Stohl W, Kunkel H G
Scand J Immunol. 1984 Sep;20(3):273-8. doi: 10.1111/j.1365-3083.1984.tb01003.x.
The T-cell differentiation antigen T4/Leu3 has been described as a non-polymorphic molecule important in T-cell recognition of class II major histocompatibility complex antigens. We report the polymorphism of this molecule in black individuals as manifest by a heterogeneity of staining with OKT4 monoclonal antibody. No such heterogeneity was observed when staining with other monoclonal antibodies that bind to different epitopes of the same molecule. No heterogeneity of staining with any of the monoclonal antibodies was observed in whites. Three patterns of OKT4 staining emerged: intact, deficient, and intermediate. This heterogeneity is likely to be due to an intrinsic heterogeneity in T4 epitope expression and not secondary to an interfering plasma factor as shown by the preservation of the T4 epitope pattern after a 3-day culture in the presence or absence of mitogen. Family studies strongly suggest that this heterogeneity in T4 epitope expression is inherited in an autosomal codominant fashion.
T细胞分化抗原T4/Leu3被描述为一种在T细胞识别II类主要组织相容性复合体抗原中起重要作用的非多态性分子。我们报告了该分子在黑人个体中的多态性,表现为用OKT4单克隆抗体染色时的异质性。当用与同一分子不同表位结合的其他单克隆抗体染色时,未观察到这种异质性。在白人中,用任何一种单克隆抗体染色均未观察到异质性。出现了三种OKT4染色模式:完整型、缺陷型和中间型。这种异质性可能是由于T4表位表达的内在异质性,而不是继发于干扰性血浆因子,这在有丝分裂原存在或不存在的情况下进行3天培养后T4表位模式的保留中得到了证明。家系研究强烈表明,T4表位表达的这种异质性是以常染色体共显性方式遗传的。