Synthetic vaccines targeting Mincle through conjugation of trehalose dibehenate

Synthetic vaccines targeting Mincle through conjugation of trehalose dibehenate
复制标题

通过海藻糖二山嵛酸酯结合物靶向 Mincle 的合成疫苗

DOI:
10.1039/d2cc02100e
复制
发表时间:
2022
影响因子:
4.9
通讯作者:
Payne Richard J.
Payne Richard J.
中科院分区:
化学2区
文献类型:
--
作者:
Hanna Cameron C.;Maxwell Joshua W. C.;Ismanto Hendra S.;Ashhurst Anneliese S.;Artner Lukas M.;Rudrawar Santosh;Britton Warwick J.;Yamasaki Sho;Payne Richard J.

文献摘要

相似文献

免疫刺激佐剂与免疫原性抗原的共价融合是发展有效的传染病合成疫苗的一种有前途的策略。在这里,我们描述了来自6 kDa早期分泌抗原靶点(ESAT6)的分枝杆菌多肽抗原与适当功能化的海藻糖二乙酸酯(TDB)的偶联,TDB是一种有效的糖脂佐剂,靶向巨噬细胞诱导的C型凝集素(Mincle)。
The covalent fusion of immunostimulatory adjuvants to immunogenic antigens is a promising strategy for the development of effective synthetic vaccines for infectious diseases. Herein, we describe the conjugation of a mycobacterial peptide antigen from the 6 kDa early secretory antigenic target (ESAT6) to a suitably functionalised trehalose dibehenate (TDB), a potent glycolipid adjuvant targeting macrophage inducible C-type lectin (Mincle).