Impact of nanoparticle properties on immune cell interactions in the lymph node
- PMID: 39701340
- DOI: 10.1016/j.actbio.2024.12.039
Impact of nanoparticle properties on immune cell interactions in the lymph node
Abstract
The lymphatic system plays an important role in health and many diseases, such as cancer, autoimmune, cardiovascular, metabolic, hepatic, viral, and other infectious diseases. The lymphatic system is, therefore, an important treatment target site for a range of diseases. Lymph nodes (LNs), rich in T cells, B cells, dendritic cells, and macrophages, are also primary sites of action for vaccines and immunotherapies. Promoting the delivery of therapeutics and vaccines to LNs can, therefore, enhance treatment efficacy and facilitate avoidance of off-target side effects by enabling a reduction in therapeutic dose. Several nanoparticle (NP) based delivery systems, such as polymeric NPs, lipid NPs, liposomes, micelles, and dendrimers, have been reported to enhance the delivery of therapeutics and/or vaccines to LNs. Specific uptake into the lymph following injection into tissues is highly dependent on particle properties, particularly particle size, as small molecules are more likely to be taken up by blood capillaries due to higher blood flow rates, whereas larger molecules and NPs can be specifically transported via the lymphatic vessels to LNs as the initial lymphatic capillaries are more permeable than blood capillaries. Once NPs enter LNs, particle properties also have an important influence on their disposition within the node and association with immune cells, which has significant implications for the design of vaccines and immunotherapies. This review article focuses on the impact of NP properties, such as size, surface charge and modification, and route of administration, on lymphatic uptake, retention, and interactions with immune cells in LNs. We suggest that optimizing all these factors can enhance the efficacy of vaccines or therapeutics with targets in the lymphatics and also be helpful for the rational design of vaccines. STATEMENT OF SIGNIFICANCE: The lymphatic system plays an essential role in health and is an important treatment target site for a range of diseases. Promoting the delivery of immunotherapies and vaccines to immune cells in lymph nodes can enhance efficacy and facilitate avoidance of off-target side effects by enabling a reduction in therapeutic dose. One of the major approaches used to deliver therapeutics and vaccines to lymph nodes is via injection in nanoparticle delivery systems. This review aims to provide an overview of the impact of nanoparticle properties, such as size, surface charge, modification, and route of administration, on lymphatic uptake, lymph node retention, and interactions with immune cells in lymph nodes. This will inform the design of future improved nanoparticle systems for vaccines and immunotherapies.
Keywords: Drug delivery; Immune cell; Immunotherapy; Lymph node; Lymphatics; Nanoparticles; Vaccine.
Copyright © 2024 The Authors. Published by Elsevier Inc. All rights reserved.
Conflict of interest statement
Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.
Similar articles
-
Nanoparticles with dense poly(ethylene glycol) coatings with near neutral charge are maximally transported across lymphatics and to the lymph nodes.Acta Biomater. 2022 Jun;145:146-158. doi: 10.1016/j.actbio.2022.03.054. Epub 2022 Apr 2. Acta Biomater. 2022. PMID: 35381399 Free PMC article.
-
Convective diffusion of nanoparticles from the epithelial barrier toward regional lymph nodes.Adv Colloid Interface Sci. 2013 Nov;199-200:23-43. doi: 10.1016/j.cis.2013.06.002. Epub 2013 Jun 10. Adv Colloid Interface Sci. 2013. PMID: 23859221 Free PMC article. Review.
-
Engineering Strategies for Lymph Node Targeted Immune Activation.Acc Chem Res. 2020 Oct 20;53(10):2055-2067. doi: 10.1021/acs.accounts.0c00260. Epub 2020 Sep 10. Acc Chem Res. 2020. PMID: 32910636
-
High-Density Lipoprotein Composition Influences Lymphatic Transport after Subcutaneous Administration.Mol Pharm. 2020 Aug 3;17(8):2938-2951. doi: 10.1021/acs.molpharmaceut.0c00348. Epub 2020 Jul 13. Mol Pharm. 2020. PMID: 32543863
-
Lymphatic distribution considerations for subunit vaccine design and development.Vaccine. 2024 Apr 11;42(10):2519-2529. doi: 10.1016/j.vaccine.2024.03.033. Epub 2024 Mar 16. Vaccine. 2024. PMID: 38494411 Review.
Cited by
-
Next-Generation Vaccine Platforms: Integrating Synthetic Biology, Nanotechnology, and Systems Immunology for Improved Immunogenicity.Vaccines (Basel). 2025 May 30;13(6):588. doi: 10.3390/vaccines13060588. Vaccines (Basel). 2025. PMID: 40573919 Free PMC article. Review.
-
M72 Fusion Proteins in Nanocapsules Enhance BCG Efficacy Against Bovine Tuberculosis in a Mouse Model.Pathogens. 2025 Jun 16;14(6):592. doi: 10.3390/pathogens14060592. Pathogens. 2025. PMID: 40559600 Free PMC article.
-
Evaluation of oral and injectable liposome-based vaccines with synthesized lipid for Japanese encephalitis virus in Sprague-Dawley rats.Clin Exp Vaccine Res. 2025 Jul;14(3):276-288. doi: 10.7774/cevr.2025.14.e28. Epub 2025 Jun 17. Clin Exp Vaccine Res. 2025. PMID: 40741064 Free PMC article.
References
Publication types
MeSH terms
LinkOut - more resources
Full Text Sources
Research Materials
Miscellaneous