The attachment (G) glycoprotein of respiratory syncytial virus contains a single immunodominant epitope that elicits both Th1 and Th2CD4+ T cell responses

被引:98
作者
Varga, SM
Wissinger, EL
Braciale, TJ
机构
[1] Univ Virginia, Beirne Carter Ctr Immunol Res, Charlottesville, VA 22908 USA
[2] Univ Virginia, Hlth Sci Ctr, Dept Microbiol, Charlottesville, VA 22908 USA
[3] Univ Virginia, Hlth Sci Ctr, Dept Pathol, Charlottesville, VA 22908 USA
关键词
D O I
10.4049/jimmunol.165.11.6487
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
BALB/c mice immunized with a vaccinia virus expressing the attachment (G) glycoprotein of respiratory syncytial virus (RSV) develop a virus-specific CD4(+) T cell response that consists of a mixture of Thf and Th2 CD4(+) T cells following intranasal infection with live RSV, Recent work has shown that both Th1 and Th2 CD4(+) T cells are elicited to a single region comprising aa 183-197 of the G protein. To more precisely define the CD4(+) T cell epitope(s) contained within this region, we created a panel of amino- and carboxyl-terminal truncated as well as single alanine-substituted peptides spanning aa 183-197, These peptides were used to examine the ex vivo cytokine response of memory effector CD4(+) T cells infiltrating the lungs of G-primed RSV-infected mice. Analysis of lung-derived memory effector CD4(+) T cells using intracellular cytokine staining and/or ELISA of effector T cell culture supernatants revealed a single I-E-d-restricted CD4(+) T cell epitope with a core sequence mapping to aa 185-193, In addition, we examined the T cell repertoire of the RSV G peptide-specific CD4(+) T cells and show that the CD4(+) T cells directed-to this single immunodominant G epitope use a restricted range of TCR V beta genes and predominantly express V beta 14 TCR.
引用
收藏
页码:6487 / 6495
页数:9
相关论文
共 70 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]   DISTINCT PATTERNS OF T-CELL AND B-CELL IMMUNITY TO RESPIRATORY SYNCYTIAL VIRUS-INDUCED BY INDIVIDUAL VIRAL-PROTEINS [J].
ALWAN, WH ;
OPENSHAW, PJM .
VACCINE, 1993, 11 (04) :431-437
[3]   DISTINCT TYPES OF LUNG-DISEASE CAUSED BY FUNCTIONAL SUBSETS OF ANTIVIRAL T-CELLS [J].
ALWAN, WH ;
KOZLOWSKA, WJ ;
OPENSHAW, PJM .
JOURNAL OF EXPERIMENTAL MEDICINE, 1994, 179 (01) :81-89
[4]  
ALWAN WH, 1992, CLIN EXP IMMUNOL, V88, P527
[5]   EXPRESSION OF THE MAJOR GLYCOPROTEIN-G OF HUMAN RESPIRATORY SYNCYTIAL VIRUS FROM RECOMBINANT VACCINIA VIRUS VECTORS [J].
BALL, LA ;
YOUNG, KKY ;
ANDERSON, K ;
COLLINS, PL ;
WERTZ, GW .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1986, 83 (02) :246-250
[6]   PARENTERAL ADMINISTRATION OF LIVE RESPIRATORY SYNCYTIAL VIRUS-VACCINE - RESULTS OF A FIELD TRIAL [J].
BELSHE, RB ;
VANVORIS, LP ;
MUFSON, MA .
JOURNAL OF INFECTIOUS DISEASES, 1982, 145 (03) :311-319
[7]   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
[8]  
Bieganowska K, 1999, J IMMUNOL, V162, P1765
[9]   Helper T cell differentiation is controlled by the cell cycle [J].
Bird, JJ ;
Brown, DR ;
Mullen, AC ;
Moskowitz, NH ;
Mahowald, MA ;
Sider, JR ;
Gajewski, TF ;
Wang, CR ;
Reiner, SL .
IMMUNITY, 1998, 9 (02) :229-237
[10]   CYTOKINES IN THE GENERATION OF IMMUNE-RESPONSES TO, AND RESOLUTION OF, VIRUS-INFECTION [J].
BIRON, CA .
CURRENT OPINION IN IMMUNOLOGY, 1994, 6 (04) :530-538