Caucasian Origin of Disease Associated HLA Haplotypes in Chinese Blood Donors with IgA Deficiency

被引:12
作者
Wang, Ning [1 ]
Lu, Ping [2 ]
Ling, Bing [2 ]
Zhu, Ziyan [2 ]
Hammarstrom, Lennart [1 ]
机构
[1] Karolinska Univ, Huddinge Hosp, Karolinska Inst, Dept Lab Med,Div Clin Immunol F79, SE-14186 Stockholm, Sweden
[2] Shanghai Blood Ctr, Shanghai Inst Blood Transfus, Shanghai 200051, Peoples R China
基金
瑞典研究理事会;
关键词
IgA deficiency; genetics; human leukocyte antigen (HLA); Chinese; SYSTEMIC-LUPUS-ERYTHEMATOSUS; MAJOR HISTOCOMPATIBILITY COMPLEX; PRIMARY IMMUNODEFICIENCIES; RHEUMATOID-ARTHRITIS; ALLELIC ASSOCIATIONS; JAPANESE POPULATION; MOLECULAR ANALYSIS; ASIAN POPULATIONS; GRAVES-DISEASE; SUSCEPTIBILITY;
D O I
10.1007/s10875-013-9983-1
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Purpose Selective immunoglobulin A deficiency (IgAD) is the most common primary immunodeficiency in Caucasians with a prevalence of 1:600. However, the prevalence of IgAD is markedly lower in East Asian countries but no genetic studies have been performed on IgAD individuals in the Mongoloid population. Methods We investigated the prevalence of IgAD in a large number of Chinese blood donors (n= 39,015) in Shanghai, China. We measured immunoglobulin class, IgG subclass and anti-IgA serum levels among the IgAD donors. These donors were subsequently tissue typed and the allele frequency was compared with the Shanghai bone marrow donor HLA registry. Results Seventeen IgAD Chinese blood donors were identified, giving a prevalence of 1:2,295. Two previously identified IgAD blood donor samples were added in the subsequent tests. Most IgAD donors had serum IgG levels above the normal range with no major IgG subclass deficiency and one donor was weakly positive for anti-IgA. Two-thirds of the Chinese IgAD donors carried Caucasian IgAD associated risk haplotypes, including DRB1*0301-DQB1*0201, DRB1*0701-DQB1*0202 and DRB1*0102-DQB1*0501, giving a significantly higher frequency of these haplotypes as compared to the Shanghai bone marrow donor HLA registry. Conclusions The prevalence of IgAD in Chinese in this study is markedly lower than in Caucasians. This is the first study to investigate the genetics of IgAD in the Mongoloid population and two-thirds of the Chinese IgAD donors showed a mixture of Caucasian IgAD risk haplotypes. The low prevalence of IgAD could potentially be due to the low frequency of the disease associated risk haplotypes in China.
引用
收藏
页码:157 / 162
页数:6
相关论文
共 49 条
  • [1] IMMUNOLOGICAL ASPECTS OF EPILEPSY
    AARLI, JA
    [J]. BRAIN & DEVELOPMENT, 1993, 15 (01) : 41 - 50
  • [2] HLA AND SYSTEMIC LUPUS-ERYTHEMATOSUS IN CHINESE
    CHAN, SH
    FENG, PH
    SRINIVASAN, N
    WEE, GB
    CHAN, HC
    [J]. HUMAN IMMUNOLOGY, 1981, 3 (04) : 345 - 350
  • [3] RECURRENT EXTENDED HLA HAPLOTYPES IN CHILDREN WITH SELECTIVE IGA DEFICIENCY
    CUCCIABELVEDERE, M
    MONAFO, V
    MARTINETTI, M
    PLEBANI, A
    DEPAOLI, F
    BURGIO, GR
    [J]. TISSUE ANTIGENS, 1989, 34 (02): : 127 - 132
  • [4] SELECTIVE IGA DEFICIENCY, IGG SUBCLASS DEFICIENCY, AND THE MAJOR HISTOCOMPATIBILITY COMPLEX
    CUNNINGHAMRUNDLES, C
    FOTINO, M
    ROSINA, O
    PETER, JB
    [J]. CLINICAL IMMUNOLOGY AND IMMUNOPATHOLOGY, 1991, 61 (02): : S61 - S69
  • [5] HLA-A, -B, -DR haplotype frequencies from DNA typing data of 26,266 Chinese bone marrow donors
    Du, Ke-Ming
    Ji, Yun
    Xie, Jun-Hua
    Fu, Min
    Sun, Ying
    Jin, Ye
    Sun, Ji-Li
    Yang, Jian-Hao
    Zhang, Zheng
    Mao, Zhen
    Liu, Da-Zhuang
    Qian, Kai-Cheng
    Zhao, Tong-Mao
    [J]. HUMAN IMMUNOLOGY, 2007, 68 (10) : 854 - 866
  • [6] Feng L, 1992, Zhonghua Yi Xue Za Zhi, V72, P88
  • [7] Prevalence of immunoglobulin A deficiency in Chinese blood donors and evaluation of anaphylactic transfusion reaction risk
    Feng, M. L.
    Zhao, Y. L.
    Shen, T.
    Huang, H.
    Yin, B.
    Liu, R. Z.
    Qian, K. C.
    Liu, D-Z.
    [J]. TRANSFUSION MEDICINE, 2011, 21 (05) : 338 - 343
  • [8] High-Density SNP Mapping of the HLA Region Identifies Multiple Independent Susceptibility Loci Associated with Selective IgA Deficiency
    Ferreira, Ricardo C.
    Pan-Hammarstrom, Qiang
    Graham, Robert R.
    Fontan, Gumersindo
    Lee, Annette T.
    Ortmann, Ward
    Wang, Ning
    Urcelay, Elena
    Fernandez-Arquero, Miguel
    Nunez, Concepcion
    Jorgensen, Gudmundur
    Ludviksson, Bjorn R.
    Koskinen, Sinikka
    Haimila, Katri
    Padyukov, Leonid
    Gregersen, Peter K.
    Hammarstrom, Lennart
    Behrens, Timothy W.
    [J]. PLOS GENETICS, 2012, 8 (01)
  • [9] Association of IFIH1 and other autoimmunity risk alleles with selective IgA deficiency
    Ferreira, Ricardo C.
    Pan-Hammarstrom, Qiang
    Graham, Robert R.
    Gateva, Vesela
    Fontan, Gumersindo
    Lee, Annette T.
    Ortmann, Ward
    Urcelay, Elena
    Fernandez-Arquero, Miguel
    Nunez, Concepcion
    Jorgensen, Gudmundur
    Ludviksson, Bjorn R.
    Koskinen, Sinikka
    Haimila, Katri
    Clark, Hilary F.
    Klareskog, Lars
    Gregersen, Peter K.
    Behrens, Timothy W.
    Hammarstrom, Lennart
    [J]. NATURE GENETICS, 2010, 42 (09) : 777 - U69
  • [10] Discordant association of islet autoantibodies with high-risk HLA genes in Chinese type 1 diabetes
    Gu, Yong
    Zhang, Mei
    Chen, Heng
    Wang, Zhixiao
    Xing, Chunyan
    Yang, Hui
    Xu, Xinyu
    Liu, Yu
    Zhou, Zhiguang
    Yu, Liping
    Hutton, John
    Eisenbarth, George
    Yang, Tao
    [J]. DIABETES-METABOLISM RESEARCH AND REVIEWS, 2011, 27 (08) : 899 - 905