Primary adenovirus-specific cytotoxic T lymphocyte response occurs after viral clearance and liver enzyme elevation

被引:16
作者
Chen, J
Zajac, AJ
McPherson, SA
Hsu, HC
Yang, P
Wu, Q
Xu, X
Wang, X
Fujihashi, K
Curiel, DT
Mountz, JD
机构
[1] Univ Alabama, Dept Med, Div Clin Immunol & Rheumatol, Birmingham, AL 35294 USA
[2] Univ Alabama, Dept Microbiol, Birmingham, AL 35294 USA
[3] Univ Alabama, Ctr AIDS Res, Birmingham, AL 35294 USA
[4] Univ Alabama, Dept Pediat Dent, Birmingham, AL 35294 USA
[5] Univ Alabama, Dept Pathol & Surg, Birmingham, AL 35294 USA
[6] Univ Alabama, Div Human Gene Therapy, Birmingham, AL 35294 USA
[7] Univ Alabama, Gene Therapy Ctr, Birmingham, AL 35294 USA
[8] Vet Adm Med Ctr, Birmingham, AL USA
关键词
adenovirus; cytotoxic T lymphocyte response; class I MHC tetramer; viral clearance; liver enzyme elevation;
D O I
10.1038/sj.gt.3302494
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The virus-specific cytotoxic T lymphocyte (CTL) response is a major obstacle to effective delivery of adenovirus gene therapy. However, its relative role in viral clearance, transgene elimination and hepatotoxicity remains unclear. In this paper, we present an analysis of viral clearance and liver toxicity in relation to the induction of the virus-specific CD8 T-cell response revealed by an MHC class I tetramer. A surprisingly high number of tetramer(+) CD8 T cells were found in the liver and lung and reached peak values at days 8 and 10, respectively, post-infection. Nearly 100% of these tetramer(+) CD8 T cells expressed high levels of granzyme B and IFN gamma. Remarkably, liver viral load and liver enzyme elevation peaked early, at days 2 and 4, respectively, postinfection, before the specific CTL response was detectable. After generation of CTLs, there was only minimal liver damage or further decrease in virus titer. These results indicated that the primary peak response of tetramer(+) CTLs does not correlate with the elimination of adenovirus or liver cytotoxic response.
引用
收藏
页码:1079 / 1088
页数:10
相关论文
共 46 条
[1]   Phenotypic analysis of antigen-specific T lymphocytes [J].
Altman, JD ;
Moss, PAH ;
Goulder, PJR ;
Barouch, DH ;
McHeyzerWilliams, MG ;
Bell, JI ;
McMichael, AJ ;
Davis, MM .
SCIENCE, 1996, 274 (5284) :94-96
[2]   Characteristics of virus-specific CD8+ T cells in the liver during the control and resolution phases of influenza pneumonia [J].
Belz, GT ;
Altman, JD ;
Doherty, PC .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (23) :13812-13817
[3]   Interactions between the immune system and gene therapy vectors: Bidirectional regulation of response and expression [J].
Bromberg, JS ;
Debruyne, LA ;
Qin, LH .
ADVANCES IN IMMUNOLOGY, VOL 69, 1998, 69 :353-409
[4]   Ablation of CD8 and CD4 T cell responses by high viral loads [J].
Fuller, MJ ;
Zajac, AJ .
JOURNAL OF IMMUNOLOGY, 2003, 170 (01) :477-486
[5]   Cytokine requirements for acute and basal homeostatic proliferation of naive and memory CD8+ T cells [J].
Goldrath, AW ;
Sivakumar, PV ;
Glaccum, M ;
Kennedy, MK ;
Bevan, MJ ;
Benoist, C ;
Mathis, D ;
Butz, EA .
JOURNAL OF EXPERIMENTAL MEDICINE, 2002, 195 (12) :1515-1522
[6]   CD4+CD25+ regulatory T cells inhibit immune-mediated transgene rejection [J].
Gross, DA ;
Leboeuf, M ;
Gjata, B ;
Danos, O ;
Davoust, J .
BLOOD, 2003, 102 (13) :4326-4328
[7]  
Hackett NR, 2000, CURR OPIN MOL THER, V2, P376
[8]   CD8+ T cell effector mechanisms in resistance to infection [J].
Harty, JT ;
Tvinnereim, AR ;
White, DW .
ANNUAL REVIEW OF IMMUNOLOGY, 2000, 18 :275-308
[9]   Immunity to adenovirus and adeno-associated viral vectors: implications for gene therapy [J].
Jooss, K ;
Chirmule, N .
GENE THERAPY, 2003, 10 (11) :955-963
[10]   Selective expression of the interleukin 7 receptor identifies effector CD8 T cells that give rise to long-lived memory cells [J].
Kaech, SM ;
Tan, JT ;
Wherry, EJ ;
Konieczny, BT ;
Surh, CD ;
Ahmed, R .
NATURE IMMUNOLOGY, 2003, 4 (12) :1191-1198