人免疫球蛋白重链恒定区基因缺失:分子和免疫学分析。

Immunodeficiency reviews Pub Date : 1991-01-01
M P Lefranc, L Hammarström, C I Smith, G Lefranc
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引用次数: 0

摘要

在Ig CH免疫球蛋白重链恒定区基因中描述了单基因和广泛的多基因缺失,其中一些包含高达160千碱基。迄今为止,已经确定了六种不同的多基因缺失单倍型,根据其发现的时间顺序命名为I到VI;缺失I (del G1-EP1-A1-GP-G2- g4)、II (del EP1-A1-GP)、III (del A1-GP-G2-G4-E)、IV (del EP1-A1-GP- g2 - g4)、V (del GP-G2-G4-E-A2)、VI (del G1-EP1-A1-GP-G2)。主要在地中海地区发现个体或纯合一种缺失或杂合两种不同的缺失。突尼斯人群中高水平的血缘关系解释了这些多基因缺失中一个或另一个纯合的个体的高频率,这些缺失涉及作为重组热点的高度同源区域,在开关序列之外,在Ig CH位点。在16例中,有15例在健康人群中观察到这些多基因缺失,尽管这些个体缺乏几种免疫球蛋白亚类,甚至只有一类。这样的免疫学情况使得研究这些亚类对整体免疫的重要性,并分析保留的IgG和IgA亚类的特异性免疫反应成为可能。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Gene deletions in the human immunoglobulin heavy chain constant region locus: molecular and immunological analysis.

Single and extensive multigene deletions have been described in the Ig CH immunoglobulin heavy-chain constant region genes, some of these encompassing up to 160 kilobases. To date six different multigene deletion haplotypes have been identified, designated I to VI according to the chronological order of their findings; deletion I (del G1-EP1-A1-GP-G2-G4), II (del EP1-A1-GP), III (del A1-GP-G2-G4-E), IV (del EP1-A1-GP-G2-G4), V (del GP-G2-G4-E-A2), VI (del G1-EP1-A1-GP-G2). Individuals were found either homozygous for one type of deletion or heterozygous for two different deletions, mainly in the Mediterranean area. The high level of consanguinity in the Tunisian population accounts for the high frequency of individuals homozygous for one or the other of these multigene deletions which involve highly homologous regions as hot spots of recombinations, outside of the switch sequences, in the Ig CH locus. In 15 cases out of 16, these multigene deletions have been observed in healthy people, although these individuals lacked several immunoglobulin subclasses and, even, one class. Such an immunological situation makes it possible to study the importance of these subclasses for the overall immunity, and to analyse the specific immune responses by the retained IgG and IgA subclasses.

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