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本文引用的文献

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Personal Neoantigen Cancer Vaccines: A Road Not Fully Paved.个体化新生抗原肿瘤疫苗:尚未完全铺就的道路。
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Synthesis of Carboxy-Dimethylmaleic Amide Linked Polymer Conjugate Based Ultra-pH-sensitive Nanoparticles for Enhanced Antitumor Immunotherapy.基于羧基-二甲基马来酰胺连接聚合物共轭物的超pH敏感纳米颗粒的合成用于增强抗肿瘤免疫治疗
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Adaptable antigen matrix platforms for peptide vaccination strategies and T cell-mediated anti-tumor immunity.用于肽疫苗接种策略和T细胞介导的抗肿瘤免疫的适应性抗原基质平台。
Biomaterials. 2020 Dec;262:120342. doi: 10.1016/j.biomaterials.2020.120342. Epub 2020 Aug 28.
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Human CLEC9A antibodies deliver NY-ESO-1 antigen to CD141 dendritic cells to activate naïve and memory NY-ESO-1-specific CD8 T cells.人 CLEC9A 抗体将 NY-ESO-1 抗原递呈给 CD141 树突状细胞,从而激活幼稚和记忆 NY-ESO-1 特异性 CD8 T 细胞。
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INeo-Epp: A Novel T-Cell HLA Class-I Immunogenicity or Neoantigenic Epitope Prediction Method Based on Sequence-Related Amino Acid Features.INeo-Epp:一种基于序列相关氨基酸特征的新型 T 细胞 HLA Ⅰ类免疫原性或新抗原表位预测方法。
Biomed Res Int. 2020 Jun 15;2020:5798356. doi: 10.1155/2020/5798356. eCollection 2020.
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Uncovering the Tumor Antigen Landscape: What to Know about the Discovery Process.揭示肿瘤抗原全景:关于发现过程需了解的内容。
Cancers (Basel). 2020 Jun 23;12(6):1660. doi: 10.3390/cancers12061660.
7
Impact of Cysteine Residues on MHC Binding Predictions and Recognition by Tumor-Reactive T Cells.半胱氨酸残基对 MHC 结合预测和肿瘤反应性 T 细胞识别的影响。
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Tuning antiviral CD8 T-cell response via proline-altered peptide ligand vaccination.通过脯氨酸修饰肽配体疫苗接种来调节抗病毒 CD8 T 细胞反应。
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An altered HLA-A0201-restricted MUC1 epitope that could induce more efficient anti-tumor effects against gastric cancer.一种改变的 HLA-A0201 限制性 MUC1 表位,可诱导针对胃癌的更有效的抗肿瘤作用。
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肿瘤免疫治疗中MHC-I表位预测的最新进展。

Recent progress on MHC-I epitope prediction in tumor immunotherapy.

作者信息

Wang Xiangyi, Yu Zhaojin, Liu Wensi, Tang Haichao, Yi Dongxu, Wei Minjie

机构信息

Department of Pharmacology, School of Pharmacy, China Medical University No. 77 Puhe Road, Shenyang North New District, Shenyang, Liaoning, P. R. China.

Liaoning Key Laboratory of Molecular Targeted Anti-Tumor Drug Development and Evaluation, China Medical University No. 77 Puhe Road, Shenyang North New District, Shenyang, Liaoning, P. R. China.

出版信息

Am J Cancer Res. 2021 Jun 15;11(6):2401-2416. eCollection 2021.

PMID:34249407
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8263640/
Abstract

Tumor immunotherapy has now become one of the most potential therapy for those intractable cancer diseases. The antigens on the cancer cell surfaces are the keys for the immune system to recognize and eliminate them. As reported, the immunogenicity of the tumor antigens could be determined by the binding between the key epitope peptides and MHC molecules. In recent years, the approaches to anticipate the peptides from the candidate epitopes have gradually changed into more efficient methods. Including the improved conventional methods, more diverse methods were coming into view. Here we review the anticipated methods of the tumor associated epitopes that specifically bind with major histocompatibility complex (MHC) class I molecules, and the recent advances and applications of those epitope prediction methods.

摘要

肿瘤免疫疗法现已成为治疗那些难治性癌症疾病最具潜力的疗法之一。癌细胞表面的抗原是免疫系统识别和清除它们的关键。据报道,肿瘤抗原的免疫原性可由关键表位肽与MHC分子之间的结合来决定。近年来,从候选表位预测肽的方法已逐渐转变为更有效的方法。包括改进的传统方法在内,更多样化的方法不断涌现。在此,我们综述了与主要组织相容性复合体(MHC)I类分子特异性结合的肿瘤相关表位的预测方法,以及这些表位预测方法的最新进展和应用。