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利用单克隆抗体对DRw6相关表位进行生化剖析。

Biochemical dissection of DRw6 related epitopes using monoclonal antibodies.

作者信息

Johnson J P, Wank R

出版信息

Hum Immunol. 1986 May;16(1):69-80. doi: 10.1016/0198-8859(86)90036-4.

Abstract

Three monoclonal antibodies (MoAbs) directed against polymorphic epitopes of Ia antigens were used as tools for a serological and biochemical dissection of the class II products encoded by the HLA-DRw6 haplotype. MoAb 16.23 defines an epitope common to DRw13 and DR3 haplotypes, MoAb S5 defines an epitope common to DRw13 and DR2 haplotypes, and MoAb S2 defines an epitope apparently restricted to DRw13. Not all DRw13 cells express these epitopes. Analysis of 16 DRw6 homozygous typing cells showed that expression of all three epitopes was restricted to those DRw13 cells that carried the Dw18 antigen, the DRw13 Dw19 cells being negative. The relationships among the molecules bearing these epitopes were investigated using sequential immunoprecipitation in lymphoblastoid cell lines derived from genetically characterized individuals. In both DRw13 and DR2 bearing cells, the DR2 + w13 epitope was localized to a population of DQ molecules which also carried the DQw1 specificity defined by MoAb Genox 3.53. The S5 epitope is therefore a private specificity that distinguishes the DQw1 antigens encoded by the DR2 and DRw13 haplotypes from the DQw1 antigens encoded by other haplotypes. The DRw13 and the DR3 + w13 epitopes were both shown to be expressed on DR molecules that also carried a DRw52-like specificity. In a DRw13 haplotype encoding both the S2 and 16.23 epitopes, the epitopes appeared to be located on separate molecules. The antibodies described here can distinguish between DRw13 cells which carry different Dw antigens, identify a private specificity on the DQw1 antigen, and define two distinct DR molecules encoded by some DRw13 haplotypes.

摘要

三种针对Ia抗原多态性表位的单克隆抗体(MoAb)被用作工具,对由HLA - DRw6单倍型编码的II类产物进行血清学和生化分析。单克隆抗体16.23确定了DRw13和DR3单倍型共有的一个表位,单克隆抗体S5确定了DRw13和DR2单倍型共有的一个表位,单克隆抗体S2确定了一个显然仅限于DRw13的表位。并非所有DRw13细胞都表达这些表位。对16个DRw6纯合定型细胞的分析表明,所有这三种表位的表达都仅限于那些携带Dw18抗原的DRw13细胞,DRw13 Dw19细胞为阴性。利用来自基因特征明确个体的淋巴母细胞系中的连续免疫沉淀法,研究了携带这些表位的分子之间的关系。在携带DRw13和DR2的细胞中,DR2 + w13表位定位于一群DQ分子,这些分子也携带由单克隆抗体Genox 3.53确定的DQw1特异性。因此,S5表位是一种独特的特异性,它将由DR2和DRw13单倍型编码的DQw1抗原与由其他单倍型编码的DQw1抗原区分开来。DRw13和DR3 + w13表位都显示在也携带DRw52样特异性的DR分子上表达。在一个编码S2和16.23表位的DRw13单倍型中,这些表位似乎位于不同的分子上。本文所述的抗体可以区分携带不同Dw抗原的DRw13细胞,识别DQw1抗原上的独特特异性,并确定由某些DRw13单倍型编码的两种不同的DR分子。

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