HLA class II disease associations in southern Africa

被引:39
作者
Lombard, Z
Brune, AE
Hoal, EG
Babb, C
Van Helden, PD
Epplen, JT
Bornman, L
机构
[1] Univ Stellenbosch, Dept Med Biochem, Fac Hlth Sci, MRC,Ctr Mol & Cellular Biol, ZA-7505 Tygerberg, South Africa
[2] Univ Johannesburg, Dept Biochem, ZA-2006 Auckland Pk, South Africa
[3] Ruhr Univ Bochum, Dept Human Genet, D-44780 Bochum, Germany
来源
TISSUE ANTIGENS | 2006年 / 67卷 / 02期
关键词
disease association; HLA class II; resistance; southern Africa; susceptibility;
D O I
10.1111/j.1399-0039.2006.00530.x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Southern Africa harbors several population groups representing a diversity of gene pool origins. This provides a unique opportunity to study genetic disease predisposition in these populations against a common environmental background. Human leukocyte antigen (HLA) association studies of these populations could improve knowledge on inter-population variation and HLA-related disease susceptibility. The aim of this paper is to review HLA class 11 disease associations reported for southern African population groups, compare them with findings in other populations and identify those unique to southern Africa. A number of HLA class 11 disease associations appear to be unique to southern African populations. These include DRB1*14011 association with insulin-dependent diabetes mellitus susceptibility in the Xhosa and DRB1*10 and DQB1*0302 with rheumatoid arthritis susceptibility in the South African (SA) Indian and SA Coloreds, respectively. A noteworthy similarity in class 11 disease association was observed among southern African Caucasoid and their European parental populations. Unique HLA class 11 disease associations observed in southern Africa are consistent with the notion that unique environmental and natural selective factors have resulted in certain ethnic-specific HLA class 11 disease associations, while common HLA class 11 disease associations found across different populations support the notion that common diseases are caused by common, ancient alleles present in indigenous African populations.
引用
收藏
页码:97 / 110
页数:14
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