Démant P, Iványi D, Oudshoorn-Snoek M, Calafat J, Roos M H
Immunol Rev. 1981;60:5-22. doi: 10.1111/j.1600-065x.1981.tb00360.x.
Since the discovery of the H-2Ld molecule (Lemonnier et al. 1975) we have demonstrated that several K and D region alleles produce more than one type of H-2 molecules. Two of four different molecules were distinguished in the products of different alleles. Some of these molecules are products of different genes (H-2D, H-2L), in other instances the evidence for distinct genes is not available. Some of the different molecules produced by the same region might be modified products of the same gene. In the instances where no information implicating different genes is available, we use a neutral terminology which does not presume a genetic difference: H-2K1d and H-2K2d, H-2D1k, H-2D2k, H-2D1dx, H-2D2dx, H-2L1d, H-2L2d, etc. Immunoprecipitation experiments with some anti-H-2L and anti-Qa-2 sera revealed proteins with the apparent molecular weight of 41,000. We designate these antigens provisionally Lq and Qx, respectively. The Lq protein is polymorphic and it is at least partly under the control of H-2L-linked genes since it is absent from BALB/c-H-2dm2 cells. Since we have never seen the 41,000 proteins in precipitates of H-2K or H-2D antigens, it appears that whatever the origin of these molecules, they reveal some features common to products of L and Qa region. The basic relationship of H-2 K, D, L antigens is revealed also by the shared antigenic specificities between these H-2 molecules which we demonstrate using anti-H-2.28 sera. In summary, our results show that the class I antigens in each haplotype represent a family of several distinct but antigenically related molecules. The specificities of the H-2.28 family are the strongest allotype common to different H-2 K, D, and L molecules. Recent direct demonstration of several different genes in the Dd region (Steinmetz et al. 1981) provides evidence for the genetic complexity of H-2 genes which may be underlying basis of the molecular heterogeneity of H-2 antigens discussed here.
自从发现H-2Ld分子(Lemonnier等人,1975年)以来,我们已经证明,几个K和D区域的等位基因会产生不止一种类型的H-2分子。在不同等位基因的产物中,区分出了四种不同分子中的两种。其中一些分子是不同基因(H-2D、H-2L)的产物,在其他情况下,尚无明确基因的证据。同一区域产生的一些不同分子可能是同一基因的修饰产物。在没有涉及不同基因信息的情况下,我们使用中性术语,不假定存在遗传差异:H-2K1d和H-2K2d、H-2D1k、H-2D2k、H-2D1dx、H-2D2dx、H-2L1d、H-2L2d等。用一些抗H-2L和抗Qa-2血清进行的免疫沉淀实验显示出表观分子量为41,000的蛋白质。我们分别将这些抗原暂时命名为Lq和Qx。Lq蛋白具有多态性,并且至少部分受H-2L连锁基因的控制,因为在BALB/c-H-2dm2细胞中不存在该蛋白。由于我们从未在H-2K或H-2D抗原的沉淀物中看到过41,000的蛋白质,所以无论这些分子的来源如何,它们似乎都揭示了L和Qa区域产物共有的一些特征。我们使用抗H-2.28血清证明,这些H-2分子之间的共同抗原特异性也揭示了H-2 K、D、L抗原的基本关系。总之,我们的结果表明,每个单倍型中的I类抗原代表了几个不同但抗原相关的分子家族。H-2.28家族的特异性是不同H-2 K、D和L分子共有的最强同种异型。最近在Dd区域直接证明了几个不同的基因(Steinmetz等人,1981年),这为H-2基因的遗传复杂性提供了证据,这可能是这里讨论的H-2抗原分子异质性的潜在基础。