CHARACTERIZATION OF THE SPECIFICITY AND GENETIC RESTRICTION OF HUMAN CD4+ CYTOTOXIC T-CELL CLONES REACTIVE TO CAPSID ANTIGEN OF RUBELLA-VIRUS

被引:16
作者
OU, DW
CHONG, PL
MCVEISH, P
JEFFERIES, WA
GILLAM, S
机构
[1] UNIV BRITISH COLUMBIA, RES CTR, DEPT PATHOL, 950 W 28TH AVE, VANCOUVER V5Z 4H4, BC, CANADA
[2] CONNAUGHT CTR BIOTECHNOL RES, N YORK M2R 3T4, ONTARIO, CANADA
[3] UNIV BRITISH COLUMBIA, BIOTECHNOL LAB, VANCOUVER V6T 1W5, BC, CANADA
[4] UNIV BRITISH COLUMBIA, DEPT MED GENET, VANCOUVER V6T 1W5, BC, CANADA
[5] UNIV BRITISH COLUMBIA, DEPT MICROBIOL, VANCOUVER V6T 1W5, BC, CANADA
[6] UNIV BRITISH COLUMBIA, DEPT ZOOL, VANCOUVER V6T 1W5, BC, CANADA
基金
英国医学研究理事会; 加拿大自然科学与工程研究理事会;
关键词
D O I
10.1016/0042-6822(92)90243-I
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Using 11 overlapping synthetic peptides covering more than 95% of the amino acid sequence of capsid protein of rubella virus, 7 CD4+ T cell clones (R10, R11, R18, A2, A10, A1, and A12) isolated from 2 rubella seropositive donors reacted strongly to rubella capsid peptides C6 (residues 119-152), C9 (residues 205-233), or C11 (residues 255-280), respectively, in both proliferation and cytotoxicity assay. Truncated peptides C6E (residues 125-139), C9B (residues 205-216), and C11E (residues 260-272) were shown to be involved directly to the T cell determinants of C6, C9, and C11, respectively. Genetic restriction of these T cell clones was analyzed by using human cell lines with various HLA-DR phenotypes as targets and/or antigen-presenting cells in cytotoxicity assay and/or proliferation assays. The results indicated that the recognition of peptide C6 by T cell clones (R11 and R18) was associated with DRw9 molecule, while the HLA restriction element of the responses of other T cell clones (A2 and A11, A10, and A12) that reacted with peptide C9 or C11 was DR4 molecule. However, there may be a cross-recognition by the T cell clone (A12) between DR1 and DR4 subtypes. © 1992.
引用
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页码:680 / 686
页数:7
相关论文
共 29 条
[1]  
BERZOFSKY JA, 1989, VACCINES 89 MODERN A, P27
[2]  
BRETT SJ, 1991, J IMMUNOL, V147, P984
[3]  
BRODSKY FM, 1982, J IMMUNOL, V128, P129
[4]   RECOGNITION OF RABIES AND RABIES-RELATED VIRUSES BY T-CELLS DERIVED FROM HUMAN VACCINE RECIPIENTS [J].
CELIS, E ;
OU, D ;
DIETZSCHOLD, B ;
KOPROWSKI, H .
JOURNAL OF VIROLOGY, 1988, 62 (09) :3128-3134
[5]  
CELIS E, 1988, J IMMUNOL, V140, P1808
[6]  
CHANTLER JK, 1982, LANCET, V1, P1323
[7]   NUCLEOTIDE-SEQUENCE AND INVITRO EXPRESSION OF RUBELLA-VIRUS 24S SUBGENOMIC MESSENGER-RNA ENCODING THE STRUCTURAL PROTEIN-E1, PROTEIN-E2 AND PROTEIN-C [J].
CLARKE, DM ;
LOO, TW ;
HUI, I ;
CHONG, P ;
GILLAM, S .
NUCLEIC ACIDS RESEARCH, 1987, 15 (07) :3041-3057
[8]   T-CELL ANTIGENIC SITES TEND TO BE AMPHIPATHIC STRUCTURES [J].
DELISI, C ;
BERZOFSKY, JA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1985, 82 (20) :7048-7052
[9]  
FAYOLLE C, 1991, J IMMUNOL, V147, P4069
[10]  
FRASER JRE, 1983, CLIN EXP RHEUMATOL, V1, P287