• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

为设计抗癌疫苗而了解抗原交叉呈递的生物学机制。

Understanding the biology of antigen cross-presentation for the design of vaccines against cancer.

作者信息

Fehres Cynthia M, Unger Wendy W J, Garcia-Vallejo Juan J, van Kooyk Yvette

机构信息

Department of Molecular Cell Biology and Immunology, VU University Medical Center , Amsterdam , Netherlands.

出版信息

Front Immunol. 2014 Apr 8;5:149. doi: 10.3389/fimmu.2014.00149. eCollection 2014.

DOI:10.3389/fimmu.2014.00149
PMID:24782858
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3986565/
Abstract

Antigen cross-presentation, the process in which exogenous antigens are presented on MHC class I molecules, is crucial for the generation of effector CD8(+) T cell responses. Although multiple cell types are being described to be able to cross-present antigens, in vivo this task is mainly carried out by certain subsets of dendritic cells (DCs). Aspects such as the internalization route, the pathway of endocytic trafficking, and the simultaneous activation through pattern-recognition receptors have a determining influence in how antigens are handled for cross-presentation by DCs. In this review, we will summarize new insights in factors that affect antigen cross-presentation of human DC subsets, and we will discuss the possibilities to exploit antigen cross-presentation for immunotherapy against cancer.

摘要

抗原交叉呈递是指外源性抗原在MHC I类分子上呈递的过程,对于效应性CD8(+) T细胞反应的产生至关重要。尽管多种细胞类型被描述为能够交叉呈递抗原,但在体内这项任务主要由特定亚群的树突状细胞(DC)执行。内化途径、内吞运输途径以及通过模式识别受体的同时激活等方面,对DC如何处理抗原以进行交叉呈递具有决定性影响。在本综述中,我们将总结影响人类DC亚群抗原交叉呈递的因素的新见解,并讨论利用抗原交叉呈递进行癌症免疫治疗的可能性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6e70/3986565/04a0d516e9e3/fimmu-05-00149-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6e70/3986565/f8dfb1063c3d/fimmu-05-00149-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6e70/3986565/04a0d516e9e3/fimmu-05-00149-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6e70/3986565/f8dfb1063c3d/fimmu-05-00149-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6e70/3986565/04a0d516e9e3/fimmu-05-00149-g002.jpg

相似文献

1
Understanding the biology of antigen cross-presentation for the design of vaccines against cancer.为设计抗癌疫苗而了解抗原交叉呈递的生物学机制。
Front Immunol. 2014 Apr 8;5:149. doi: 10.3389/fimmu.2014.00149. eCollection 2014.
2
Toll-Like Receptor 4 Triggering Promotes Cytosolic Routing of DC-SIGN-Targeted Antigens for Presentation on MHC Class I.Toll 样受体 4 触发促进了 DC-SIGN 靶向抗原的细胞溶质途径,用于 MHC Ⅰ类分子的呈递。
Front Immunol. 2018 Jun 14;9:1231. doi: 10.3389/fimmu.2018.01231. eCollection 2018.
3
Dendritic cell-targeted vaccines.树突状细胞靶向疫苗。
Front Immunol. 2014 May 30;5:255. doi: 10.3389/fimmu.2014.00255. eCollection 2014.
4
Dendritic cell biology and its role in tumor immunotherapy.树突状细胞生物学及其在肿瘤免疫治疗中的作用。
J Hematol Oncol. 2020 Aug 3;13(1):107. doi: 10.1186/s13045-020-00939-6.
5
Sustained cross-presentation capacity of murine splenic dendritic cell subsets in vivo.体内鼠脾脏树突状细胞亚群持续的交叉呈递能力。
Eur J Immunol. 2018 Jul;48(7):1164-1173. doi: 10.1002/eji.201747372. Epub 2018 May 17.
6
Endocytic Recycling of MHC Class I Molecules in Non-professional Antigen Presenting and Dendritic Cells.MHC I 类分子在内吞体中的再循环:非专业抗原提呈细胞和树突状细胞。
Front Immunol. 2019 Jan 7;9:3098. doi: 10.3389/fimmu.2018.03098. eCollection 2018.
7
Glycan-based DC-SIGN targeting vaccines to enhance antigen cross-presentation.基于聚糖的树突状细胞特异性细胞间黏附分子-3 结合非黏附分子靶向疫苗增强抗原交叉呈递。
Mol Immunol. 2013 Sep;55(2):143-5. doi: 10.1016/j.molimm.2012.10.031. Epub 2012 Nov 14.
8
Intracellular Transport Routes for MHC I and Their Relevance for Antigen Cross-Presentation.MHC I的细胞内运输途径及其与抗原交叉呈递的相关性。
Front Immunol. 2015 Jul 2;6:335. doi: 10.3389/fimmu.2015.00335. eCollection 2015.
9
Engineering anti-cancer nanovaccine based on antigen cross-presentation.基于抗原交叉呈递的工程抗癌纳米疫苗。
Biosci Rep. 2019 Oct 30;39(10). doi: 10.1042/BSR20193220.
10
MHC class I endosomal and lysosomal trafficking coincides with exogenous antigen loading in dendritic cells.MHC I类分子在内体和溶酶体中的运输与树突状细胞中外源抗原的加载过程相吻合。
PLoS One. 2008 Sep 19;3(9):e3247. doi: 10.1371/journal.pone.0003247.

引用本文的文献

1
A scaffold vaccine to promote tumor antigen cross-presentation sustained toll-like receptor-2 (TLR2) activation.一种促进肿瘤抗原交叉呈递并持续激活Toll样受体2(TLR2)的支架疫苗。
Bioact Mater. 2024 Apr 23;37:315-330. doi: 10.1016/j.bioactmat.2024.03.035. eCollection 2024 Jul.
2
Sec22b and Stx4 Depletion Has No Major Effect on Cross-Presentation of PLGA Microsphere-Encapsulated Antigen and a Synthetic Long Peptide In Vitro.Sec22b 和 Stx4 耗竭对 PLGA 微球包封抗原和合成长肽的体外交叉呈递无主要影响。
J Immunol. 2023 Oct 15;211(8):1203-1215. doi: 10.4049/jimmunol.2200473.
3
Reinforcement of cell-mediated immunity driven by tumor-associated Epstein-Barr virus (EBV)-specific T cells during targeted B-cell therapy with rituximab.

本文引用的文献

1
Substrate-induced protein stabilization reveals a predominant contribution from mature proteins to peptides presented on MHC class I.底物诱导的蛋白质稳定揭示了成熟蛋白质对 MHC I 类呈递的肽的主要贡献。
J Immunol. 2013 Dec 1;191(11):5410-9. doi: 10.4049/jimmunol.1300078. Epub 2013 Oct 30.
2
Targeting uptake receptors on human plasmacytoid dendritic cells triggers antigen cross-presentation and robust type I IFN secretion.靶向人浆细胞样树突状细胞上的摄取受体可触发抗原交叉呈递和强烈的 I 型 IFN 分泌。
J Immunol. 2013 Nov 15;191(10):5005-12. doi: 10.4049/jimmunol.1300787. Epub 2013 Oct 14.
3
Up-regulation of PD-L1, IDO, and T(regs) in the melanoma tumor microenvironment is driven by CD8(+) T cells.
在利妥昔单抗靶向 B 细胞治疗过程中,肿瘤相关 EBV 特异性 T 细胞驱动的细胞介导免疫增强。
Front Immunol. 2023 Mar 24;14:878953. doi: 10.3389/fimmu.2023.878953. eCollection 2023.
4
Canvassing Prospects of Glyco-Nanovaccines for Developing Cross-Presentation Mediated Anti-Tumor Immunotherapy.探索糖基纳米疫苗在开发交叉呈递介导的抗肿瘤免疫疗法方面的前景。
Vaccines (Basel). 2022 Nov 30;10(12):2049. doi: 10.3390/vaccines10122049.
5
Structural and biochemical characteristics of mRNA nanoparticles determine anti-SARS-CoV-2 humoral and cellular immune responses.mRNA 纳米颗粒的结构和生化特性决定了抗 SARS-CoV-2 的体液和细胞免疫反应。
Sci Adv. 2022 Nov 25;8(47):eabo1827. doi: 10.1126/sciadv.abo1827. Epub 2022 Nov 23.
6
Nanotechnology-facilitated vaccine development during the coronavirus disease 2019 (COVID-19) pandemic.2019冠状病毒病(COVID-19)大流行期间纳米技术助力疫苗研发
Exploration (Beijing). 2022 Jul 21;2(5):20210082. doi: 10.1002/EXP.20210082.
7
Optimized mobilization of MHC class I- and II- restricted immunity by dendritic cell vaccine potentiates cancer therapy.树突状细胞疫苗增强 MHC Ⅰ类和Ⅱ类限制性免疫的优化动员可增强癌症治疗效果。
Theranostics. 2022 Apr 24;12(7):3488-3502. doi: 10.7150/thno.71760. eCollection 2022.
8
CD206+ tumor-associated macrophages cross-present tumor antigen and drive antitumor immunity.CD206+ 肿瘤相关巨噬细胞交叉呈递肿瘤抗原并驱动抗肿瘤免疫。
JCI Insight. 2022 Jun 8;7(11):e155022. doi: 10.1172/jci.insight.155022.
9
Breast Cancer Tumor Microenvironment and Molecular Aberrations Hijack Tumoricidal Immunity.乳腺癌肿瘤微环境与分子畸变劫持肿瘤杀伤性免疫。
Cancers (Basel). 2022 Jan 7;14(2):285. doi: 10.3390/cancers14020285.
10
Antigen-Capturing Mesoporous Silica Nanoparticles Enhance the Radiation-Induced Abscopal Effect in Murine Hepatocellular Carcinoma Hepa1-6 Models.抗原捕获介孔二氧化硅纳米颗粒增强小鼠肝细胞癌Hepa1-6模型中的辐射诱导远隔效应。
Pharmaceutics. 2021 Oct 29;13(11):1811. doi: 10.3390/pharmaceutics13111811.
在黑色素瘤肿瘤微环境中,PD-L1、IDO 和 T(regs)的上调是由 CD8(+) T 细胞驱动的。
Sci Transl Med. 2013 Aug 28;5(200):200ra116. doi: 10.1126/scitranslmed.3006504.
4
Human CD1c+ dendritic cells secrete high levels of IL-12 and potently prime cytotoxic T-cell responses.人 CD1c+树突状细胞分泌高水平的 IL-12,并有力地启动细胞毒性 T 细胞反应。
Blood. 2013 Aug 8;122(6):932-42. doi: 10.1182/blood-2013-04-495424. Epub 2013 Jun 21.
5
Indoleamine 2,3-dioxygenase is a critical resistance mechanism in antitumor T cell immunotherapy targeting CTLA-4.吲哚胺 2,3-双加氧酶是针对 CTLA-4 的抗肿瘤 T 细胞免疫治疗中的关键耐药机制。
J Exp Med. 2013 Jul 1;210(7):1389-402. doi: 10.1084/jem.20130066. Epub 2013 Jun 10.
6
Dynamic imaging reveals promiscuous crosspresentation of blood-borne antigens to naive CD8+ T cells in the bone marrow.动态成像揭示了血液源性抗原在骨髓中向幼稚 CD8+T 细胞的混杂交叉呈递。
Blood. 2013 Jul 11;122(2):193-208. doi: 10.1182/blood-2012-01-401265. Epub 2013 May 1.
7
Strength of PD-1 signaling differentially affects T-cell effector functions.PD-1 信号的强度会对 T 细胞效应功能产生不同影响。
Proc Natl Acad Sci U S A. 2013 Jul 2;110(27):E2480-9. doi: 10.1073/pnas.1305394110. Epub 2013 Apr 22.
8
Antigen delivery to early endosomes eliminates the superiority of human blood BDCA3+ dendritic cells at cross presentation.抗原递送至早期内体消除了人血 BDCA3+树突状细胞在交叉呈递中的优势。
J Exp Med. 2013 May 6;210(5):1049-63. doi: 10.1084/jem.20121251. Epub 2013 Apr 8.
9
Antigen cross-presentation by dendritic cell subsets: one general or all sergeants?树突状细胞亚群的抗原交叉呈递:一视同仁还是各有所长?
Trends Immunol. 2013 Aug;34(8):361-70. doi: 10.1016/j.it.2013.02.007. Epub 2013 Mar 27.
10
Intradermal delivery of TLR agonists in a human explant skin model: preferential activation of migratory dendritic cells by polyribosinic-polyribocytidylic acid and peptidoglycans.TLR 激动剂在人体皮肤外植体模型中的皮内递送:多聚核糖核苷酸多聚胞嘧啶核苷酸和肽聚糖优先激活迁移树突状细胞。
J Immunol. 2013 Apr 1;190(7):3338-45. doi: 10.4049/jimmunol.1200598. Epub 2013 Mar 6.