CENTRAL MHC GENES, IGA DEFICIENCY AND AUTOIMMUNE-DISEASE

被引:93
作者
FRENCH, MAH
DAWKINS, RL
机构
[1] UNIV WESTERN AUSTRALIA,DEPT CLIN IMMUNOL,NEDLANDS,WA 6009,AUSTRALIA
[2] SIR CHARLES GAIRDNER HOSP,DEPT CLIN IMMUNOL,NEDLANDS,WA 6009,AUSTRALIA
来源
IMMUNOLOGY TODAY | 1990年 / 11卷 / 08期
关键词
D O I
10.1016/0167-5699(90)90110-U
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
IgA deficiency is a common immunological disorder that is sometimes associated with an immunodeficiency syndrome, allergic disease, autoimmune disease and gluten enteropathy. Many subjects with this deficiency, however, are healthy, at least for many decades. Analysis of the immunological and genetic abnormalities found in IgA deficiency and in some of the associated disorders has led to the postulate that a genetically determined defect of immunoregulation underlies all of these diseases. Here, Martyn French and Roger Dawkins propose that the products of genes located within the central region of the major histocompatibility complex (MHC) regulate B cells and/or antibody production. Particular MHC ancestral haplotypes contain specific alleles and arrangements of these genes, thereby explaining associations with either increased or decreased production of immunoglobulin isotypes by B cells. © 1990.
引用
收藏
页码:271 / 274
页数:4
相关论文
共 52 条
[1]  
ALPER C A, 1987, Complement, V4, P125
[2]  
ASHERSON GL, 1980, DIAGNOSIS TREATMENT, P99
[3]  
ASQUITH P, 1974, CLIN GASTROENTEROL, V3, P213
[4]  
BACLE F, 1990, J IMMUNOL, V144, P147
[5]  
BEHAN PO, 1976, LANCET, P593
[6]   THE REGULATION OF IGG SUBCLASS PRODUCTION IN MAN - LOW SERUM IGG4 IN INHERITED DEFICIENCIES OF THE CLASSICAL PATHWAY OF C-3 ACTIVATION [J].
BIRD, P ;
LACHMANN, PJ .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1988, 18 (08) :1217-1222
[7]  
BOTTGER EC, 1987, IMMUNOL TODAY, V8, P261, DOI 10.1016/0167-5699(87)90184-8
[8]  
CASSIDY JT, 1979, CLIN EXP IMMUNOL, V35, P296
[9]  
CASSIDY JT, 1969, NEW ENGL J MED, V280, P275
[10]  
COBAIN TJ, 1983, TISSUE ANTIGENS, V22, P151