Engineering New Approaches to Cancer Vaccines

available in PMC 2016 August 01

Bibliographic Details
Main Authors: Irvine, D. J., Mehta, Naveen, Moynihan, Kelly Dare
Other Authors: Massachusetts Institute of Technology. Department of Biological Engineering
Format: Article
Language:en_US
Published: American Association for Cancer Research (AACR) 2017
Online Access:http://hdl.handle.net/1721.1/108488
https://orcid.org/0000-0003-3480-6750
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author Irvine, D. J.
Mehta, Naveen
Moynihan, Kelly Dare
author2 Massachusetts Institute of Technology. Department of Biological Engineering
author_facet Massachusetts Institute of Technology. Department of Biological Engineering
Irvine, D. J.
Mehta, Naveen
Moynihan, Kelly Dare
author_sort Irvine, D. J.
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spelling mit-1721.1/1084882022-10-03T09:28:13Z Engineering New Approaches to Cancer Vaccines Irvine, D. J. Mehta, Naveen Moynihan, Kelly Dare Massachusetts Institute of Technology. Department of Biological Engineering Massachusetts Institute of Technology. Department of Materials Science and Engineering Koch Institute for Integrative Cancer Research at MIT Mehta, Naveen Moynihan, Kelly Dare available in PMC 2016 August 01 Recently, a number of promising approaches have been developed using synthetic chemistry, materials science, and bioengineering-based strategies to address challenges in the design of more effective cancer vaccines. At the stage of initial priming, potency can be improved by maximizing vaccine delivery to lymph nodes. Because lymphatic uptake from peripheral tissues is strongly size dependent, antigens and adjuvants packaged into optimally sized nanoparticles access the lymph node with much greater efficiency than unformulated vaccines. Once primed, T cells must home to the tumor site. Because T cells acquire the necessary surface receptors in the local lymph node draining the tissue of interest, vaccines must be engineered that reach organs, such as the lung and gut, which are common sites of tumor lesions but inaccessible by traditional vaccination routes. Particulate vaccine carriers can improve antigen exposure in these organs, resulting in greater lymphocyte priming. Immunomodulatory agents can also be injected directly into the tumor site to stimulate a systemic response capable of clearing even distal lesions; materials have been designed that entrap or slowly release immunomodulators at the tumor site, reducing systemic exposure and improving therapeutic efficacy. Finally, lessons learned from the design of biomaterial-based scaffolds in regenerative medicine have led to the development of implantable vaccines that recruit and activate antigen-presenting cells to drive antitumor immunity. Overall, these engineering strategies represent an expanding toolkit to create safe and effective cancer vaccines. United States. National Institutes of Health (CA174795) United States. National Institutes of Health (CA172164) 2017-04-28T14:42:51Z 2017-04-28T14:42:51Z 2015-08 Article http://purl.org/eprint/type/JournalArticle 2326-6066 2326-6074 http://hdl.handle.net/1721.1/108488 Mehta, Naveen K., Kelly D. Moynihan, and Darrell J. Irvine. “Engineering New Approaches to Cancer Vaccines.” Cancer Immunology Research 3, no. 8 (July 8, 2015): 836–843. https://orcid.org/0000-0003-3480-6750 en_US http://dx.doi.org/10.1158/2326-6066.cir-15-0112 Cancer Immunology Research Creative Commons Attribution-Noncommercial-Share Alike http://creativecommons.org/licenses/by-nc-sa/4.0/ application/pdf American Association for Cancer Research (AACR) PMC
spellingShingle Irvine, D. J.
Mehta, Naveen
Moynihan, Kelly Dare
Engineering New Approaches to Cancer Vaccines
title Engineering New Approaches to Cancer Vaccines
title_full Engineering New Approaches to Cancer Vaccines
title_fullStr Engineering New Approaches to Cancer Vaccines
title_full_unstemmed Engineering New Approaches to Cancer Vaccines
title_short Engineering New Approaches to Cancer Vaccines
title_sort engineering new approaches to cancer vaccines
url http://hdl.handle.net/1721.1/108488
https://orcid.org/0000-0003-3480-6750
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