Species differences in opsonization and phagocyte recognition of preclinical poly-2-alkyl-2-oxazoline-coated nanoparticles

Poly(ethylene glycol) (PEG) is widely used in nanomedicine design, but emerging PEG immunogenicity in the general population is of therapeutic concern. As alternative, polyoxazolines are gaining popularity, since "polyoxazolinated" nanoparticles show long-circulating properties comparable to PEGylated nanoparticles in mice. Here, we show species differences in opsonization and differential uptake by monocytes and macrophages of nanoparticles coated with either poly-2-methyl-2-oxazoline or poly-2-ethyl-2-oxazoline. These nanoparticles evade murine opsonization process and phagocytic uptake but porcine ficolin 2 (FCN2), through its S2 binding site, recognizes polyoxazolines, and mediates nanoparticle uptake exclusively by porcine monocytes. In human sera, FCN opsonization is isoform-dependent showing inter-individual variability but both FCN2 and complement opsonization promote nanoparticle uptake by human monocytes. However, nanoparticle uptake by human and porcine macrophages is complement-dependent. These findings advance mechanistic understanding of species differences in innate immune recognition of nanomaterials' molecular patterns, and applicable to the selection and chemical design of polymers for engineering of the next generation of stealth nanoparticles.

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Publication Details

Journal
Nature Communications
Published
2025-03-18
DOI
https://doi.org/10.1038/s41467-025-57648-2
Citations
7
Primary Topic
Surfactants and Colloidal Systems
Type
article
Field-Weighted Citation Impact
6.55

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article

Species differences in opsonization and phagocyte recognition of preclinical poly-2-alkyl-2-oxazoline-coated nanoparticles

Emanuele Papini, Stefano Moro, Alessandra Geffner-Smith, Edmondo Maria Benetti et al.
7 citations
Nature Communications
Surfactants and Colloidal Systems
6.55
article

Species differences in opsonization and phagocyte recognition of preclinical poly-2-alkyl-2-oxazoline-coated nanoparticles

Emanuele Papini, Stefano Moro, Alessandra Geffner-Smith, Edmondo Maria Benetti, Alda Natale, Regina Tavano, Patrizia Polverino de Laureto, Matteo Romio, Giovanni Bolcato, Fabrizio Mancin, Lucía Morillas-Becerril, Luana Palazzi, Giorgio Arrigoni, Ilaria Battisti, Ester Jiménez‐Moreno, Patrizio Coin, S. Moein Moghimi, Francisco Corzana, Eliana Schiavon, Mattia Sturlese, G. Ronzani, R. Gervasutti, M. Morbidelli
article en
7 citations

Abstract

Poly(ethylene glycol) (PEG) is widely used in nanomedicine design, but emerging PEG immunogenicity in the general population is of therapeutic concern. As alternative, polyoxazolines are gaining popularity, since "polyoxazolinated" nanoparticles show long-circulating properties comparable to PEGylated nanoparticles in mice. Here, we show species differences in opsonization and differential uptake by monocytes and macrophages of nanoparticles coated with either poly-2-methyl-2-oxazoline or poly-2-ethyl-2-oxazoline. These nanoparticles evade murine opsonization process and phagocytic uptake but porcine ficolin 2 (FCN2), through its S2 binding site, recognizes polyoxazolines, and mediates nanoparticle uptake exclusively by porcine monocytes. In human sera, FCN opsonization is isoform-dependent showing inter-individual variability but both FCN2 and complement opsonization promote nanoparticle uptake by human monocytes. However, nanoparticle uptake by human and porcine macrophages is complement-dependent. These findings advance mechanistic understanding of species differences in innate immune recognition of nanomaterials' molecular patterns, and applicable to the selection and chemical design of polymers for engineering of the next generation of stealth nanoparticles.

Nature CommunicationsVol. 16(1)
University of Padua (IT), Universidad de La Rioja (ES), Istituto Zooprofilattico Sperimentale delle Venezie (IT), University of Colorado Anschutz Medical Campus (US), Swiss Federal Laboratories for Materials Science and Technology (CH), University of Brescia (IT), Newcastle University (GB)
Università degli Studi di Padova, Horizon 2020 Framework Programme
Zero hunger
Openalex Percentile: Top 4%
Surfactants and Colloidal Systems
6.55
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