Vichier-Guerre Sophie, Lo-Man Richard, Huteau Valérie, Dériaud Edith, Leclerc Claude, Bay Sylvie
Unité de Chimie Organique URA CNRS 2128, Institut Pasteur, 28, rue du Dr Roux, 75724 Paris 15, France.
Bioorg Med Chem Lett. 2004 Jul 5;14(13):3567-70. doi: 10.1016/j.bmcl.2004.04.047.
As part of our program on Tn-specific anti-tumor immunotherapy, our aim was to vary the nature of the aglyconic part of the tumor-associated Tn antigen (alpha-d-GalNAc-Ser/Thr). This report describes the synthesis of Fmoc-hSer-(alpha-d-GalNAc)-OH (4) in 19% overall yield from protected aspartic acid. The building block 4 was incorporated as trimeric clusters into a glycopeptide vaccine [MAG:Tn(hSer)3-PV], using solid-phase peptide synthesis. When injected in mice, the resulting MAG induces a strong antibody response, which recognizes native tumor-associated antigens (TAA) at the surface of human tumor cells. This approach may be extended to the use of other nonnatural TAA in order to improve half-life of synthetic anti-cancer vaccines.
作为我们Tn特异性抗肿瘤免疫治疗项目的一部分,我们的目标是改变肿瘤相关Tn抗原(α-d-氨基半乳糖-Ser/Thr)苷元部分的性质。本报告描述了从保护的天冬氨酸出发,以19%的总收率合成Fmoc-hSer-(α-d-氨基半乳糖)-OH(4)。使用固相肽合成法,将构建块4作为三聚体簇掺入糖肽疫苗[MAG:Tn(hSer)3-PV]中。当注射到小鼠体内时,所得的MAG诱导强烈的抗体反应,该反应可识别人类肿瘤细胞表面的天然肿瘤相关抗原(TAA)。这种方法可能会扩展到使用其他非天然TAA,以提高合成抗癌疫苗的半衰期。