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Engineering self-assembled materials to study and direct immune function.
- Source :
-
Advanced drug delivery reviews [Adv Drug Deliv Rev] 2017 May 15; Vol. 114, pp. 60-78. Date of Electronic Publication: 2017 Apr 06. - Publication Year :
- 2017
-
Abstract
- The immune system is an awe-inspiring control structure that maintains a delicate and constantly changing balance between pro-immune functions that fight infection and cancer, regulatory or suppressive functions involved in immune tolerance, and homeostatic resting states. These activities are determined by integrating signals in space and time; thus, improving control over the densities, combinations, and durations with which immune signals are delivered is a central goal to better combat infectious disease, cancer, and autoimmunity. Self-assembly presents a unique opportunity to synthesize materials with well-defined compositions and controlled physical arrangement of molecular building blocks. This review highlights strategies exploiting these capabilities to improve the understanding of how precisely-displayed cues interact with immune cells and tissues. We present work centered on fundamental properties that regulate the nature and magnitude of immune response, highlight pre-clinical and clinical applications of self-assembled technologies in vaccines, cancer, and autoimmunity, and describe some of the key manufacturing and regulatory hurdles facing these areas.<br /> (Copyright © 2017 The Authors. Published by Elsevier B.V. All rights reserved.)
- Subjects :
- Animals
Autoimmunity drug effects
Autoimmunity immunology
Biocompatible Materials therapeutic use
Humans
Immunotherapy
Neoplasms immunology
Neoplasms therapy
Vaccines immunology
Biocompatible Materials chemistry
Biocompatible Materials pharmacology
Bioengineering
Immunity drug effects
Immunity immunology
Subjects
Details
- Language :
- English
- ISSN :
- 1872-8294
- Volume :
- 114
- Database :
- MEDLINE
- Journal :
- Advanced drug delivery reviews
- Publication Type :
- Academic Journal
- Accession number :
- 28392305
- Full Text :
- https://doi.org/10.1016/j.addr.2017.03.005