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本文引用的文献

1
Transient antibody-antigen interactions mediate the strain-specific recognition of a conserved malaria epitope.瞬时抗体-抗原相互作用介导了对保守疟疾表位的菌株特异性识别。
Commun Biol. 2018 May 31;1:58. doi: 10.1038/s42003-018-0063-1. eCollection 2018.
2
Natural Parasite Exposure Induces Protective Human Anti-Malarial Antibodies.自然接触寄生虫可诱导人体产生保护性抗疟抗体。
Immunity. 2017 Dec 19;47(6):1197-1209.e10. doi: 10.1016/j.immuni.2017.11.007. Epub 2017 Nov 29.
3
A virus-like particle of the hepatitis B virus preS antigen elicits robust neutralizing antibodies and T cell responses in mice.乙型肝炎病毒前 S 抗原病毒样颗粒在小鼠中引发强烈的中和抗体和 T 细胞反应。
Antiviral Res. 2018 Jan;149:48-57. doi: 10.1016/j.antiviral.2017.11.007. Epub 2017 Nov 10.
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Peptide-based synthetic vaccines.基于肽的合成疫苗。
Chem Sci. 2016 Feb 1;7(2):842-854. doi: 10.1039/c5sc03892h. Epub 2015 Dec 17.
5
T-dependent B cell responses to Plasmodium induce antibodies that form a high-avidity multivalent complex with the circumsporozoite protein.对疟原虫的T细胞依赖性B细胞反应诱导产生抗体,这些抗体与环子孢子蛋白形成高亲和力的多价复合物。
PLoS Pathog. 2017 Jul 31;13(7):e1006469. doi: 10.1371/journal.ppat.1006469. eCollection 2017 Jul.
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Cancer immunotherapy: moving forward with peptide T cell vaccines.癌症免疫疗法:用肽 T 细胞疫苗推进。
Curr Opin Immunol. 2017 Aug;47:57-63. doi: 10.1016/j.coi.2017.07.003. Epub 2017 Jul 19.
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Lipid interactions modulate the structural and antigenic properties of the C-terminal domain of the malaria antigen merozoite surface protein 2.脂质相互作用调节疟疾抗原裂殖子表面蛋白2 C末端结构域的结构和抗原特性。
FEBS J. 2017 Aug;284(16):2649-2662. doi: 10.1111/febs.14135. Epub 2017 Jul 5.
8
A third generation vaccine for human visceral leishmaniasis and post kala azar dermal leishmaniasis: First-in-human trial of ChAd63-KH.用于人类内脏利什曼病和黑热病后皮肤利什曼病的第三代疫苗:ChAd63-KH的首次人体试验。
PLoS Negl Trop Dis. 2017 May 12;11(5):e0005527. doi: 10.1371/journal.pntd.0005527. eCollection 2017 May.
9
Structure and Characterisation of a Key Epitope in the Conserved C-Terminal Domain of the Malaria Vaccine Candidate MSP2.疟疾疫苗候选抗原MSP2保守C端结构域中关键表位的结构与鉴定
J Mol Biol. 2017 Mar 24;429(6):836-846. doi: 10.1016/j.jmb.2017.02.003. Epub 2017 Feb 8.
10
Ligand-induced Epitope Masking: DISSOCIATION OF INTEGRIN α5β1-FIBRONECTIN COMPLEXES ONLY BY MONOCLONAL ANTIBODIES WITH AN ALLOSTERIC MODE OF ACTION.配体诱导的表位掩盖:仅通过具有变构作用模式的单克隆抗体解离整合素α5β1-纤连蛋白复合物
J Biol Chem. 2016 Sep 30;291(40):20993-21007. doi: 10.1074/jbc.M116.736942. Epub 2016 Aug 2.

作为肽疫苗的无序表位

Disordered epitopes as peptide vaccines.

作者信息

MacRaild Christopher A, Seow Jeffrey, Das Sreedam C, Norton Raymond S

机构信息

Medicinal Chemistry, Monash Institute of Pharmaceutical Sciences, Monash University, 381 Royal Parade Parkville 3052 Australia.

出版信息

Pept Sci (Hoboken). 2018 May;110(3):e24067. doi: 10.1002/pep2.24067. Epub 2018 Apr 14.

DOI:10.1002/pep2.24067
PMID:32328540
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7167742/
Abstract

The development of clinically useful peptide-based vaccines remains a long-standing goal. This review highlights that intrinsically disordered protein antigens, which lack an ordered three-dimensional structure, represent excellent starting points for the development of such vaccines. Disordered proteins represent an important class of antigen in a wide range of human pathogens, and, contrary to widespread belief, they are frequently targets of protective antibody responses. Importantly, disordered epitopes appear invariably to be linear epitopes, rendering them ideally suited to incorporation into a peptide vaccine. Nonetheless, the conformational properties of disordered antigens, and hence their recognition by antibodies, frequently depend on the interactions they make and the context in which they are presented to the immune system. These effects must be considered in the design of an effective vaccine. Here we discuss these issues and propose design principles that may facilitate the development of peptide vaccines targeting disordered antigens.

摘要

开发临床上有用的基于肽的疫苗仍然是一个长期目标。本综述强调,缺乏有序三维结构的内在无序蛋白抗原是开发此类疫苗的理想起点。无序蛋白是多种人类病原体中的一类重要抗原,与普遍看法相反,它们经常是保护性抗体反应的靶点。重要的是,无序表位似乎总是线性表位,这使其非常适合纳入肽疫苗。尽管如此,无序抗原的构象特性,以及因此它们被抗体识别的情况,通常取决于它们所形成的相互作用以及它们呈递给免疫系统的背景。在设计有效的疫苗时必须考虑这些影响。在这里,我们讨论这些问题并提出可能有助于开发针对无序抗原的肽疫苗的设计原则。