• 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

利用生物材料构建淋巴结微环境以实现免疫或免疫耐受。

Harnessing biomaterials to engineer the lymph node microenvironment for immunity or tolerance.

作者信息

Andorko James I, Hess Krystina L, Jewell Christopher M

机构信息

Fischell Department of Bioengineering, University of Maryland, 2212 Jeong H. Kim Engineering Building, College Park, Maryland, 20742, USA.

出版信息

AAPS J. 2015 Mar;17(2):323-38. doi: 10.1208/s12248-014-9708-2. Epub 2014 Dec 23.

DOI:10.1208/s12248-014-9708-2
PMID:25533221
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4365095/
Abstract

Nanoparticles, microparticles, and other biomaterials are advantageous in vaccination because these materials provide opportunities to modulate specific characteristics of immune responses. This idea of "tuning" immune responses has recently been used to combat infectious diseases and cancer, and to induce tolerance during organ transplants or autoimmune disease. Lymph nodes and other secondary lymphoid organs such as the spleen play crucial roles in determining if and how these responses develop following vaccination or immunotherapy. Thus, by manipulating the local microenvironments within these immunological command centers, the nature of systemic immune response can be controlled. This review provides recent examples that harness the interactions between biomaterials and lymph nodes or other secondary lymphoid organs to generate immunity or promote tolerance. These strategies draw on mechanical properties, surface chemistry, stability, and targeting to alter the interactions of cells, signals, and vaccine components in lymph nodes. While there are still many unanswered questions surrounding how best to design biomaterial-based vaccines to promote specific structures or functions in lymph nodes, features such as controlled release and targeting will help pave the way for the next generation of vaccines and immunotherapies that generate immune responses tuned for specific applications.

摘要

纳米颗粒、微粒及其他生物材料在疫苗接种中具有优势,因为这些材料为调节免疫反应的特定特性提供了机会。这种“调节”免疫反应的理念最近已被用于对抗传染病和癌症,以及在器官移植或自身免疫性疾病期间诱导免疫耐受。淋巴结及其他二级淋巴器官(如脾脏)在决定接种疫苗或进行免疫治疗后这些反应是否以及如何发展方面起着关键作用。因此,通过操纵这些免疫指挥中心内的局部微环境,可以控制全身免疫反应的性质。本综述提供了近期的实例,这些实例利用生物材料与淋巴结或其他二级淋巴器官之间的相互作用来产生免疫或促进免疫耐受。这些策略利用机械性能、表面化学、稳定性和靶向性来改变淋巴结中细胞、信号和疫苗成分之间的相互作用。虽然围绕如何最佳设计基于生物材料的疫苗以促进淋巴结中的特定结构或功能仍有许多未解答的问题,但诸如控释和靶向等特性将有助于为下一代能产生针对特定应用进行调节的免疫反应的疫苗和免疫疗法铺平道路。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0252/4365095/f47c6fc45de8/12248_2014_9708_Fig9_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0252/4365095/78a27abb5546/12248_2014_9708_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0252/4365095/6902b45e99f2/12248_2014_9708_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0252/4365095/fd0b02f84661/12248_2014_9708_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0252/4365095/cd69e0373f2d/12248_2014_9708_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0252/4365095/958c5620eb79/12248_2014_9708_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0252/4365095/0889598b1d75/12248_2014_9708_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0252/4365095/688cc532c060/12248_2014_9708_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0252/4365095/61c11b007bfb/12248_2014_9708_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0252/4365095/f47c6fc45de8/12248_2014_9708_Fig9_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0252/4365095/78a27abb5546/12248_2014_9708_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0252/4365095/6902b45e99f2/12248_2014_9708_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0252/4365095/fd0b02f84661/12248_2014_9708_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0252/4365095/cd69e0373f2d/12248_2014_9708_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0252/4365095/958c5620eb79/12248_2014_9708_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0252/4365095/0889598b1d75/12248_2014_9708_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0252/4365095/688cc532c060/12248_2014_9708_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0252/4365095/61c11b007bfb/12248_2014_9708_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0252/4365095/f47c6fc45de8/12248_2014_9708_Fig9_HTML.jpg

相似文献

1
Harnessing biomaterials to engineer the lymph node microenvironment for immunity or tolerance.利用生物材料构建淋巴结微环境以实现免疫或免疫耐受。
AAPS J. 2015 Mar;17(2):323-38. doi: 10.1208/s12248-014-9708-2. Epub 2014 Dec 23.
2
Emerging skin-targeted drug delivery strategies to engineer immunity: A focus on infectious diseases.新兴的皮肤靶向药物传递策略在免疫工程中的应用:关注传染病。
Expert Opin Drug Deliv. 2021 Feb;18(2):151-167. doi: 10.1080/17425247.2021.1823964. Epub 2020 Oct 6.
3
Engineering Strategies for Lymph Node Targeted Immune Activation.淋巴结靶向免疫激活的工程策略
Acc Chem Res. 2020 Oct 20;53(10):2055-2067. doi: 10.1021/acs.accounts.0c00260. Epub 2020 Sep 10.
4
Role of lymph node stroma and microenvironment in T cell tolerance.淋巴结基质和微环境在 T 细胞耐受中的作用。
Immunol Rev. 2019 Nov;292(1):9-23. doi: 10.1111/imr.12799. Epub 2019 Sep 19.
5
Lymph node targeting strategies to improve vaccination efficacy.淋巴节点靶向策略以提高疫苗效力。
J Control Release. 2017 Dec 10;267:47-56. doi: 10.1016/j.jconrel.2017.08.009. Epub 2017 Aug 15.
6
Engineering immunity: Modulating dendritic cell subsets and lymph node response to direct immune-polarization and vaccine efficacy.工程化免疫:调节树突状细胞亚群及淋巴结反应以实现直接免疫极化和疫苗效力
J Control Release. 2015 Dec 10;219:610-621. doi: 10.1016/j.jconrel.2015.09.063. Epub 2015 Oct 20.
7
Engineering vaccines and niches for immune modulation.设计用于免疫调节的疫苗和生态位。
Acta Biomater. 2014 Apr;10(4):1728-40. doi: 10.1016/j.actbio.2013.12.036. Epub 2013 Dec 27.
8
Cell and tissue engineering in lymph nodes for cancer immunotherapy.淋巴结中的细胞和组织工程用于癌症免疫治疗。
Adv Drug Deliv Rev. 2020;161-162:42-62. doi: 10.1016/j.addr.2020.07.023. Epub 2020 Aug 1.
9
Targeting dendritic cells with biomaterials: developing the next generation of vaccines.利用生物材料靶向树突状细胞:开发新一代疫苗。
Trends Immunol. 2006 Dec;27(12):573-9. doi: 10.1016/j.it.2006.10.005. Epub 2006 Oct 16.
10
Harnessing the lymph node microenvironment.利用淋巴结微环境。
Curr Opin Organ Transplant. 2018 Feb;23(1):73-82. doi: 10.1097/MOT.0000000000000488.

引用本文的文献

1
Tailoring biomaterials for vaccine delivery.为疫苗传递量身定制生物材料。
J Nanobiotechnology. 2024 Aug 12;22(1):480. doi: 10.1186/s12951-024-02758-0.
2
Unlocking Transplant Tolerance with Biomaterials.利用生物材料实现移植耐受
Adv Healthc Mater. 2025 Feb;14(5):e2400965. doi: 10.1002/adhm.202400965. Epub 2024 Jul 3.
3
Leveraging Lymphatic System Targeting in Systemic Lupus Erythematosus for Improved Clinical Outcomes.利用淋巴系统靶向治疗红斑狼疮以改善临床疗效。

本文引用的文献

1
Nanoparticle delivery of donor antigens for transplant tolerance in allogeneic islet transplantation.纳米颗粒递送供体抗原用于同种异体胰岛移植中的移植耐受
Biomaterials. 2014 Oct;35(31):8887-8894. doi: 10.1016/j.biomaterials.2014.06.044. Epub 2014 Jul 25.
2
Designing and building the next generation of improved vaccine adjuvants.设计和构建新一代改良疫苗佐剂。
J Control Release. 2014 Sep 28;190:563-79. doi: 10.1016/j.jconrel.2014.06.027. Epub 2014 Jul 3.
3
Enhancing efficacy of anticancer vaccines by targeted delivery to tumor-draining lymph nodes.
Pharmacol Rev. 2024 Feb 13;76(2):228-250. doi: 10.1124/pharmrev.123.000938.
4
Dissecting regulatory T cell expansion using polymer microparticles presenting defined ratios of self-antigen and regulatory cues.利用呈现特定比例自身抗原和调节信号的聚合物微粒剖析调节性T细胞的扩增。
Front Bioeng Biotechnol. 2023 Jun 27;11:1184938. doi: 10.3389/fbioe.2023.1184938. eCollection 2023.
5
Delivery of costimulatory blockade to lymph nodes promotes transplant acceptance in mice.共刺激阻断剂递送至淋巴结可促进小鼠移植耐受。
J Clin Invest. 2022 Dec 15;132(24):e159672. doi: 10.1172/JCI159672.
6
Self-Assembly of Immune Signals to Program Innate Immunity through Rational Adjuvant Design.通过合理的佐剂设计实现免疫信号的自组装以编程固有免疫。
Adv Sci (Weinh). 2022 Nov 14;10(1):e2202393. doi: 10.1002/advs.202202393.
7
Spatial delivery of immune cues to lymph nodes to define therapeutic outcomes in cancer vaccination.将免疫信号递送至淋巴结的空间分布,以确定癌症疫苗接种的治疗效果。
Biomater Sci. 2022 Aug 9;10(16):4612-4626. doi: 10.1039/d2bm00403h.
8
Integrative lymph node-mimicking models created with biomaterials and computational tools to study the immune system.利用生物材料和计算工具创建的综合淋巴结模拟模型,用于研究免疫系统。
Mater Today Bio. 2022 Apr 21;14:100269. doi: 10.1016/j.mtbio.2022.100269. eCollection 2022 Mar.
9
Albumin nanoparticle containing a PI3Kγ inhibitor and paclitaxel in combination with α-PD1 induces tumor remission of breast cancer in mice.载有 PI3Kγ 抑制剂和紫杉醇的白蛋白纳米颗粒与 α-PD1 联合应用可诱导小鼠乳腺癌肿瘤消退。
Sci Transl Med. 2022 May 4;14(643):eabl3649. doi: 10.1126/scitranslmed.abl3649.
10
Mapping the Mechanical and Immunological Profiles of Polymeric Microneedles to Enable Vaccine and Immunotherapy Applications.绘制聚合物微针的机械和免疫特性图谱,以实现疫苗和免疫治疗应用。
Front Immunol. 2022 Mar 14;13:843355. doi: 10.3389/fimmu.2022.843355. eCollection 2022.
通过靶向递送至肿瘤引流淋巴结来提高抗癌疫苗的疗效。
Cancer Immunol Res. 2014 May;2(5):436-47. doi: 10.1158/2326-6066.CIR-14-0019-T. Epub 2014 Feb 11.
4
Combinatorial delivery of immunosuppressive factors to dendritic cells using dual-sized microspheres.使用双尺寸微球将免疫抑制因子组合递送至树突状细胞。
J Mater Chem B. 2014 May 7;2(17):2562-2574. doi: 10.1039/C3TB21460E.
5
Laminins affect T cell trafficking and allograft fate.层粘连蛋白影响 T 细胞迁移和移植物命运。
J Clin Invest. 2014 May;124(5):2204-18. doi: 10.1172/JCI73683. Epub 2014 Apr 1.
6
Emerging roles of lymphatic endothelium in regulating adaptive immunity.淋巴管内皮细胞在调节适应性免疫中的新作用。
J Clin Invest. 2014 Mar;124(3):943-52. doi: 10.1172/JCI73316. Epub 2014 Mar 3.
7
A biodegradable nanoparticle platform for the induction of antigen-specific immune tolerance for treatment of autoimmune disease.一种用于诱导抗原特异性免疫耐受以治疗自身免疫性疾病的可生物降解纳米颗粒平台。
ACS Nano. 2014 Mar 25;8(3):2148-60. doi: 10.1021/nn405033r. Epub 2014 Feb 27.
8
Structure-based programming of lymph-node targeting in molecular vaccines.基于结构的分子疫苗中淋巴结靶向编程。
Nature. 2014 Mar 27;507(7493):519-22. doi: 10.1038/nature12978. Epub 2014 Feb 16.
9
Treatment of experimental autoimmune encephalomyelitis by codelivery of disease associated Peptide and dexamethasone in acetalated dextran microparticles.通过在缩醛化葡聚糖微粒中共递送疾病相关肽和地塞米松治疗实验性自身免疫性脑脊髓炎
Mol Pharm. 2014 Mar 3;11(3):828-35. doi: 10.1021/mp4005172. Epub 2014 Feb 4.
10
Therapeutic inflammatory monocyte modulation using immune-modifying microparticles.免疫调节微颗粒治疗炎症性单核细胞调节。
Sci Transl Med. 2014 Jan 15;6(219):219ra7. doi: 10.1126/scitranslmed.3007563.