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用于靶向淋巴结的基于可生物降解聚合物纳米颗粒的疫苗佐剂

Biodegradable Polymeric Nanoparticles-Based Vaccine Adjuvants for Lymph Nodes Targeting.

作者信息

Gutjahr Alice, Phelip Capucine, Coolen Anne-Line, Monge Claire, Boisgard Anne-Sophie, Paul Stéphane, Verrier Bernard

机构信息

Laboratoire de Biologie Tissulaire et d'Ingénierie Thérapeutique, UMR 5305, Université Lyon 1, CNRS, IBCP, Lyon 69007, France.

InvivoGen, Toulouse 31400, France.

出版信息

Vaccines (Basel). 2016 Oct 12;4(4):34. doi: 10.3390/vaccines4040034.


DOI:10.3390/vaccines4040034
PMID:27754314
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5192354/
Abstract

Vaccines have successfully eradicated a large number of diseases. However, some infectious diseases (such as HIV, or ) keep spreading since there is no vaccine to prevent them. One way to overcome this issue is the development of new adjuvant formulations which are able to induce the appropriate immune response without sacrificing safety. Lymph nodes are the site of lymphocyte priming by antigen-presenting cells and subsequent adaptive immune response, and are a promising target for vaccine formulations. In this review, we describe the properties of different polymer-based (e.g., poly lactic-co-glycolic acid, poly lactic acid …) particulate adjuvants as innovative systems, capable of co-delivering immunopotentiators and antigens. We point out how these nanoparticles enhance the delivery of antigens, and how their physicochemical properties modify their uptake by antigen-presenting cells and their migration into lymph nodes. We describe why polymeric nanoparticles increase the persistence into lymph nodes and promote a mature immune response. We also emphasize how nanodelivery directs the response to a specific antigen and allows the induction of a cytotoxic immune response, essential for the fight against intracellular pathogens or cancer. Finally, we highlight the interest of the association between polymer-based vaccines and immunopotentiators, which can potentiate the effect of the molecule by directing it to the appropriate compartment and reducing its toxicity.

摘要

疫苗已成功根除了大量疾病。然而,一些传染病(如艾滋病毒等)仍在不断传播,因为尚无预防这些疾病的疫苗。克服这一问题的一种方法是开发新的佐剂配方,这种配方能够在不牺牲安全性的前提下诱导适当的免疫反应。淋巴结是抗原呈递细胞启动淋巴细胞并引发后续适应性免疫反应的场所,是疫苗配方的一个有前景的靶点。在本综述中,我们描述了不同的基于聚合物的(如聚乳酸-乙醇酸共聚物、聚乳酸……)颗粒佐剂作为创新系统的特性,这些系统能够共同递送免疫增强剂和抗原。我们指出这些纳米颗粒如何增强抗原的递送,以及它们的物理化学性质如何改变抗原呈递细胞对其的摄取及其向淋巴结的迁移。我们描述了为什么聚合物纳米颗粒会增加在淋巴结中的滞留时间并促进成熟的免疫反应。我们还强调了纳米递送如何引导针对特定抗原的反应并诱导细胞毒性免疫反应,这对于对抗细胞内病原体或癌症至关重要。最后,我们强调了基于聚合物的疫苗与免疫增强剂联合使用的意义,这种联合使用可以通过将分子引导至适当的区室并降低其毒性来增强分子的效果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2660/5192354/6d52846acb19/vaccines-04-00034-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2660/5192354/e7eea95cb227/vaccines-04-00034-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2660/5192354/6d52846acb19/vaccines-04-00034-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2660/5192354/e7eea95cb227/vaccines-04-00034-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2660/5192354/6d52846acb19/vaccines-04-00034-g002.jpg

相似文献

[1]
Biodegradable Polymeric Nanoparticles-Based Vaccine Adjuvants for Lymph Nodes Targeting.

Vaccines (Basel). 2016-10-12

[2]
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Molecules. 2023-6-15

[3]
Modeling the kinetics of lymph node retention and exposure of a cargo protein delivered by biotin-functionalized nanoparticles.

Acta Biomater. 2023-10-15

[4]
PLGA particulate delivery systems for subunit vaccines: Linking particle properties to immunogenicity.

Hum Vaccin Immunother. 2016-4-2

[5]
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J Clin Invest. 2016-3-1

[6]
pH-Responsive Poly(D,L-lactic-co-glycolic acid) Nanoparticles with Rapid Antigen Release Behavior Promote Immune Response.

ACS Nano. 2015-4-24

[7]
Poly(lactic acid)-based particulate systems are promising tools for immune modulation.

Acta Biomater. 2016-11-4

[8]
Particulate formulations for the delivery of poly(I:C) as vaccine adjuvant.

Adv Drug Deliv Rev. 2013-6-7

[9]
Adjuvants and delivery systems based on polymeric nanoparticles for mucosal vaccines.

Int J Pharm. 2019-10-24

[10]
[Development of vaccine adjuvants using polymeric nanoparticles and their potential applications for anti-HIV vaccine].

Yakugaku Zasshi. 2007-2

引用本文的文献

[1]
Cancer Vaccines and Beyond: The Transformative Role of Nanotechnology in Immunotherapy.

Pharmaceutics. 2025-2-7

[2]
Advancements in Nanoparticle-Based Adjuvants for Enhanced Tuberculosis Vaccination: A Review.

Vaccines (Basel). 2024-11-27

[3]
Intra-lymph node crosslinking of antigen-bearing polymers enhances humoral immunity and dendritic cell activation.

Bioeng Transl Med. 2024-7-17

[4]
Engineered Cancer Nanovaccines: A New Frontier in Cancer Therapy.

Nanomicro Lett. 2024-9-30

[5]
Nanotechnology's frontier in combatting infectious and inflammatory diseases: prevention and treatment.

Signal Transduct Target Ther. 2024-2-21

[6]
The quest for nanoparticle-powered vaccines in cancer immunotherapy.

J Nanobiotechnology. 2024-2-14

[7]
Nanoparticles and Antiviral Vaccines.

Vaccines (Basel). 2023-12-27

[8]
Uptake Quantification of Antigen Carried by Nanoparticles and Its Impact on Carrier Adjuvanticity Evaluation.

Vaccines (Basel). 2023-12-26

[9]
Self-Assembling Nanovaccine Fused with Flagellin Enhances Protective Effect against Foot-and-Mouth Disease Virus.

Vaccines (Basel). 2023-11-2

[10]
Non-Invasive Vaccines: Challenges in Formulation and Vaccine Adjuvants.

Pharmaceutics. 2023-8-9

本文引用的文献

[1]
Nanoparticles in the clinic.

Bioeng Transl Med. 2016-6-3

[2]
Triggering Intracellular Receptors for Vaccine Adjuvantation.

Trends Immunol. 2016-7-27

[3]
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Curr Opin Immunol. 2016-7-5

[4]
Dendritic cell maturation and cross-presentation: timing matters!

Immunol Rev. 2016-7

[5]
PLGA nanoparticles modified with a TNFα mimicking peptide, soluble Leishmania antigens and MPLA induce T cell priming in vitro via dendritic cell functional differentiation.

Eur J Pharm Biopharm. 2016-5-25

[6]
The preparation and characterization of PLG nanoparticles with an entrapped synthetic TLR7 agonist and their preclinical evaluation as adjuvant for an adsorbed DTaP vaccine.

Eur J Pharm Biopharm. 2016-5-17

[7]
Artificial bacterial biomimetic nanoparticles synergize pathogen-associated molecular patterns for vaccine efficacy.

Biomaterials. 2016-8

[8]
From Antigen Delivery System to Adjuvanticy: The Board Application of Nanoparticles in Vaccinology.

Vaccines (Basel). 2015-11-5

[9]
In vivo characterization of the physicochemical properties of polymer-linked TLR agonists that enhance vaccine immunogenicity.

Nat Biotechnol. 2015-11

[10]
Functional characterization of biodegradable nanoparticles as antigen delivery system.

J Exp Clin Cancer Res. 2015-10-6

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