HLA-DP POLYMORPHISM IN SUDANESE CONTROLS AND PATIENTS WITH INSULIN-DEPENDENT DIABETES-MELLITUS
被引:23
作者:
MAGZOUB, MMA
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机构:UNIV LONDON LONDON HOSP,COLL MED,DEPT IMMUNOL,TURNER ST,LONDON E1 2AD,ENGLAND
MAGZOUB, MMA
STEPHENS, HAF
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机构:UNIV LONDON LONDON HOSP,COLL MED,DEPT IMMUNOL,TURNER ST,LONDON E1 2AD,ENGLAND
STEPHENS, HAF
SACHS, JA
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机构:UNIV LONDON LONDON HOSP,COLL MED,DEPT IMMUNOL,TURNER ST,LONDON E1 2AD,ENGLAND
SACHS, JA
BIRO, PA
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机构:UNIV LONDON LONDON HOSP,COLL MED,DEPT IMMUNOL,TURNER ST,LONDON E1 2AD,ENGLAND
BIRO, PA
CUTBUSH, S
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机构:UNIV LONDON LONDON HOSP,COLL MED,DEPT IMMUNOL,TURNER ST,LONDON E1 2AD,ENGLAND
CUTBUSH, S
WU, Z
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机构:UNIV LONDON LONDON HOSP,COLL MED,DEPT IMMUNOL,TURNER ST,LONDON E1 2AD,ENGLAND
WU, Z
BOTTAZZO, GF
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机构:UNIV LONDON LONDON HOSP,COLL MED,DEPT IMMUNOL,TURNER ST,LONDON E1 2AD,ENGLAND
BOTTAZZO, GF
机构:
[1] UNIV LONDON LONDON HOSP,COLL MED,DEPT IMMUNOL,TURNER ST,LONDON E1 2AD,ENGLAND
[2] UNIV GEZIRA,FAC MED,KHARTOUM,SUDAN
[3] ARMED FORCES RES INST MED SCI,DEPT IMMUNOL,BANGKOK,THAILAND
来源:
TISSUE ANTIGENS
|
1992年
/
40卷
/
02期
关键词:
HLA-DP POLYMORPHISM;
IDDM;
SUDANESE;
OLIGOTYPING;
D O I:
10.1111/j.1399-0039.1992.tb01961.x
中图分类号:
Q2 [细胞生物学];
学科分类号:
071009 ;
090102 ;
摘要:
Human leukocyte antigen (HLA) genes are candidates for susceptibility to insulin-dependent diabetes mellitus (IDDM). The association of IDDM with particular DR and DQ alleles has been reported in all populations studied, but its association with HLA-DP alleles has been controversial. To address this question we analyzed 19 DPB1 and 2 DPA1 alleles and their associations in well-characterized Sudanese (an admixture of Arab and Black) IDDM patients (n = 71) and ethnically matched controls (n = 86) using polymerase chain reaction-sequence specific oligonucleotide (PCR-SSO) typing. There were no significant differences between the patient and control groups in the DPB1 frequencies. DPB1*0201, *0401 and DPA1*01 were the most frequent alleles in both IDDM patients and control subjects. Significant positive and negative associations between DPB1 and DPA1 alleles were detected in both groups. A novel DPB1 allele included in DPB1*1701 was identified.