Oriol R, Le Pendu J, Mollicone R
Vox Sang. 1986;51(3):161-71. doi: 10.1111/j.1423-0410.1986.tb01946.x.
The present knowledge on chemical, enzymatic, serologic and genetic aspects of ABH antigens is reviewed in an effort to produce a simple and coherent genetic model for the biosynthesis of these antigens and chemically related structures. The genetic control of type 1 (Le(a), Le(b), Le(c) and Le(d)), type 2 (X, Y, I, and H), type 3 and type 4 ABH and related antigens in different animal and human tissues is analyzed, taking into account the properties of the glycosyltransferases which are involved in their synthesis and considering possible competition for common acceptor and donor substrates. The phylogeny of ABH determinants shows that they appeared as tissular antigens much earlier than as red cell antigens. The ontogeny of ABH antigens suggests that they behave as differentiation antigens, and an effort is made to correlate their tissular distribution in the adult with the embryological origin of each tissue.
本文回顾了目前关于ABH抗原的化学、酶学、血清学和遗传学方面的知识,旨在建立一个简单且连贯的遗传模型,用于这些抗原及化学相关结构的生物合成。分析了不同动物和人体组织中1型(Le(a)、Le(b)、Le(c)和Le(d))、2型(X、Y、I和H)、3型和4型ABH及相关抗原的遗传控制,同时考虑了参与其合成的糖基转移酶的特性,并探讨了共同受体和供体底物可能存在的竞争情况。ABH决定簇的系统发育表明,它们作为组织抗原出现的时间比作为红细胞抗原出现的时间要早得多。ABH抗原的个体发生表明它们表现为分化抗原,本文还努力将其在成体中的组织分布与各组织的胚胎起源联系起来。