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Author Notes:

Susan N. Thomas, susan.thomas@gatech.edu

The authors report no financial or personal conflict of interest relevant to this manuscript.

Subject:

Research Funding:

This work was supported by National Institutes of Health (NIH) Grants R01CA207619, R01CA247484, U01CA214354, and the Shurl and Kay Curci Foundation.

Keywords:

  • Science & Technology
  • Life Sciences & Biomedicine
  • Immunology
  • Nanotechnology
  • Nanoparticle
  • Lymph node drug delivery
  • Targeted delivery
  • Controlled release
  • SUBCAPSULAR SINUS MACROPHAGES
  • ANTIGEN-PRESENTING CELLS
  • POLY(PROPYLENE SULFIDE) NANOPARTICLES
  • SYNTHETIC VACCINE NANOPARTICLES
  • IRON-OXIDE NANOPARTICLES
  • HIGH ENDOTHELIAL VENULES
  • DRUG-DELIVERY SYSTEMS
  • NATURAL-KILLER-CELLS
  • IN-VIVO
  • DENDRITIC CELLS

Innovations in lymph node targeting nanocarriers

Tools:

Journal Title:

SEMINARS IN IMMUNOLOGY

Volume:

Volume 56

Publisher:

, Pages 101534-101534

Type of Work:

Article | Post-print: After Peer Review

Abstract:

Lymph nodes are secondary lymphoid tissues in the body that facilitate the co-mingling of immune cells to enable and regulate the adaptive immune response. They are also tissues implicated in a variety of diseases, including but not limited to malignancy. The ability to access lymph nodes is thus attractive for a variety of therapeutic and diagnostic applications. As nanotechnologies are now well established for their potential in translational biomedical applications, their high relevance to applications that involve lymph nodes is highlighted. Herein, established paradigms of nanocarrier design to enable delivery to lymph nodes are discussed, considering the unique lymph node tissue structure as well as lymphatic system physiology. The influence of delivery mechanism on how nanocarrier systems distribute to different compartments and cells that reside within lymph nodes is also elaborated. Finally, current advanced nanoparticle technologies that have been developed to enable lymph node delivery are discussed.

Copyright information:

This is an Open Access work distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (https://creativecommons.org/licenses/by-nc-nd/4.0/).
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