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碳水化合物-单磷酸脂质 A 缀合物是完全合成的自佐剂癌症疫苗,在小鼠中引发强烈的免疫反应。

Carbohydrate-monophosphoryl lipid a conjugates are fully synthetic self-adjuvanting cancer vaccines eliciting robust immune responses in the mouse.

机构信息

Department of Chemistry, Wayne State University, Detroit, Michigan 48202, United States.

出版信息

ACS Chem Biol. 2012 Jan 20;7(1):235-40. doi: 10.1021/cb200358r. Epub 2011 Nov 1.

Abstract

Tumor-associated carbohydrate antigens (TACAs) are useful targets in the development of therapeutic cancer vaccines. However, a serious problem with them is the poor immunogenicity. To overcome the problem, a monophosphorylated derivative of Neisseria meningitidis lipid A was explored as a potential carrier molecule and built-in adjuvant for the construction of structurally defined fully synthetic glycoconjugate vaccines. Some paradigm-shifting discoveries about the monophosphoryl lipid A (MPLA)-TACA conjugates were that they elicited robust IgG antibody responses, indicating T cell-mediated immunity, without an external adjuvant and that an external adjuvant, e.g., Titermax Gold, actually reduced rather than promoted the immunological activity of the conjugates. The induced antibodies were proved to bind selectively to target tumor cells. MPLA was therefore demonstrated to be a powerful built-in immunostimulant and adjuvant for an all new design of fully synthetic glycoconjugate cancer vaccines.

摘要

肿瘤相关碳水化合物抗原(TACAs)是开发治疗性癌症疫苗的有用靶点。然而,它们存在一个严重的问题,即免疫原性差。为了解决这个问题,研究了脑膜炎奈瑟菌脂 A 的单磷酸化衍生物作为一种潜在的载体分子和内置佐剂,用于构建结构明确的全合成糖缀合物疫苗。关于单磷酸化脂质 A(MPLA)-TACA 缀合物的一些突破性发现是,它们在没有外源性佐剂的情况下引发了强烈的 IgG 抗体反应,表明 T 细胞介导的免疫,而外源性佐剂,如 Titermax Gold,则实际上降低了缀合物的免疫活性,而不是促进了其免疫活性。诱导的抗体被证明能选择性地与靶肿瘤细胞结合。因此,MPLA 被证明是一种强大的内置免疫刺激剂和佐剂,用于全新设计的全合成糖缀合物癌症疫苗。

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