Contribution of DRB1*04 variants to predisposition to or protection from insulin dependent diabetes mellitus is independent of DQ

被引:28
作者
HarfouchHammoud, E
Timsit, J
Boitard, C
Bach, JF
CaillatZucman, S
机构
[1] HOP NECKER ENFANTS MALAD,INSERM,U25,F-75015 PARIS,FRANCE
[2] HOP NECKER ENFANTS MALAD,SERV IMMUNOL CLIN,F-75015 PARIS,FRANCE
关键词
HLA class II; IDDM susceptibility; genetic predisposition; DR4; genotyping;
D O I
10.1006/jaut.1996.0056
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Certain DQ alpha/beta dimeric molecules have been shown to play a major role in determining susceptibility or resistance to IDDM. Whether or not predisposition associated with DR4 haplotypes is exclusively due to linkage to DQB1*0302 and DQA1*0301 alleles is still a controversial issue. A modifying effect of certain DRB1*04 subtypes on the susceptibility encoded by DQ alleles is possible, since not all DRB1*04-DQB1*0302 haplotypes are associated with the disease. The distribution of DRB1*04 subtypes was analysed in 240 DR4-positive Caucasian IDDM patients and 110 DR4-positive healthy controls using allele-specific hybridization after genomic amplification. Although an important contribution to IDDM predisposition was encoded by the DQB1*0302 allele which was found in the majority of patients (94.2% vs 64.7% in controls, Odd's ratio OR=8.8, P<0.0001), differences between DRB1*04 variants persisted after the effect of the DQB1 locus was removed by matching patients and controls for DQB1*0302. Thus, the DRB1*0402 allele conferred a strong IDDM-predisposing effect (OR=3.1, P<0.02) which was highly significant in the absence of DR3 on the second haplotype (OR=5.6, P<0.0001) but was not visible among DR3/4 heterozygote individuals. Conversely, the DRB1*0404 allele conferred a strong protective effect (OR=0.26, P<0.0001) which was dominant even in the presence of the associated high risk DR3 haplotype (OR=0.21, P<0.03). These data indicate that DQ molecules are not the sole contributors to the DR4-associated IDDM predisposition, and that peculiar DR4 subtypes play a significant role in susceptibility to or protection from the disease. DRB1*0402 differs from DRB1*0404 by only two acidic residues at positions 70 and 71 within the peptide binding groove, instead of amide and basic amino acids. This might induce changes of peptide binding specificity that correlate with the genetic linkage of IDDM predisposition. (C) 1996 Academic Press Limited
引用
收藏
页码:411 / 414
页数:4
相关论文
共 19 条
[1]   ASSOCIATION OF PARTICULAR HLA CLASS-II ALLELES, HAPLOTYPES AND GENOTYPES WITH SUSCEPTIBILITY TO IDDM IN THE BELGIAN POPULATION [J].
BUYSE, I ;
SANDKUYL, LA ;
GHABANBASANI, MZ ;
GU, XX ;
BOUILLON, R ;
BEX, M ;
DOOMS, L ;
EMONDS, MP ;
DUHAMEL, M ;
MARYNEN, P ;
CASSIMAN, JJ .
DIABETOLOGIA, 1994, 37 (08) :808-817
[2]   AGE-DEPENDENT HLA GENETIC-HETEROGENEITY OF TYPE-1 INSULIN-DEPENDENT DIABETES-MELLITUS [J].
CAILLATZUCMAN, S ;
GARCHON, HJ ;
TIMSIT, J ;
ASSAN, R ;
BOITARD, C ;
DJILALISAIAH, I ;
BOUGNERES, P ;
BACH, JF .
JOURNAL OF CLINICAL INVESTIGATION, 1992, 90 (06) :2242-2250
[3]   THE DISTRIBUTION OF DR4 HAPLOTYPES IN SARDINIA SUGGESTS A PRIMARY ASSOCIATION OF TYPE-I DIABETES WITH DRB1 AND DQB1 LOCI [J].
CUCCA, F ;
LAMPIS, R ;
FRAU, F ;
MACIS, D ;
ANGIUS, E ;
MASILE, P ;
CHESSA, M ;
FRONGIA, P ;
SILVETTI, M ;
CAO, A ;
DEVIRGILIIS, S ;
CONGIA, M .
HUMAN IMMUNOLOGY, 1995, 43 (04) :301-308
[4]   THE HLA-DRB1-ASTERISK-0405 HAPLOTYPE IS MOST STRONGLY ASSOCIATED WITH IDDM IN ALGERIANS [J].
DJOULAH, S ;
KHALIL, I ;
BERESSI, JP ;
BENHAMAMOUCH, S ;
BESSAOUD, K ;
DESCHAMPS, I ;
DEGOS, L ;
HORS, J .
EUROPEAN JOURNAL OF IMMUNOGENETICS, 1992, 19 (06) :381-389
[5]   HLA CLASS-II ALLELES AND SUSCEPTIBILITY AND RESISTANCE TO INSULIN-DEPENDENT DIABETES-MELLITUS IN MEXICAN-AMERICAN FAMILIES [J].
ERLICH, HA ;
ZEIDLER, A ;
CHANG, J ;
SHAW, S ;
RAFFEL, LJ ;
KLITZ, W ;
BESHKOV, Y ;
COSTIN, G ;
PRESSMAN, S ;
BUGAWAN, T ;
ROTTER, JI .
NATURE GENETICS, 1993, 3 (04) :358-364
[6]   DISTRIBUTION OF HLA-DQA1, HLA-DQB1 AND DRB1 ALLELES IN BLACK IDDM PATIENTS AND CONTROLS FROM ZIMBABWE [J].
GARCIAPACHECO, JM ;
HERBUT, B ;
CUTBUSH, S ;
HITMAN, GA ;
ZHONGLIN, W ;
MAGZOUB, M ;
BOTTAZZO, GF ;
KIERE, C ;
WEST, G ;
MVERE, D ;
BIRO, PA ;
SACHS, JA .
TISSUE ANTIGENS, 1992, 40 (03) :145-149
[7]   PEPTIDE BINDING-SPECIFICITY OF HLA-DR4 MOLECULES - CORRELATION WITH RHEUMATOID-ARTHRITIS ASSOCIATION [J].
HAMMER, J ;
GALLAZZI, F ;
BONO, E ;
KARR, RW ;
GUENOT, J ;
VALSASNINI, P ;
NAGY, ZA ;
SINIGAGLIA, F .
JOURNAL OF EXPERIMENTAL MEDICINE, 1995, 181 (05) :1847-1855
[8]  
KWOK WW, 1995, J IMMUNOL, V155, P2468
[9]   SUSCEPTIBILITY TO TYPE-1 (INSULIN-DEPENDENT) DIABETES-MELLITUS IS DETERMINED BY MHC CLASS-II MOLECULES - WHAT ABOUT DR4 [J].
MIJOVIC, CH ;
JENKINS, D ;
PENNY, MA .
DIABETOLOGIA, 1993, 36 (11) :1210-1211
[10]   ASPARTIC-ACID AT POSITION 57 OF THE HLA-DQ BETA-CHAIN PROTECTS AGAINST TYPE-I DIABETES - A FAMILY STUDY [J].
MOREL, PA ;
DORMAN, JS ;
TODD, JA ;
MCDEVITT, HO ;
TRUCCO, M .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1988, 85 (21) :8111-8115