• 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

糖的多种口味:通过C型凝集素受体进行糖基化在靶向和调节人类免疫方面的潜力

Various Tastes of Sugar: The Potential of Glycosylation in Targeting and Modulating Human Immunity via C-Type Lectin Receptors.

作者信息

Busold Stefanie, Nagy Noémi A, Tas Sander W, van Ree Ronald, de Jong Esther C, Geijtenbeek Teunis B H

机构信息

Department of Experimental Immunology, Amsterdam University Medical Centers, Amsterdam Institute for Infection and Immunity, University of Amsterdam, Amsterdam, Netherlands.

Department of Rheumatology and Clinical Immunology, Amsterdam University Medical Centers, Amsterdam Rheumatology and Immunology Center, University of Amsterdam, Amsterdam, Netherlands.

出版信息

Front Immunol. 2020 Feb 7;11:134. doi: 10.3389/fimmu.2020.00134. eCollection 2020.

DOI:10.3389/fimmu.2020.00134
PMID:32117281
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7019010/
Abstract

C-type lectin receptors (CLRs) are important in several immune regulatory processes. These receptors recognize glycans expressed by host cells or by pathogens. Whereas pathogens are recognized through their glycans, which leads to protective immunity, aberrant cellular glycans are now increasingly recognized as disease-driving factors in cancer, auto-immunity, and allergy. The vast variety of glycan structures translates into a wide spectrum of effects on the immune system ranging from immune suppression to hyper-inflammatory responses. CLRs have distinct expression patterns on antigen presenting cells (APCs) controlling their role in immunity. CLRs can also be exploited to selectively target specific APCs, modulate immune responses and enhance antigen presentation. Here we will discuss the role of glycans and their receptors in immunity as well as potential strategies for immune modulation. A special focus will be given to different dendritic cell subsets as these APCs are crucial orchestrators of immune responses in infections, cancer, auto-immunity and allergies. Furthermore, we will highlight the potential use of nanoscale lipid bi-layer structures (liposomes) in targeted immunotherapy.

摘要

C型凝集素受体(CLRs)在多个免疫调节过程中发挥重要作用。这些受体可识别宿主细胞或病原体表达的聚糖。病原体通过其聚糖被识别,从而引发保护性免疫,而异常的细胞聚糖如今越来越被视为癌症、自身免疫和过敏等疾病的驱动因素。多种多样的聚糖结构对免疫系统产生广泛影响,从免疫抑制到过度炎症反应不等。CLRs在抗原呈递细胞(APC)上具有独特的表达模式,从而控制其在免疫中的作用。CLRs还可用于选择性靶向特定的APC,调节免疫反应并增强抗原呈递。在此,我们将讨论聚糖及其受体在免疫中的作用以及免疫调节的潜在策略。我们将特别关注不同的树突状细胞亚群,因为这些APC是感染、癌症、自身免疫和过敏中免疫反应的关键协调者。此外,我们将强调纳米级脂质双分子层结构(脂质体)在靶向免疫治疗中的潜在用途。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1309/7019010/83064aeb3851/fimmu-11-00134-g0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1309/7019010/105ffd4c1621/fimmu-11-00134-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1309/7019010/836be1ae36e2/fimmu-11-00134-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1309/7019010/83064aeb3851/fimmu-11-00134-g0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1309/7019010/105ffd4c1621/fimmu-11-00134-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1309/7019010/836be1ae36e2/fimmu-11-00134-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1309/7019010/83064aeb3851/fimmu-11-00134-g0003.jpg

相似文献

1
Various Tastes of Sugar: The Potential of Glycosylation in Targeting and Modulating Human Immunity via C-Type Lectin Receptors.糖的多种口味:通过C型凝集素受体进行糖基化在靶向和调节人类免疫方面的潜力
Front Immunol. 2020 Feb 7;11:134. doi: 10.3389/fimmu.2020.00134. eCollection 2020.
2
Glycan-Based Cell Targeting To Modulate Immune Responses.基于聚糖的细胞靶向调节免疫反应。
Trends Biotechnol. 2017 Apr;35(4):334-346. doi: 10.1016/j.tibtech.2016.10.002. Epub 2016 Oct 27.
3
Using the glycan toolbox for pathogenic interventions and glycan immunotherapy.利用聚糖工具包进行致病干预和聚糖免疫治疗。
Curr Opin Biotechnol. 2018 Jun;51:24-31. doi: 10.1016/j.copbio.2017.11.003. Epub 2017 Nov 22.
4
Myeloid C-type lectin receptors in host-pathogen interactions and glycan-based targeting.宿主-病原体相互作用和基于聚糖的靶向中的髓样 C 型凝集素受体。
Curr Opin Chem Biol. 2024 Oct;82:102521. doi: 10.1016/j.cbpa.2024.102521. Epub 2024 Aug 29.
5
Dendritic cells and C-type lectin receptors: coupling innate to adaptive immune responses.树突状细胞与C型凝集素受体:连接固有免疫与适应性免疫反应
Immunol Cell Biol. 2008 Oct;86(7):580-7. doi: 10.1038/icb.2008.55. Epub 2008 Aug 5.
6
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.
7
Cross-presentation through langerin and DC-SIGN targeting requires different formulations of glycan-modified antigens.通过 langerin 和 DC-SIGN 靶向的交叉呈递需要不同形式的糖基化修饰抗原。
J Control Release. 2015 Apr 10;203:67-76. doi: 10.1016/j.jconrel.2015.01.040. Epub 2015 Feb 2.
8
Glycans from avian influenza virus are recognized by chicken dendritic cells and are targets for the humoral immune response in chicken.禽类流感病毒的聚糖可被鸡树突状细胞识别,是鸡体体液免疫应答的靶标。
Mol Immunol. 2013 Dec;56(4):452-62. doi: 10.1016/j.molimm.2013.06.007. Epub 2013 Aug 1.
9
C-Type Lectin Receptor Mediated Modulation of T2 Immune Responses to Allergens.C 型凝集素受体介导的变应原 T2 免疫应答调节。
Curr Allergy Asthma Rep. 2023 Mar;23(3):141-151. doi: 10.1007/s11882-023-01067-0. Epub 2023 Feb 1.
10
Plant lectins and their usage in preparing targeted nanovaccines for cancer immunotherapy.植物凝集素及其在制备用于癌症免疫治疗的靶向纳米疫苗中的应用。
Semin Cancer Biol. 2022 May;80:87-106. doi: 10.1016/j.semcancer.2020.02.005. Epub 2020 Feb 14.

引用本文的文献

1
Immunogenicity of mannan derived from as a promising adjuvant in vaccine BCG.源自卡介苗的甘露聚糖作为一种有前景的疫苗佐剂的免疫原性。
Iran J Microbiol. 2024 Jun;16(3):351-356. doi: 10.18502/ijm.v16i3.15767.
2
Advancing immunotherapy using biomaterials to control tissue, cellular, and molecular level immune signaling in skin.利用生物材料推进免疫疗法,以控制皮肤组织、细胞和分子水平的免疫信号。
Adv Drug Deliv Rev. 2024 Jun;209:115315. doi: 10.1016/j.addr.2024.115315. Epub 2024 Apr 25.
3
Straight to the point: targeted mRNA-delivery to immune cells for improved vaccine design.

本文引用的文献

1
Yeast-Derived β-Glucan in Cancer: Novel Uses of a Traditional Therapeutic.酵母衍生β-葡聚糖在癌症中的应用:传统治疗方法的新用途。
Int J Mol Sci. 2019 Jul 24;20(15):3618. doi: 10.3390/ijms20153618.
2
S-Layer Glycoprotein From Exerts Its Immunostimulatory Activity Through Glycan Recognition by Mincle.S-层糖蛋白 通过 Mincle 识别聚糖发挥其免疫刺激活性。
Front Immunol. 2019 Jun 26;10:1422. doi: 10.3389/fimmu.2019.01422. eCollection 2019.
3
Costimulatory Molecules and Immune Checkpoints Are Differentially Expressed on Different Subsets of Dendritic Cells.
直切要点:靶向免疫细胞的 mRNA 递送,用于改良疫苗设计。
Front Immunol. 2023 Nov 27;14:1294929. doi: 10.3389/fimmu.2023.1294929. eCollection 2023.
4
Ligand Recognition by the Macrophage Galactose-Type C-Type Lectin: Self or Non-Self?-A Way to Trick the Host's Immune System.巨噬细胞半乳糖型 C 型凝集素的配体识别:自身或非自身?——一种欺骗宿主免疫系统的方法。
Int J Mol Sci. 2023 Dec 3;24(23):17078. doi: 10.3390/ijms242317078.
5
A tumor-associated heparan sulfate-related glycosaminoglycan promotes the generation of functional regulatory T cells.一种与肿瘤相关的肝素硫酸相关糖胺聚糖促进功能性调节性 T 细胞的生成。
Cell Mol Immunol. 2023 Dec;20(12):1499-1512. doi: 10.1038/s41423-023-01096-9. Epub 2023 Nov 22.
6
The melanoma tumor glyco-code impacts human dendritic cells' functionality and dictates clinical outcomes.黑色素瘤肿瘤糖码影响人类树突状细胞的功能,并决定临床结果。
Front Immunol. 2023 Feb 20;14:1120434. doi: 10.3389/fimmu.2023.1120434. eCollection 2023.
7
Unique CLR expression patterns on circulating and tumor-infiltrating DC subsets correlated with clinical outcome in melanoma patients.循环和肿瘤浸润 DC 亚群上独特的 CLR 表达模式与黑色素瘤患者的临床结局相关。
Front Immunol. 2022 Oct 24;13:1040600. doi: 10.3389/fimmu.2022.1040600. eCollection 2022.
8
Seminal Plasma Glycoproteins as Potential Ligands of Lectins Engaged in Immunity Regulation.精浆糖蛋白作为参与免疫调节的凝集素的潜在配体。
Int J Environ Res Public Health. 2022 Aug 23;19(17):10489. doi: 10.3390/ijerph191710489.
9
Nanoparticles for Inducing Antigen-Specific T Cell Tolerance in Autoimmune Diseases.用于诱导自身免疫性疾病中抗原特异性 T 细胞耐受的纳米颗粒。
Front Immunol. 2022 Mar 22;13:864403. doi: 10.3389/fimmu.2022.864403. eCollection 2022.
10
Direct and indirect engagement of dendritic cell function by antibodies developed for cancer therapy.用于癌症治疗的抗体对树突状细胞功能的直接和间接作用。
Clin Exp Immunol. 2022 Jul 22;209(1):64-71. doi: 10.1093/cei/uxac026.
共刺激分子和免疫检查点在不同亚群的树突状细胞上呈差异性表达。
Front Immunol. 2019 Jun 11;10:1325. doi: 10.3389/fimmu.2019.01325. eCollection 2019.
4
A Specific, Glycomimetic Langerin Ligand for Human Langerhans Cell Targeting.一种用于靶向人朗格汉斯细胞的特异性糖模拟物朗格素配体。
ACS Cent Sci. 2019 May 22;5(5):808-820. doi: 10.1021/acscentsci.9b00093. Epub 2019 May 10.
5
N-Linked Glycans in the Variable Domain of IgG Anti-Citrullinated Protein Antibodies Predict the Development of Rheumatoid Arthritis.IgG 抗瓜氨酸化蛋白抗体可变区中的 N-连接聚糖可预测类风湿关节炎的发生。
Arthritis Rheumatol. 2019 Oct;71(10):1626-1633. doi: 10.1002/art.40920. Epub 2019 Sep 2.
6
In vitro activation and maturation of human mononuclear phagocytes by stimulation with liposomes coated with a neoglycolipid containing α1-3, α1-6-mannotriose.用含有α1-3、α1-6-甘露三糖的新糖脂修饰的脂质体刺激人单核吞噬细胞,体外激活和成熟。
Glycoconj J. 2019 Jun;36(3):185-197. doi: 10.1007/s10719-019-09870-6. Epub 2019 Apr 23.
7
Tolerogenic Dendritic Cells and T-Regulatory Cells at the Clinical Trials Crossroad for the Treatment of Autoimmune Disease; Emphasis on Type 1 Diabetes Therapy.免疫耐受树突状细胞和调节性 T 细胞在治疗自身免疫性疾病的临床试验十字路口;重点是 1 型糖尿病治疗。
Front Immunol. 2019 Feb 6;10:148. doi: 10.3389/fimmu.2019.00148. eCollection 2019.
8
Antigens reversibly conjugated to a polymeric glyco-adjuvant induce protective humoral and cellular immunity.抗原可逆地与聚合糖佐剂结合,诱导保护性体液和细胞免疫。
Nat Mater. 2019 Feb;18(2):175-185. doi: 10.1038/s41563-018-0256-5. Epub 2019 Jan 14.
9
Novel vaccines targeting dendritic cells by coupling allergoids to mannan.通过将变应原类提取物与甘露聚糖偶联来靶向树突状细胞的新型疫苗。
Allergo J Int. 2018;27(8):256-262. doi: 10.1007/s40629-018-0069-8. Epub 2018 May 18.
10
Glycans as Key Checkpoints of T Cell Activity and Function.糖链作为 T 细胞活性和功能的关键检查点。
Front Immunol. 2018 Nov 27;9:2754. doi: 10.3389/fimmu.2018.02754. eCollection 2018.