Leffell Mary S, Fallin M Daniele, Hildebrand William H, Cavett Joshua W, Iglehart Brian A, Zachary Andrea A
Department of Medicine, Johns Hopkins University School of Public Health, Baltimore, MD 21205, USA.
Hum Immunol. 2004 Jan;65(1):78-89. doi: 10.1016/j.humimm.2003.10.001.
Human leukocyte antigen (HLA) class I and II alleles were defined for 302 Lakota Sioux American Indians as part of the American Society for Histocompatibility and Immunogenetics coordinated studies on minority populations. The study group was comprised of adult volunteers from the Cheyenne River and Ogala Sioux tribes residing, respectively, on the Cheyenne River and Pine Ridge Reservations in South Dakota. Of the participants, 263 (87%) claimed full American Indian ancestry through both maternal and paternal grandparents. The study group included 25 nuclear families that were informative for genotyping. HLA phenotypes from 202 adults with no other known first-degree relative included in the study were used for calculation of allele and haplotype frequencies by maximum likelihood estimation. HLA-A, -B, and -Cw alleles were found to be in Hardy Weinberg equilibrium. Deviation from equilibrium was observed for DRB1 alleles (p=0.01), but could be attributed to the sample size and the occurrence of some genotypes with low expected frequencies. Polymorphism among the Sioux was limited with four to seven alleles comprising >80% of those observed at each locus. Several alleles were found at high frequency (0.05-0.30) among the Sioux that are also prevalent in other Native Americans and Alaska Natives, including: A2402, 3101, and 0206; B3501,3901, 5101, and 2705; Cw0702, 0404, and 03041; DRB10407, 0404, 1402, and 16021; and DQB10301, 0302, and 0402. DRB10811, which has been only previously described in Navajo and Tlingit Indians, was found to occur at a frequency of 0.119 among the Sioux. Two new alleles were defined among the Sioux: Cw0204 and DRB1040703, which were found in two and four individuals, respectively. In the haplotype analyses, significant linkage disequilibrium (p<0.00001) was seen in all pairwise comparisons of loci and numerous two and three locus haplotypes were found to have strong, positive linkage disequilibrium values. The two most common extended haplotypes among the Sioux, determined by maximum likelihood estimation and genotyping were: A31012, B3501, Cw0404, DRB10407; and A24021, B3501, Cw0404, DRB10404.
作为美国组织相容性与免疫遗传学协会针对少数族裔人群开展的协作研究的一部分,对302名拉科塔苏族美国印第安人进行了人类白细胞抗原(HLA)I类和II类等位基因分型。研究组由分别居住在南达科他州夏延河保留地和派恩岭保留地的夏延河苏族部落和奥格拉拉苏族部落的成年志愿者组成。在参与者中,263人(87%)称其父母双方的祖父母均为纯正的美国印第安血统。研究组包括25个对基因分型有参考价值的核心家庭。研究中纳入的202名无其他已知一级亲属的成年人的HLA表型,用于通过最大似然估计来计算等位基因和单倍型频率。发现HLA - A、- B和 - Cw等位基因处于哈迪 - 温伯格平衡。观察到DRB1等位基因偏离平衡状态(p = 0.01),但这可能归因于样本量以及一些预期频率较低的基因型的出现。苏族人中的多态性有限,每个位点观察到的等位基因中有4至7个占比超过80%。在苏族人中发现了几个高频(0.05 - 0.30)等位基因,这些等位基因在其他美洲原住民和阿拉斯加原住民中也很常见,包括:A2402、3101和0206;B3501、3901、5101和2705;Cw0702、0404和03041;DRB10407、0404、1402和16021;以及DQB10301、0302和0402。DRB10811此前仅在纳瓦霍族和特林吉特族印第安人中被描述过,在苏族人中的出现频率为0.119。在苏族人中定义了两个新等位基因:Cw0204和DRB1040703,分别在两人和四人中发现。在单倍型分析中,所有位点的两两比较均出现显著的连锁不平衡(p < 0.00001),并且发现许多两个和三个位点的单倍型具有很强的正连锁不平衡值。通过最大似然估计和基因分型确定的苏族人中两个最常见的扩展单倍型为:A31012、B3501、Cw0404、DRB10407;以及A24021、B3501、Cw0404、DRB10404。