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Self-adjuvanting multicomponent cancer vaccine candidates combining per-glycosylated MUC1 glycopeptides and the Toll-like receptor 2 agonist Pam3CysSer.将全糖基化MUC1糖肽与Toll样受体2激动剂Pam3CysSer相结合的自佐剂多组分癌症疫苗候选物。
Angew Chem Int Ed Engl. 2011 Feb 11;50(7):1635-9. doi: 10.1002/anie.201006115. Epub 2011 Jan 7.
2
Synthesis of a monophosphoryl derivative of Escherichia coli lipid A and its efficient coupling to a tumor-associated carbohydrate antigen.大肠杆菌脂 A 的单磷酸酯衍生物的合成及其与肿瘤相关碳水化合物抗原的有效偶联。
Chemistry. 2010 Jan 25;16(4):1319-25. doi: 10.1002/chem.200902153.
3
Synthesis of a monophosphoryl lipid A derivative and its conjugation to a modified form of a tumor-associated carbohydrate antigen GM3.一种单磷酰脂质A衍生物的合成及其与肿瘤相关碳水化合物抗原GM3修饰形式的偶联。
Chem Commun (Camb). 2009 Oct 7(37):5536-7. doi: 10.1039/b907351e. Epub 2009 Aug 27.
4
Increasing the antigenicity of synthetic tumor-associated carbohydrate antigens by targeting Toll-like receptors.通过靶向Toll样受体提高合成肿瘤相关碳水化合物抗原的抗原性
Chembiochem. 2009 Feb 13;10(3):455-63. doi: 10.1002/cbic.200800596.
5
Synthetic and immunological studies of 5'-N-phenylacetyl sTn to develop carbohydrate-based cancer vaccines and to explore the impacts of linkage between carbohydrate antigens and carrier proteins.5'-N-苯乙酰化唾液酸化Tn的合成与免疫学研究,以开发基于碳水化合物的癌症疫苗并探索碳水化合物抗原与载体蛋白之间连接的影响。
Bioconjug Chem. 2008 Oct;19(10):2060-7. doi: 10.1021/bc800243f. Epub 2008 Sep 25.
6
Putting endotoxin to work for us: monophosphoryl lipid A as a safe and effective vaccine adjuvant.让内毒素为我们所用:单磷酰脂质A作为一种安全有效的疫苗佐剂。
Cell Mol Life Sci. 2008 Oct;65(20):3231-40. doi: 10.1007/s00018-008-8228-6.
7
Towards a self-adjuvanting multivalent B and T cell epitope containing synthetic glycolipopeptide cancer vaccine.迈向一种含合成糖脂肽癌症疫苗的自佐剂多价B细胞和T细胞表位。
ChemMedChem. 2008 May;3(5):737-41. doi: 10.1002/cmdc.200700315.
8
Efficient glycoengineering of GM3 on melanoma cell and monoclonal antibody-mediated selective killing of the glycoengineered cancer cell.黑色素瘤细胞上GM3的高效糖基工程改造以及单克隆抗体介导的对糖基工程改造癌细胞的选择性杀伤。
Bioorg Med Chem. 2007 Dec 15;15(24):7561-7. doi: 10.1016/j.bmc.2007.09.005. Epub 2007 Sep 12.
9
Modulation of innate immune responses with synthetic lipid A derivatives.用合成脂多糖A衍生物调节天然免疫反应。
J Am Chem Soc. 2007 Apr 25;129(16):5200-16. doi: 10.1021/ja068922a. Epub 2007 Mar 29.
10
Improving the antigenicity of sTn antigen by modification of its sialic acid residue for development of glycoconjugate cancer vaccines.通过修饰其唾液酸残基提高sTn抗原的抗原性以开发糖缀合物癌症疫苗。
Bioconjug Chem. 2006 Nov-Dec;17(6):1537-44. doi: 10.1021/bc060103s.

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.

DOI:10.1021/cb200358r
PMID:22013921
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3262944/
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。