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人类主要组织相容性复合体II类分子作为分化标志物。

Human MHC class II molecules as differentiation markers.

作者信息

van Heyningen V, Guy K, Newman R, Steel C M

出版信息

Immunogenetics. 1982;16(5):459-69. doi: 10.1007/BF00372104.

Abstract

DA6.231 and DA6.164 are mouse monoclonal antibodies that immunoprecipitate HLA-DR-like p34,29 glycoprotein dimers from surface- and metabolically-labeled cells. On lymphoblastoid cell lines the distribution of the 231 epitope is completely nonpolymorphic, while the 164 epitope is present on all cells except on those that are DR7 homozygous. Binding-inhibition studies show that the 231 and 164 epitopes are spatially close to each other when present on the same molecule. The mutual inhibition pattern and the absence of the 164 epitope from the 231+ cells of a few leukemia patients suggest, however, that 231 and 164 epitopes are not invariably present together. Most DR-positive cells possess 231+ and 164+ and 231+ 164- class II molecules in approximately a 2:1 ratio. This has been confirmed by immune depletion studies. Thus DA6.231 appears to define a supralocus epitope. The 164 epitope may be a marker for a subset of class II molecules exhibiting differential expression on various cell types immortalized by malignant transformation.

摘要

DA6.231和DA6.164是小鼠单克隆抗体,可从经表面标记和代谢标记的细胞中免疫沉淀出HLA - DR样p34,29糖蛋白二聚体。在淋巴母细胞系上,231表位的分布完全无多态性,而164表位存在于所有细胞上,除了那些DR7纯合的细胞。结合抑制研究表明,当231和164表位存在于同一分子上时,它们在空间上彼此靠近。然而,少数白血病患者的231 +细胞中164表位的相互抑制模式和缺失表明,231和164表位并非总是同时存在。大多数DR阳性细胞拥有231 +和164 +以及231 + 164 - II类分子,比例约为2:1。这已通过免疫耗竭研究得到证实。因此,DA6.231似乎定义了一个超基因座表位。164表位可能是II类分子亚群的一个标记,该亚群在通过恶性转化永生化的各种细胞类型上表现出差异表达。

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