(+) NS1.2a-specific lines from patient KPP94-037 were HLA B57 restricted, and the CD8(+) NS3-specific lines from patient KPP93-024 were HLA B7 restricted. The CD4(+) CTL lines from patient KPP94-037 were HLA DR7 restricted. A majority of the CD8(+) CTLs isolated from patient KPP93-024 were found to recognize amino acids 221 to 232 on NS3, These results demonstrate that in Thai patients after symptomatic secondary natural dengue infections, CTLs are mainly directed against nonstructural proteins and are broadly cross-reactive.
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页码:3999 / 4004
页数:6
相关论文
共 23 条
[1]   THE ESSENCE OF EPITOPES [J].
BARBER, LD ;
PARHAM, P .
JOURNAL OF EXPERIMENTAL MEDICINE, 1994, 180 (04) :1191-1194
[2]   DENGUE VIRUS-SPECIFIC CROSS-REACTIVE CD8+ HUMAN CYTO-TOXIC T-LYMPHOCYTES [J].
BUKOWSKI, JF ;
KURANE, I ;
LAI, CJ ;
BRAY, M ;
FALGOUT, B ;
ENNIS, FA .
JOURNAL OF VIROLOGY, 1989, 63 (12) :5086-5091
[3]   HLA-A, -B, -DRB1, -DQA1, and -DQB1 polymorphism in Thais [J].
Chandanayingyong, D ;
Stephens, HAF ;
Klaythong, R ;
Sirikong, M ;
Udee, S ;
Longta, P ;
Chantangpol, R ;
Bejrachandra, S ;
Rungruang, E .
HUMAN IMMUNOLOGY, 1997, 53 (02) :174-182
[4]  
CHIEWSLIP P, 1981, AM J TROP MED HYG, V30, P1101
[5]   PROPER PROCESSING OF DENGUE VIRUS NONSTRUCTURAL GLYCOPROTEIN-NS1 REQUIRES THE N-TERMINAL HYDROPHOBIC SIGNAL SEQUENCE AND THE DOWNSTREAM NONSTRUCTURAL PROTEIN-NS2A [J].
FALGOUT, B ;
CHANOCK, R ;
LAI, CJ .
JOURNAL OF VIROLOGY, 1989, 63 (05) :1852-1860
[6]   Identification of two epitopes on the dengue 4 virus capsid protein recognized by a serotype-specific and a panel of serotype-cross-reactive human CD4(+) cytotoxic T-Lymphocyte clones [J].
Gagnon, SJ ;
Zeng, WL ;
Kurane, I ;
Ennis, FA .
JOURNAL OF VIROLOGY, 1996, 70 (01) :141-147
[7]   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
[8]  
HALSTEAD SB, 1970, YALE J BIOL MED, V42, P311
[9]  
HALSTEAD SB, 1988, TOGAVIRUSES BIOL STR, P107
[10]  
KALYANAROOJ S, 1997, J INFECT DIS, V176, P313