Establishment and characterization of NS3 protein-specific T-cell clones from a patient with chronic hepatitis C

被引:7
作者
Chiang, BL
Yang, PM
Hwang, LH
Wang, JM
Kao, SF
Pan, CH
Chi, WK
Chen, PJ
Chen, DS
机构
[1] Natl Taiwan Univ Hosp, Coll Med, Hepatitis Res Ctr, Taipei 100, Taiwan
[2] Natl Taiwan Univ Hosp, Coll Med, Grad Inst Clin Med, Taipei 100, Taiwan
[3] Natl Taiwan Univ Hosp, Coll Med, Dept Internal Med, Taipei 100, Taiwan
[4] Dev Ctr Biotechnol, Proc Dev Div, Taipei, Taiwan
关键词
hepatitis C virus; T-cell clones; cytokines;
D O I
10.1007/BF02255861
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Our previous study showed dominant proliferative response of peripheral mononuclear cells to hepatitis C virus (HCV) nonstructural (NS-3) (T9, from aa 1188 to 1493) in chronically infected patients. Six T9-specific T-cell clones derived in an HCV patient were established and studied for the antigen specificity and the ability of augmentation of in vitro antibody production. All these cloned T-cell lines responded exclusively to T9 antigen and could help autologous B cells in producing anti-T9 antibody in vitro. Cytokine mRNAs of these T cells was detected by polymerase chain reaction and predominant IL-2 and IFN-gamma production was noted. In addition, further elucidation of T-cell antigenic determinant and MHC restriction suggested that these T-cell clones recognized at least two different T-cell antigenic determinants within the NS-3 region in an HLA DQ2-restricted manner. We believe characterization of HCV-specific T-cell responses, especially T-cell epitope mapping and cytokine production pattern, may shed light on further understanding the pathogenic mechanism and designing therapy for HCV infection.
引用
收藏
页码:290 / 296
页数:7
相关论文
共 29 条
[21]   TYPING HEPATITIS-C VIRUS BY POLYMERASE CHAIN-REACTION WITH TYPE-SPECIFIC PRIMERS - APPLICATION TO CLINICAL SURVEYS AND TRACING INFECTIOUS SOURCES [J].
OKAMOTO, H ;
SUGIYAMA, Y ;
OKADA, S ;
KURAI, K ;
AKAHANE, Y ;
SUGAI, Y ;
TANAKA, T ;
SATO, K ;
TSUDA, F ;
MIYAKAWA, Y ;
MAYUMI, M .
JOURNAL OF GENERAL VIROLOGY, 1992, 73 :673-679
[22]   FULL-LENGTH SEQUENCE OF A HEPATITIS-C VIRUS GENOME HAVING POOR HOMOLOGY TO REPORTED ISOLATES - COMPARATIVE-STUDY OF 4 DISTINCT GENOTYPES [J].
OKAMOTO, H ;
KURAI, K ;
OKADA, SI ;
YAMAMOTO, K ;
LIZUKA, H ;
TANAKA, T ;
FUKUDA, S ;
TSUDA, F ;
MISHIRO, S .
VIROLOGY, 1992, 188 (01) :331-341
[23]   PHENOTYPIC AND FUNCTIONAL-HETEROGENEITY OF CD4+ T-CELLS [J].
POWRIE, F ;
MASON, D .
IMMUNOLOGY TODAY, 1988, 9 (09) :274-277
[24]   T-CELL AND CYTOKINE RESPONSES IN LEISHMANIASIS [J].
REED, SG ;
SCOTT, P .
CURRENT OPINION IN IMMUNOLOGY, 1993, 5 (04) :524-531
[25]  
SCHUPPER H, 1993, HEPATOLOGY, V18, P1055
[26]   AN EPITOPE IN HEPATITIS-C VIRUS CORE REGION RECOGNIZED BY CYTOTOXIC T-CELLS IN MICE AND HUMANS [J].
SHIRAI, M ;
OKADA, H ;
NISHIOKA, M ;
AKATSUKA, T ;
WYCHOWSKI, C ;
HOUGHTEN, R ;
PENDLETON, CD ;
FEINSTONE, SM ;
BERZOFSKY, JA .
JOURNAL OF VIROLOGY, 1994, 68 (05) :3334-3342
[27]   APPLICATION OF ANIMAL TOXICOLOGY DATA TO CLINICAL-STUDY OF EXPERIMENTAL DRUGS [J].
TOMASZEWSKI, KE .
COMPARATIVE HAEMATOLOGY INTERNATIONAL, 1993, 3 (02) :67-70
[28]   EVIDENCE FOR IMMUNE SELECTION OF HEPATITIS-C VIRUS (HCV) PUTATIVE ENVELOPE GLYCOPROTEIN VARIANTS - POTENTIAL ROLE IN CHRONIC HCV INFECTIONS [J].
WEINER, AJ ;
GEYSEN, HM ;
CHRISTOPHERSON, C ;
HALL, JE ;
MASON, TJ ;
SARACCO, G ;
BONINO, F ;
CRAWFORD, K ;
MARION, CD ;
CRAWFORD, KA ;
BRUNETTO, M ;
BARR, PJ ;
MIYAMURA, T ;
MCHUTCHINSON, J ;
HOUGHTON, M .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (08) :3468-3472
[29]  
YANG JH, 1995, CHINESE J CHEM ENG, V3, P101