Embracing nanomaterials' interactions with the innate immune system

Abraham J.P. Teunissen (Corresponding author), Marianne E. Burnett, Geoffrey Prévot, Emma D. Klein, Daniel Bivona, Willem J.M. Mulder (Corresponding author)

Research output: Contribution to journalReview articlepeer-review

12 Citations (Scopus)
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Abstract

Immunotherapy has firmly established itself as a compelling avenue for treating disease. Although many clinically approved immunotherapeutics engage the adaptive immune system, therapeutically targeting the innate immune system remains much less explored. Nanomedicine offers a compelling opportunity for innate immune system engagement, as many nanomaterials inherently interact with myeloid cells (e.g., monocytes, macrophages, neutrophils, and dendritic cells) or can be functionalized to target their cell-surface receptors. Here, we provide a perspective on exploiting nanomaterials for innate immune system regulation. We focus on specific nanomaterial design parameters, including size, form, rigidity, charge, and surface decoration. Furthermore, we examine the potential of high-throughput screening and machine learning, while also providing recommendations for advancing the field. This article is categorized under: Nanotechnology Approaches to Biology > Nanoscale Systems in Biology Diagnostic Tools > In Vivo Nanodiagnostics and Imaging Therapeutic Approaches and Drug Discovery > Nanomedicine for Oncologic Disease.

Original languageEnglish
Article numbere1719
Number of pages22
JournalWiley Interdisciplinary Reviews: Nanomedicine and Nanobiotechnology
Volume13
Issue number6
Early online date13 Apr 2021
DOIs
Publication statusPublished - Nov 2021

Bibliographical note

Funding Information:
The authors thank the Icahn School of Medicine at Mount Sinai. This work was supported by the National Institutes of Health (NIH) grants R01 CA220234, R01 HL144072, P01 HL131478, and NWO/ZonMW Vici 91818622 (W.J.M.M.).

Publisher Copyright:
© 2021 Wiley Periodicals LLC.

Copyright:
Copyright 2021 Elsevier B.V., All rights reserved.

Funding

The authors thank the Icahn School of Medicine at Mount Sinai. This work was supported by the National Institutes of Health (NIH) grants R01 CA220234, R01 HL144072, P01 HL131478, and NWO/ZonMW Vici 91818622 (W.J.M.M.). The authors thank the Icahn School of Medicine at Mount Sinai. This work was supported by the National Institutes of Health (NIH) grants R01 CA220234, R01 HL144072, P01 HL131478, and NWO/ZonMW Vici 91818622 (W.J.M.M.).

FundersFunder number
ZonMw : Dutch Organisation for Health Research and Development91818622
National Institutes of Health
National Heart, Lung, and Blood InstituteR01HL144072, P01HL131478
National Cancer InstituteR01CA220234
Icahn School of Medicine at Mount Sinai
Nederlandse Organisatie voor Wetenschappelijk Onderzoek

    Keywords

    • innate immunotherapy
    • nanomaterials
    • nanomedicine
    • nanotherapeutics

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