HLA antigens, Alleles and Haplotypes among the Yup'ik Alaska natives: Report of the ASHI minority workshops, part II

被引:43
作者
Leffell, MS
Fallin, MD
Erlich, HA
Fernandez-Vina, M
Hildebrand, WH
Mack, SJ
Zachary, AA
机构
[1] Johns Hopkins Univ, Sch Med, Immunogenet Lab, Dept Med, Baltimore, MD 21205 USA
[2] Johns Hopkins Univ, Sch Publ Hlth, Dept Epidemiol, Baltimore, MD 21205 USA
[3] Georgetown Univ, CW Bill Young DoD Marrow Program, Kensingtown, MD USA
[4] Univ Oklahoma, Oklahoma City, OK USA
[5] Roche Mol Syst, Dept Human Genet, Alameda, CA USA
[6] Childrens Hosp, Oakland Res Inst, Oakland, CA 94609 USA
关键词
Yup'ik Eskimo; Alaska native; HLA alleles; HLA haplotypes;
D O I
10.1016/S0198-8859(02)00415-9
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
As part of the American Society for Histocompatibility and Immunogenetics coordinated studies among minority populations, human leukocyte antigen (FILA) alleles were defined for 460 Volunteer Yup'ik Eskimos from the Yukon Kuskokwim delta region of south-western Alaska. The study group included 252 adults with no other first-degree relatives and 48 informative nuclear families. Full Yupik ancestry through both maternal and paternal grandparents wits claimed by 81.1% of participants. HLA-A, -B, -Cw, -DRB1, and -DQB1 alleles were determined by SBT, SSOP, reverse SSOP, and/or RSCA according to the protocols of five participating laboratories. Polymorphism was limited with 3-6 alleles comprising > 80% of the alleles observed at each locus. Homozygosity was high, particularly at the HLA-A and -DQB1 loci, with 36.6% and 14% of individuals having a single allele defined at these respective loci. HLA-A, -B, and -DRB1 alleles were in Hardy-Weinberg equilibrium, whereas HLA-Cw and -DQB1 alleles gave significant deviation (p = 0.002; 0.005). Significant linkage disequilibrium (p less than or equal to 0.00001) was observed in all pairwise evaluations. A new Cw*0806 allele was observed in high linkage disequilibrium with B*4801 (Delta = 0.099; Delta(rcl) = 1.0). Three extended haplotypes were found to have frequencies > 5%, the most prevalent being A*2402; B*4801; DRB1*0401; DQB1*0301 (0.0933). Comparison of available class I data indicate that the Yup'ik share several common alleles with other Native American populations, including: A*2402,.0206, *6801; B*1501, *2705, *3501, *4002, *4801, *5101; and Cw*0202, *0304, *0401. Comparisons of class II data also confirm a close relationship of the Yup'ik to two other Eskimo Populations, Siberian and East Greenland Eskimos. DRB1*0401 and *1101, Which Occur in high frequency among these Eskimo populations, but not in other Native Americans, were also prevalent among the Yup'ik, with respective frequencies of 0.232 and 0.107. (C) American Society for Histocompatibility and Immunogenetics, 2002. Published by Elsevier Science Inc.
引用
收藏
页码:614 / 625
页数:12
相关论文
共 25 条
[1]   HLA-A2 SUBTYPES ARE FUNCTIONALLY DISTINCT IN PEPTIDE BINDING AND PRESENTATION [J].
BAROUCH, D ;
FRIEDE, T ;
STEVANOVIC, S ;
TUSSEY, L ;
SMITH, K ;
ROWLANDJONES, S ;
BRAUD, V ;
MCMICHAEL, A ;
RAMMENSEE, HG .
JOURNAL OF EXPERIMENTAL MEDICINE, 1995, 182 (06) :1847-1856
[2]  
BEEMAN S, 2001, ALASKA GEOGRAPHIC, V28, P4
[3]   Nomenclature for factors of the HLA system, 1996 [J].
Bodmer, JG ;
Marsh, SGE ;
Albert, ED ;
Bodmer, WF ;
Bontrop, RE ;
Charron, D ;
Dupont, B ;
Erlich, HA ;
Fauchet, R ;
Mach, B ;
Mayr, WR ;
Parham, P ;
Sasazuki, T ;
Schreuder, GMT ;
Strominger, JL ;
Svejgaard, A ;
Terasaki, PI .
HUMAN IMMUNOLOGY, 1997, 53 (01) :98-128
[4]   Nomenclature for factors of the HLA system, 1998 [J].
Bodmer, JG ;
Marsh, SGE ;
Albert, ED ;
Bodmer, WF ;
Bontrop, RE ;
Dupont, B ;
Erlich, HA ;
Hansen, JA ;
Mach, B ;
Mayr, WR ;
Parham, P ;
Petersdorf, EW ;
Sasazuki, T ;
Schreuder, GMT ;
Strominger, JL ;
Svejgaard, A ;
Terasaki, PI .
TISSUE ANTIGENS, 1999, 53 (04) :407-446
[5]  
BOYER GS, 1994, J RHEUMATOL, V21, P2292
[6]   Analysis of the frequencies of HLA-A, B, and C alleles and haplotypes in the five major ethnic groups of the United States reveals high levels of diversity in these loci and contrasting distribution patterns in these populations [J].
Cao, K ;
Hollenbach, J ;
Shi, XJ ;
Shi, WX ;
Chopek, M ;
Fernández-Viña, MA .
HUMAN IMMUNOLOGY, 2001, 62 (09) :1009-1030
[7]   Hardy-Weinberg testing for HLA class II (DRB1, DQA1, DQB1, AND DPB1) loci in 26 human ethnic groups [J].
Chen, JJ ;
Hollenbach, JA ;
Trachtenberg, EA ;
Just, JJ ;
Carrington, M ;
Ronningen, KS ;
Begovich, A ;
King, MC ;
McWeeney, S ;
Mack, SJ ;
Erlich, HA ;
Thomson, G .
TISSUE ANTIGENS, 1999, 54 (06) :533-542
[8]   Sequence-based typing of HLA class I alleles in Alaskan Yupik Eskimo [J].
Ellexson-Turner, ME ;
Leffell, MS ;
Zachary, AA ;
Turner, S ;
Bennett, T ;
Sidebottom, DA ;
Cao, K ;
Fernández-Viña, M ;
Hildebrand, WH .
HUMAN IMMUNOLOGY, 2001, 62 (06) :639-644
[9]   Frequencies of HLA-A2 alleles in five US population groups - Predominance of A*02011 and identification of HLA-A*0231 [J].
Ellis, JM ;
Henson, V ;
Slack, R ;
Ng, J ;
Hartzman, RJ ;
Hurley, CK .
HUMAN IMMUNOLOGY, 2000, 61 (03) :334-340
[10]   HLA class II alleles in Amerindian populations: Implications for the evolution of HLA polymorphism and the colonization of the Americas [J].
Erlich, HA ;
Mack, SJ ;
Bergstrom, T ;
Gyllensten, UB .
HEREDITAS, 1997, 127 (1-2) :19-24