Analysis of MHC class II DP, DQ and DR alleles in Crohn's disease

被引:34
作者
Cariappa, A
Sands, B
Forcione, D
Finkelstein, D
Podolsky, DK
Pillai, S
机构
[1] Massachusetts Gen Hosp, Ctr Canc, Boston, MA 02129 USA
[2] Massachusetts Gen Hosp, Gastrointestinal Unit, Boston, MA 02129 USA
关键词
Crohn's disease; inflammatory bowel disease; genetic susceptibility; major histocompatibility complex; HLA class II genes;
D O I
10.1136/gut.43.2.210
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background-Although inflammation in Crohn's disease is believed to be mediated by activated T cells, genotyping of all MHC class II alleles in white people with this disease has not been reported. Aims-To perform a detailed molecular analysis of HLA DPB, DQB, and DRB genes in white patients with Crohn's disease and controls in order to determine if the inheritance of any class II genes confers susceptibility or resistance to this disease. Methods-Complete molecular typing of HLA class II DPB, DQB, and DRB alleles was performed in 58 white patients with Crohn's disease and 93 healthy controls using a polymerase chain reaction-sequence specific oligonucleotide based approach. Results-No significant association with any DPB or DQB alleles was noted in patients with Crohn's disease. Since our previous studies had shown a strong association of an HLA DRB3(star)0301/DRB1(star)1302 haplotype with Crohn's disease, we re-examined this association using more stringent genotyping criteria. This haplotype was present in 20.7% of patients and 5.4% of controls (p = 0.0066; relative risk = 4.59). Conclusions-The DRB3(star)0301/DRB1(star)1302 haplotype is the only significant MHC class II association noted in white people with Crohn's disease and represents the strongest association of any MHC or non-MHC locus with this disease.
引用
收藏
页码:210 / 215
页数:6
相关论文
共 27 条
  • [1] Association of HLA class II genes with susceptibility to Crohn's disease
    Danze, PM
    Colombel, JF
    Jacquot, S
    Loste, MN
    Heresbach, D
    Ategbo, S
    Khamassi, S
    Perichon, B
    Semana, G
    Charron, D
    Cezard, JP
    [J]. GUT, 1996, 39 (01) : 69 - 72
  • [2] DUERR RH, 1995, GASTROENTEROLOGY, V109, P1462
  • [3] An increased risk of Crohn's disease in individuals who inherit class II DRB3(*)0301 allele
    Forcione, DG
    Sands, B
    Isselbacher, KJ
    Rustgi, A
    Podolsky, DK
    Pillai, S
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (10) : 5094 - 5098
  • [4] OLIGONUCLEOTIDE GENOTYPING SHOWS THAT ALLELES AT THE HLA-DR-BETA-III LOCUS OF THE DRW52 SUPERTYPIC GROUP SEGREGATE INDEPENDENTLY OF KNOWN DR OR DW SPECIFICITIES
    GORSKI, J
    TILANUS, M
    GIPHART, M
    MACH, B
    [J]. IMMUNOGENETICS, 1987, 25 (02) : 79 - 83
  • [5] CROHNS-DISEASE IS ACCOMPANIED BY CHANGES IN THE CD4(+), BUT NOT CD8(+), T-CELL RECEPTOR BV REPERTOIRE OF LAMINA PROPRIA LYMPHOCYTES
    GULWANIAKOLKAR, B
    AKOLKAR, PN
    MCKINLEY, M
    FISHER, SE
    SILVER, J
    [J]. CLINICAL IMMUNOLOGY AND IMMUNOPATHOLOGY, 1995, 77 (01): : 95 - 106
  • [6] HERESBACH D, 1996, EUR J IMMUNOGENET, V23, P141
  • [7] Mapping of a susceptibility locus for Crohn's disease on chromosome 16
    Hugot, JP
    LaurentPuig, P
    GowerRousseau, C
    Olson, JM
    Lee, JC
    Beaugerie, L
    Naom, I
    Dupas, JL
    VanGossum, A
    Orholm, M
    BonaitiPellie, C
    Weissenbach, J
    Mathew, CG
    LennardJones, JE
    Cortot, A
    Colombel, JF
    Thomas, G
    [J]. NATURE, 1996, 379 (6568) : 821 - 823
  • [8] Imanishi T., 1992, HLA 1991, P1065
  • [9] Kimura A, 1992, HLA 1991, V1, P397
  • [10] MILLER WL, 1989, ANNU REV GENET, V23, P371, DOI 10.1146/annurev.ge.23.120189.002103