Heterotypic recognition of recombinant FMDV proteins by bovine T-cells:: the polymerase (P3Dpol) as an immunodominant T-cell immunogen

被引:40
作者
Collen, T
Baron, J
Childerstone, A
Corteyn, A
Doel, TR
Flint, M
Garcia-Valcarcel, M
Parkhouse, RME
Ryan, MD
机构
[1] AFRC, Inst Anim Hlth, Dept Immunol, Surrey GU24 0NF, England
[2] Inst Anim Hlth, Dept Biol Mol, Surrey GU24 0NF, England
[3] Inst Anim Hlth, Dept Pathol & Immunol, Compton RG20 7NN, Berks, England
[4] Rhone Merieur, Surrey GU24 0NE, England
[5] Univ Reading, Sch Anim & Microbial Sci, Reading RG6 6AL, Berks, England
[6] British Biotechnol Ltd, Immunotherapeut Div, Oxford OX4 5LY, England
[7] Univ St Andrews, Div Cell & Mol Biol, St Andrews KY16 9AL, Fife, Scotland
关键词
foot-and-mouth disease virus; T-cell recognition; serotype-cross-reactivity; RNA-dependent RNA polymerase;
D O I
10.1016/S0168-1702(98)00035-5
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
In this study we have examined the recognition of VP0, VP1, VP2, VP3 and P3D(pol) by PBMC and CD4(+) T-cells from infected, vaccinated-challenged, and multiply-vaccinated (O1, A24, C1 or ASIA1) cattle using recombinant proteins of an O1 serotype virus. The structural protein VPI was recognised in an homotypic context whereas VP2, VP3, VP4 and P3D(pol) were also recognised by T-cells from animals exposed to heterotypic viruses. Only the non-structural protein P3D(pol) was consistently recognised by T-cells from the majority of animals examined and heterotypic recognition correlated with the presence of serologically detectable P3D(pol) ii: purified virus. Thus, P3D(pol) is a major cross-reactive immunodeterminant of FMDV, eliciting heterotypic T-cell responses and, therefore, with possible potential for inclusion in a subunit vaccine. (C) 1998 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:125 / 133
页数:9
相关论文
共 38 条
[1]   THE IMMUNE-RESPONSE OF BALB C MICE TO INFLUENZA HEMAGGLUTININ - COMMONALITY OF THE B-CELL AND T-CELL REPERTOIRES AND THEIR RELEVANCE TO ANTIGENIC DRIFT [J].
BARNETT, BC ;
GRAHAM, CM ;
BURT, DS ;
SKEHEL, JJ ;
THOMAS, DB .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1989, 19 (03) :515-521
[2]   IMMUNE-MECHANISMS IN CONTACT ALLERGIC DERMATITIS [J].
BERGSTRESSER, PR .
DERMATOLOGIC CLINICS, 1990, 8 (01) :3-11
[3]   PROTECTION AGAINST FOOT-AND-MOUTH-DISEASE BY IMMUNIZATION WITH A CHEMICALLY SYNTHESIZED PEPTIDE PREDICTED FROM THE VIRAL NUCLEOTIDE-SEQUENCE [J].
BITTLE, JL ;
HOUGHTEN, RA ;
ALEXANDER, H ;
SHINNICK, TM ;
SUTCLIFFE, JG ;
LERNER, RA ;
ROWLANDS, DJ ;
BROWN, F .
NATURE, 1982, 298 (5869) :30-33
[4]   FUSION PROTEINS WITH MULTIPLE COPIES OF THE MAJOR ANTIGENIC DETERMINANT OF FOOT-AND-MOUTH-DISEASE VIRUS PROTECT BOTH THE NATURAL HOST AND LABORATORY-ANIMALS [J].
BROEKHUIJSEN, MP ;
VANRIJN, JMM ;
BLOM, AJM ;
POUWELS, PH ;
ENGERVALK, BE ;
BROWN, F ;
FRANCIS, MJ .
JOURNAL OF GENERAL VIROLOGY, 1987, 68 :3137-3143
[5]   IMPROVED IMMUNOGENICITY OF A PEPTIDE EPITOPE AFTER FUSION TO HEPATITIS-B CORE PROTEIN [J].
CLARKE, BE ;
NEWTON, SE ;
CARROLL, AR ;
FRANCIS, MJ ;
APPLEYARD, G ;
SYRED, AD ;
HIGHFIELD, PE ;
ROWLANDS, DJ ;
BROWN, F .
NATURE, 1987, 330 (6146) :381-384
[6]   HETEROTYPIC RECOGNITION OF FOOT-AND-MOUTH-DISEASE VIRUS BY CATTLE LYMPHOCYTES [J].
COLLEN, T ;
DOEL, TR .
JOURNAL OF GENERAL VIROLOGY, 1990, 71 :309-315
[7]   INDUCTION OF ANTIBODY TO FOOT-AND-MOUTH-DISEASE VIRUS IN PRESENSITIZED MOUSE SPLEEN-CELL CULTURES [J].
COLLEN, T ;
MCCULLOUGH, KC ;
DOEL, TR .
JOURNAL OF VIROLOGY, 1984, 52 (02) :650-655
[8]  
COLLEN T, 1991, J IMMUNOL, V146, P749
[9]   A 3RD ANTIGENIC COMPONENT ASSOCIATED WITH FOOT-AND-MOUTH DISEASE INFECTION [J].
COWAN, KM ;
GRAVES, JH .
VIROLOGY, 1966, 30 (03) :528-+
[10]  
DAWE PS, 1978, BRIT VET J, V134, P504