Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2018 Nov 14;18(11):6655-6659.
doi: 10.1021/acs.nanolett.8b02340. Epub 2018 Sep 10.

Immunomodulating Nanomedicine for Cancer Therapy

Affiliations
Review

Immunomodulating Nanomedicine for Cancer Therapy

Zhigang Liu et al. Nano Lett. .

Abstract

Nanomaterials offer unique advantages as drug-delivery vehicles for cancer therapeutics. For immuno-oncology applications, cancer nanomedicine should be developed beyond drug-delivery platforms. A greater emphasis on actively modulating host anticancer immunity using nanomaterials provides new avenues for developing novel cancer therapeutics.

Keywords: Nanomedicine; cancer immunotherapy; cancer vaccine; drug delivery; nanotechnology.

PubMed Disclaimer

Conflict of interest statement

The authors declare no competing financial interest.

Figures

Figure 1
Figure 1
Examples of nanomedicine strategies to enhance antitumor immune responses. (a) Lipid-based nanoparticles encapsulated with nucleic acids such as RNA encoding for mutant antigens can be designed to home to professional antigen-presenting cells (APCs) such as dendritic cells (DCs). The translation and cross-presentation of the mutant antigens by DCs then primes antitumor memory T cell responses. (b) Nanomedicine can also help improve the efficacy of cancer vaccines. Synthetic high-density lipoprotein (sHDL) nanoparticles decorated with tumor antigens can promote the more-efficient delivery to APCs in lymphoid tissues, resulting in improved DC maturation and T cell-mediated tumor killing. (c) Beyond delivery, nanoparticles themselves can also promote antitumor immune cell phenotypes. Iron oxide nanoparticles, for example, can polarize tumor-associated macrophages from a protumor M2-like to an antitumor M1-like phenotype, which releases reactive oxygen species (ROS) to induce tumor cell killing.

References

    1. Mellman I.; Coukos G.; Dranoff G. Cancer immunotherapy comes of age. Nature 2011, 480, 480–489. 10.1038/nature10673. - DOI - PMC - PubMed
    1. Kvistborg P.; Yewdell J. W. Enhancing responses to cancer immunotherapy. Science 2018, 359, 516–517. 10.1126/science.aar6574. - DOI - PubMed
    1. Jiang W.; von Roemeling C. A.; Chen Y.; Qie Y.; Liu X.; Chen J.; Kim B. Y. S. Designing nanomedicine for immuno-oncology. Nat. Biomed. Eng. 2017, 1, 0029.10.1038/s41551-017-0029. - DOI
    1. Blanco E.; Shen H.; Ferrari M. Principles of nanoparticle design for overcoming biological barriers to drug delivery. Nat. Biotechnol. 2015, 33, 941–951. 10.1038/nbt.3330. - DOI - PMC - PubMed
    1. Wilhelm S.; Tavares A. J.; Dai Q.; Ohta S.; Audet J.; Dvorak H. F.; Chan W. C. W. Analysis of nanoparticle delivery to tumours. Nat. Rev. Mater. 2016, 1, 16014.10.1038/natrevmats.2016.14. - DOI

Publication types

LinkOut - more resources