Bay S, Lo-Man R, Osinaga E, Nakada H, Leclerc C, Cantacuzène D
Unité de Chimie Organique, Institut Pasteur, Paris, France.
J Pept Res. 1997 Jun;49(6):620-5. doi: 10.1111/j.1399-3011.1997.tb01171.x.
The glycosidic tumor-associated Tn antigen was conjugated to a lysine backbone containing a helper T-cell epitope in order to activate immune responses specific for some types of carcinomas. As opposed to traditional protein conjugates, this multiple antigen glycopeptide (MAG) offers the advantages of the lack of immunogenicity of the polylysine core and of accurate chemical definition. The MAG construction was assembled by conventional solid-phase peptide synthesis. The analysis of its antigenicity demonstrated that the Tn antigen on the MAG is recognized by Tn-specific monoclonal antibodies.
将糖苷化肿瘤相关Tn抗原与含有辅助性T细胞表位的赖氨酸主链偶联,以激活针对某些类型癌症的特异性免疫反应。与传统的蛋白质偶联物不同,这种多抗原糖肽(MAG)具有聚赖氨酸核心缺乏免疫原性和精确化学定义的优点。MAG构建体通过传统的固相肽合成组装而成。其抗原性分析表明,MAG上的Tn抗原可被Tn特异性单克隆抗体识别。