Duplicated DQ haplotypes increase the complexity of restriction element usage in cattle

被引:64
作者
Glass, EJ [1 ]
Oliver, RA [1 ]
Russell, GC [1 ]
机构
[1] Roslin Inst, Div Mol Biol, Roslin EH25 9PS, Midlothian, Scotland
关键词
D O I
10.4049/jimmunol.165.1.134
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 RMC of cattle encodes two distinct isotypes of class II molecules, DR and DQ, Unlike humans, cattle lack the DP locus and about half the common haplotypes express duplicated De genes. The number and frequency of DQA and DQB alleles means that most cattle are heterozygous. If inter- and/or intrahaplotype pairing of DQA and DQB molecules occurs, cattle carrying DQ-duplicated haplotypes may express more restriction elements than would be predicted by the number of expressed alleles, We are investigating whether duplicated haplotypes cause differences in immune response, particularly in terms of generating protective immunity. We have analyzed the Ag-presenting function of DQ molecules in two heterozygous animals, one of which carries a duplicated haplotype, We compared the class II isotype specificity of T cell clones recognizing a putative vaccinal peptide from foot-and-mouth disease virus (FMDV15). We show for the first time that bovine T cells can recognize Ag in the context of DQ molecules. We also present evidence that interhaplotype pairings of DQA and DQB molecules form functional restriction elements, Both animals showed distinct biases to usage of particular restriction elements. Mainly DQ-restricted clones were derived from the animal with duplicated DQ genes, whereas the majority of clones from the animal with a single DQ gene pair were DR restricted, Furthermore, haplotype bias was observed with both animals. These experiments show that understanding of class LI chain pairing in addition to knowledge of the genotype may be important in vaccine design where effective epitope selection is essential.
引用
收藏
页码:134 / 138
页数:5
相关论文
共 49 条
[1]  
Agrewala JN, 1998, CLIN EXP IMMUNOL, V114, P392
[2]   WHAT IS THE BASIS FOR HLA-DQ ASSOCIATIONS WITH AUTOIMMUNE-DISEASE [J].
ALTMANN, DM ;
SANSOM, D ;
MARSH, SGE .
IMMUNOLOGY TODAY, 1991, 12 (08) :267-270
[3]  
BALDWIN CL, 1987, COMP ASPECTS DIFFERE, P455
[4]   Analysis of genetic diversity at the DQA loci in African cattle: Evidence for a BoLA-DQA3 locus [J].
Ballingall, KT ;
Luyai, A ;
McKeever, DJ .
IMMUNOGENETICS, 1997, 46 (03) :237-244
[5]  
BALLINGALL KT, 1995, ANIM GENET, V26, P79, DOI 10.1111/j.1365-2052.1995.tb02637.x
[6]   Differential expression of major histocompatibility complex class II genes on murine macrophages associated with T cell cytokine profile and protective/suppressive effects [J].
Baumgart, M ;
Moos, V ;
Schuhbauer, D ;
Müller, B .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (12) :6936-6940
[7]   BIOCHEMICAL-CHARACTERIZATION OF BOVINE MHC DQ ALLELIC VARIANTS BY ONE-DIMENSIONAL ISOELECTRIC-FOCUSING [J].
BISSUMBHAR, B ;
NILSSON, PR ;
HENSEN, EJ ;
DAVIS, WC ;
JOOSTEN, I .
TISSUE ANTIGENS, 1994, 44 (02) :100-109
[8]  
BROOKS CF, 1988, IMMUNOLOGY, V63, P303
[9]   NEW APPROACHES TO VACCINATION AGAINST FOOT-AND-MOUTH-DISEASE [J].
BROWN, F .
VACCINE, 1992, 10 (14) :1022-1026
[10]  
CalvoCalle JM, 1997, J IMMUNOL, V159, P1362