Mapping the T cell epitopes of the Babesia bovis antigen 12D3:: implications for vaccine design

被引:8
作者
Court, RA
Sitte, K
Opdebeeck, JP
East, IJ
机构
[1] CSIRO, Div Trop Anim Prod, CRC Vaccine Technol, Indooroopilly, Qld 4068, Australia
[2] Queensland Inst Med Res, CRC Vaccine Technol, Herston, Qld 4029, Australia
[3] Univ Queensland, Dept Parasitol, Brisbane, Qld 4067, Australia
关键词
Babesia bovis; 12D3; antigen; T-cell epitopes; vaccine design;
D O I
10.1046/j.1365-3024.1998.t01-1-00116.x
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The Babesia bovis antigen 12D3 was analysed to identify, potential T-cell epitopes. Two predictive algorithms identified 13 possible sites but, there was minimal agreement between the different predictive methods. Experimental determination of the T-cell epitopes recognized by nine cattle was achieved using a panel of overlapping peptides which identified Seven different epitopes, five of which were clustered together around residues 210-320 of the molecule. No T cell epitopes were located within the tightly disulphide bonded core of 12D3. Using a series of truncated peptides, the location of two of the epitopes was mapped to residues 35-43 and 266-275. The sequences of these two epitopes was compared with a database of previously described binding motifs for MHC II alleles and each epitope was found to contain three sequence motifs recognized by HLA-DR alleles. The BoLA-DRB3 alleles occurring in these cattle were determined by a sequence specific oligonucleotide hybridization assay. Within those cattle whose T cells proliferated in response to 12D3, there was a consistent pattern of epitope recognition and presence of particular DRB3 alleles. The implications for effective vaccine design are discussed.
引用
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页码:1 / 8
页数:8
相关论文
共 34 条
[1]   GENETIC PREDICTION OF NONRESPONSE TO HEPATITIS-B VACCINE [J].
ALPER, CA ;
KRUSKALL, MS ;
MARCUSBAGLEY, D ;
CRAVEN, DE ;
KATZ, AJ ;
BRINK, SJ ;
DIENSTAG, JL ;
AWDEH, Z ;
YUNIS, EJ .
NEW ENGLAND JOURNAL OF MEDICINE, 1989, 321 (11) :708-712
[2]   EVOLUTION OF MHC POLYMORPHISM - EXTENSIVE SHARING OF POLYMORPHIC SEQUENCE MOTIFS BETWEEN HUMAN AND BOVINE DRB ALLELES [J].
ANDERSSON, L ;
SIGURDARDOTTIR, S ;
BORSCH, C ;
GUSTAFSSON, K .
IMMUNOGENETICS, 1991, 33 (03) :188-193
[3]   INVESTIGATIONS OF BREAKDOWNS IN PROTECTION PROVIDED BY LIVING BABESIA-BOVIS VACCINE [J].
BOCK, RE ;
DEVOS, AJ ;
KINGSTON, TG ;
SHIELS, IA ;
DALGLIESH, RJ .
VETERINARY PARASITOLOGY, 1992, 43 (1-2) :45-56
[4]   MHCPEP - A DATABASE OF MHC-BINDING PEPTIDES [J].
BRUSIC, V ;
RUDY, G ;
HARRISON, LC .
NUCLEIC ACIDS RESEARCH, 1994, 22 (17) :3663-3665
[5]  
Callow L. L., 1971, Proceedings 19th World Veterinary Congress, Mexico City, V1, P357
[6]   REDUCTION IN VIRULENCE OF BABESIA-BOVIS DUE TO RAPID PASSAGE IN SPLENECTOMIZED CATTLE [J].
CALLOW, LL ;
MELLORS, LT ;
MCGREGOR, W .
INTERNATIONAL JOURNAL FOR PARASITOLOGY, 1979, 9 (04) :333-338
[7]   Heterologous expression of the cuticular glutathione peroxidase of lymphatic filariae in an attenuated vaccine strain of Salmonella typhimurium abrogates H-2 restriction of specific antibody responses [J].
Chacon, MR ;
Londono, P ;
Dougan, G ;
Selkirk, ME .
PARASITE IMMUNOLOGY, 1996, 18 (06) :307-316
[8]   Peripheral blood lymphocyte proliferative responses in cattle infected with or vaccinated against Anaplasma marginale [J].
Gale, KR ;
Gartside, MG ;
Dimmock, CM ;
Zakrzewski, H ;
Leatch, G .
PARASITOLOGY RESEARCH, 1996, 82 (06) :551-562
[9]   STRATEGIES FOR EPITOPE ANALYSIS USING PEPTIDE-SYNTHESIS [J].
GEYSEN, HM ;
RODDA, SJ ;
MASON, TJ ;
TRIBBICK, G ;
SCHOOFS, PG .
JOURNAL OF IMMUNOLOGICAL METHODS, 1987, 102 (02) :259-274
[10]  
HARPER G, 1996, IN PRESS INT J PARAS