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Evolution of nanomedicines for the treatment of autoimmune disease: From vehicles for drug delivery to inducers of bystander immunoregulation

Journal

ADVANCED DRUG DELIVERY REVIEWS
Volume 176, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.addr.2021.113898

Keywords

Autoimmunity; Immunoregulation; Nanomedicine; Immune tolerance

Funding

  1. Canadian Institutes of Health Research (CIHR)
  2. Diabetes Canada
  3. Praespero Foundation
  4. Alberta Diabetes Foundation
  5. Ministerio de Economia y Competitividad of Spain
  6. Generalitat de Catalunya

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In the past two decades, research on nanoparticle/microparticle-based compounds for treating autoimmune diseases has experienced explosive growth. Compounds have been evaluated using a variety of materials with different shapes, sizes, surface chemistries, and structures, incorporating various active pharmaceutical ingredients. These compounds can be categorized into four groups based on their intended mechanisms of action.
Over the last two decades, the nanomedicine field has witnessed an explosive growth of research on the development of nanoparticle/microparticle (NP/MP)-based compounds for the treatment of autoimmune diseases. Studies have evaluated compounds generated with a broad range of materials with different shapes, sizes, surface chemistries and structures. A number of active pharmaceutical ingredients, including immunosuppressants, cytokines, nucleotides, peptides, proteins and immunomodulators of various types have been encapsulated into or incorporated onto the surface of these compounds, either individually or in combination, and delivered to animal models of autoimmune inflammation via different administration routes. These NP/MP-based compounds can be categorized into four different groups based on their intended mechanisms of action. Here, we review the engineering designs, the pharmacodynamic and therapeutic correlates and the disease specificity of nanomedicines belonging to each of these groups. (c) 2021 The Authors. Published by Elsevier B.V. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).

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