HLA-B27 polymorphism and worldwide susceptibility to ankylosing spondylitis

被引:184
作者
GonzalezRoces, S
Alvarez, MV
Gonzalez, S
Dieye, A
Makni, H
Woodfield, DG
Housan, L
Konenkov, V
Abbadi, MC
Grunnet, N
Coto, E
LopezLarrea, C
机构
[1] HOSP CENT ASTURIAS,SERV IMMUNOL,E-33006 OVIEDO,SPAIN
[2] FAC MED SFAX,DEPT IMMUNOL,SFAX,TUNISIA
[3] AUCKLAND REG BLOOD BANK,DEPT TRANSFUS MED,AUCKLAND,NEW ZEALAND
[4] BEIJING MED UNIV,ARTHRITIS CLIN,PEOPLES HOSP,BEIJING,PEOPLES R CHINA
[5] INST CLIN IMMUNOL,SIBERIAN BRANCH,NOVOSIBIRSK,RUSSIA
[6] INST PASTEUR ALGERIE,DEPT IMMUNOL,TIPASA,ALGERIA
[7] INST PASTEUR,DEPT IMMUNOL,DAKAR,SENEGAL
[8] SKEJBY SYGEHUS,DEPT CLIN IMMUNOL,DK-8200 AARHUS,DENMARK
来源
TISSUE ANTIGENS | 1997年 / 49卷 / 02期
关键词
ankylosing spondylitis; B27; alleles; HLA and disease association; arthritogenic peptide;
D O I
10.1111/j.1399-0039.1997.tb02724.x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
HLA-B27 is strongly associated to ankylosing spondylitis (AS) and represents a family of eleven B27 alleles (B*2701-11). Our aim was to analyze the distribution of B27 subtypes by PCR/SSOP and genomic sequencing in a large group of populations (n = 17). 711 B27-positive samples from Caucasoid, Asian, African, Amerindian and Polynesian populations were selected to ascertain transracial gene mapping of the B27 subtypes. 476 of these were AS patients, chosen to investigate the contribution of B27 alleles to AS susceptibility. Some significant new findings have arisen from this study: 1) B*2705 was the predominant subtype in circumpolar and subarctic areas. B*2702 was found to be practically restricted to Caucasian populations, showing a higher frequency in Middle-East (Jews) and North Africa (Arabs/Berbers) groups. 2) B*2703 appears associated with AS in Western Africans. This is of remarkable interest since it was suggested that B*2703 would be negatively disease-associated. 3) Although B*2706 appears negatively associated with AS in Thais, we identified two patients from northern China carrying it. This may be a reflection of a disease heterogeneity and could indicate that more than one pathogenic agent can be involved in AS. B*2709 has been recently described as negatively associated with AS in Sardinians. The molecular changes His114Asp (B*2706) and Asp116His (B*2709) could modify the genetic susceptibility to AS.
引用
收藏
页码:116 / 123
页数:8
相关论文
共 36 条
  • [1] GUILT BY ASSOCIATION - HLA-B27 AND ANKYLOSING-SPONDYLITIS
    BENJAMIN, R
    PARHAM, P
    [J]. IMMUNOLOGY TODAY, 1990, 11 (04): : 137 - 142
  • [2] SUBTYPES OF HLA-B27 DETECTED BY CYTO-TOXIC LYMPHOCYTES-T AND THEIR ROLE IN SELF-RECOGNITION
    BREUNING, MH
    LUCAS, CJ
    BREUR, BS
    ENGELSMA, MY
    DELANGE, GG
    DEKKER, AJ
    BIDDISON, WE
    IVANYI, P
    [J]. HUMAN IMMUNOLOGY, 1982, 5 (04) : 259 - 268
  • [3] DISTRIBUTION OF HLA-B27 SUBTYPES IN PATIENTS WITH ANKYLOSING-SPONDYLITIS - THE DISEASE IS ASSOCIATED WITH A COMMON DETERMINANT OF THE VARIOUS B27 MOLECULES
    BREURVRIESENDORP, BS
    DEKKERSAEYS, AJ
    IVANYI, P
    [J]. ANNALS OF THE RHEUMATIC DISEASES, 1987, 46 (05) : 353 - 356
  • [4] DIFFERENT HLA-B27 SUBTYPES PRESENT THE SAME IMMUNODOMINANT EPSTEIN-BARR-VIRUS PEPTIDE
    BROOKS, JM
    MURRAY, RJ
    THOMAS, WA
    KURILLA, MG
    RICKINSON, AB
    [J]. JOURNAL OF EXPERIMENTAL MEDICINE, 1993, 178 (03) : 879 - 887
  • [5] ANCHORING POCKETS IN HUMAN HISTOCOMPATIBILITY COMPLEX LEUKOCYTE ANTIGEN (HLA) CLASS-I MOLECULES - ANALYSIS OF THE CONSERVED B-(45)-POCKET OF HLA-B27
    BUXTON, SE
    BENJAMIN, RJ
    CLAYBERGER, C
    PARHAM, P
    KRENSKY, AM
    [J]. JOURNAL OF EXPERIMENTAL MEDICINE, 1992, 175 (03) : 809 - 820
  • [6] Cavalli-Sforza L. L., 1994, The history and geography of human genes
  • [7] CHOO SY, 1988, HUM IMMUNOL, V21, P209
  • [8] CHOO SY, 1991, J IMMUNOL, V147, P174
  • [9] CHOO SY, 1986, IMMUNOGENETICS, V23, P24, DOI 10.1007/BF00376518
  • [10] CHOO SY, 1989, ANN INTERN MED, V111, P581