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Author Notes:

Susan N. Thomas, Ph.D., George W. Woodruff School of Mechanical Engineering, Georgia Institute of Technology, 315 Ferst Drive NW, Atlanta, GA 30332, Tel: +1 (404) 385-1126, Fax: +1 (404) 385-1397,Email: susan.thomas@gatech.edu

Subject:

Research Funding:

This work was supported by National Institutes of Health (NIH) Grants R01CA207619 and R01CA247484, Department of Defense Grant CA150523, and the Curci Foundation. M.P.M. was supported by a National Science Foundation Graduate Research Fellowship.

Keywords:

  • drug delivery system
  • controlled release
  • tumor immunotherapy
  • immunoengineering
  • lymph node
  • lymphatics

Lymphatic immunomodulation using engineered drug delivery systems for cancer immunotherapy

Tools:

Journal Title:

ADVANCED DRUG DELIVERY REVIEWS

Volume:

Volume 160

Publisher:

, Pages 19-35

Type of Work:

Article | Post-print: After Peer Review

Abstract:

Though immunotherapy has revolutionized the treatment of cancer to improve disease outcomes, an array of challenges remain that limit wider clinical success, including low rate of response and immune-related adverse events. Targeting immunomodulatory drugs to therapeutically relevant tissues offers a way to overcome these challenges by potentially enabling enhanced therapeutic efficacy and decreased incidence of side effects. Research highlighting the importance of lymphatic tissues in the response to immunotherapy has increased interest in the application of engineered drug delivery systems (DDSs) to enable specific targeting of immunomodulators to lymphatic tissues and cells that they house. To this end, a variety of DDS platforms have been developed that enable more efficient uptake into lymphatic vessels and lymph nodes to provide targeted modulation of the immune response to cancer. This can occur either by delivery of immunotherapeutics to lymphatics tissues or by direct modulation of the lymphatic vasculature itself due to their direct involvement in tumor immune processes. This review will highlight DDS platforms that, by enabling the activities of cancer vaccines, chemotherapeutics, immune checkpoint blockade (ICB) antibodies, and anti- or pro-lymphangiogenic factors to lymphatic tissues through directed delivery and controlled release, augment cancer immunotherapy.

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/rdf).
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