Engineering Targeting Materials for Therapeutic Cancer Vaccines.

cancer immunoengineering immunotherapy material engineering targeting strategies vaccines

Journal

Frontiers in bioengineering and biotechnology
ISSN: 2296-4185
Titre abrégé: Front Bioeng Biotechnol
Pays: Switzerland
ID NLM: 101632513

Informations de publication

Date de publication:
2020
Historique:
received: 10 10 2019
accepted: 10 01 2020
entrez: 3 3 2020
pubmed: 3 3 2020
medline: 3 3 2020
Statut: epublish

Résumé

Therapeutic cancer vaccines constitute a valuable tool to educate the immune system to fight tumors and prevent cancer relapse. Nevertheless, the number of cancer vaccines in the clinic remains very limited to date, highlighting the need for further technology development. Recently, cancer vaccines have been improved by the use of materials, which can strongly enhance their intrinsic properties and biodistribution profile. Moreover, vaccine efficacy and safety can be substantially modulated through selection of the site at which they are delivered, which fosters the engineering of materials capable of targeting cancer vaccines to specific relevant sites, such as within the tumor or within lymphoid organs, to further optimize their immunotherapeutic effects. In this review, we aim to give the reader an overview of principles and current strategies to engineer therapeutic cancer vaccines, with a particular focus on the use of site-specific targeting materials. We will first recall the goal of therapeutic cancer vaccination and the type of immune responses sought upon vaccination, before detailing key components of cancer vaccines. We will then present how materials can be engineered to enhance the vaccine's pharmacokinetic and pharmacodynamic properties. Finally, we will discuss the rationale for site-specific targeting of cancer vaccines and provide examples of current targeting technologies.

Identifiants

pubmed: 32117911
doi: 10.3389/fbioe.2020.00019
pmc: PMC7026271
doi:

Types de publication

Journal Article Review

Langues

eng

Pagination

19

Subventions

Organisme : NCI NIH HHS
ID : R01 CA219304
Pays : United States
Organisme : NCI NIH HHS
ID : R01 CA253248
Pays : United States

Informations de copyright

Copyright © 2020 Briquez, Hauert, de Titta, Gray, Alpar, Swartz and Hubbell.

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Auteurs

Priscilla S Briquez (PS)

Pritzker School of Molecular Engineering, The University of Chicago, Chicago, IL, United States.

Sylvie Hauert (S)

Pritzker School of Molecular Engineering, The University of Chicago, Chicago, IL, United States.

Alexandre de Titta (A)

Agap2 Zürich, Zurich, Switzerland.

Laura T Gray (LT)

Pritzker School of Molecular Engineering, The University of Chicago, Chicago, IL, United States.

Aaron T Alpar (AT)

Pritzker School of Molecular Engineering, The University of Chicago, Chicago, IL, United States.

Melody A Swartz (MA)

Pritzker School of Molecular Engineering, The University of Chicago, Chicago, IL, United States.
Ben May Department of Cancer Research, The University of Chicago, Chicago, IL, United States.
Committee on Immunology, The University of Chicago, Chicago, IL, United States.

Jeffrey A Hubbell (JA)

Pritzker School of Molecular Engineering, The University of Chicago, Chicago, IL, United States.
Committee on Immunology, The University of Chicago, Chicago, IL, United States.

Classifications MeSH