4.8 Review

Leveraging self-assembled nanobiomaterials for improved cancer immunotherapy

Journal

CANCER CELL
Volume 40, Issue 3, Pages 255-276

Publisher

CELL PRESS
DOI: 10.1016/j.ccell.2022.01.006

Keywords

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Funding

  1. Ryan Fellowship
  2. International Institute for Nanotechnology at Northwestern University
  3. Northwestern University Multidisciplinary Visual Sciences Training Program - National Eye Institute (NEI) [2T32EY025202-06]
  4. Director's New Innovator Award [1DP2HL132390-01]
  5. National Science Foundation [CBET-1806007, 1453576]
  6. Div Of Chem, Bioeng, Env, & Transp Sys
  7. Directorate For Engineering [1453576] Funding Source: National Science Foundation

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Nanotechnologies applied to cancer immunotherapy focus on self-assembling drug delivery systems composed of lipids and/or polymers, which improve the therapeutic index of drugs and allow for better control of their pharmacokinetics, biodistribution, and bioavailability. This article discusses the fundamental design, suitability, and inherent properties of nanomaterials that induce anti-tumor immune responses and support anti-cancer vaccination. It also presents various targeting strategies and highlights how nanocarrier structure and surface chemistry can be utilized for controlled delivery to the tumor microenvironment while minimizing off-target effects.
Nanomaterials and targeted drug delivery vehicles improve the therapeutic index of drugs and permit greater control over their pharmacokinetics, biodistribution, and bioavailability. Here, nanotechnologies applied to cancer immunotherapy are discussed with a focus on current and next generation self-assembling drug delivery systems composed of lipids and/or polymers. Topics covered include the fundamental design, suitability, and inherent properties of nanomaterials that induce anti-tumor immune responses and support anti-cancer vaccination. Established active and passive targeting strategies as well as newer indirectmethods are presented together with insights into how nanocarrier structure and surface chemistry can be leveraged for controlled delivery to the tumor microenvironment while minimizing off-target effects.

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