Lefranc M P, Hammarström L, Smith C I, Lefranc G
Laboratoire d'Immunogénétique Moléculaire, URA CNRS 1191, Université Montpellier II, Sciences et Techniques du Languedoc, France.
Immunodefic Rev. 1991;2(4):265-81.
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.
在免疫球蛋白重链恒定区(Ig CH)基因中已发现单个和广泛的多基因缺失,其中一些缺失跨度达160千碱基。迄今为止,已鉴定出六种不同的多基因缺失单倍型,根据发现的时间顺序命名为I至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要么是一种缺失类型的纯合子,要么是两种不同缺失的杂合子。突尼斯人群中较高的近亲结婚率导致了这些多基因缺失纯合个体的高频率出现,这些缺失涉及Ig CH基因座中作为重组热点的高度同源区域,位于转换序列之外。在16例中的15例中,这些多基因缺失在健康人群中被观察到,尽管这些个体缺乏几种免疫球蛋白亚类,甚至一种免疫球蛋白类别。这种免疫状况使得研究这些亚类对整体免疫的重要性以及通过保留的IgG和IgA亚类分析特异性免疫反应成为可能。