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PEGylated Gold Nanoparticles Target Age-Associated B Cells In Vivo

Sandra Hočevar Orcid Logo, Viola Puddinu Orcid Logo, Laetitia Haeni, Alke Petri-Fink Orcid Logo, Julia Wagner, Montserrat Alvarez, Martin Clift Orcid Logo, Carole Bourquin Orcid Logo

ACS Nano, Volume: 16, Issue: 11, Pages: 18119 - 18132

Swansea University Author: Martin Clift Orcid Logo

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Abstract

Engineered gold nanoparticles (GNPs) have become a useful tool in various therapeutic and diagnostic applications. Uncertainty remains regarding the possible impact of GNPs on the immune system. In this regard, we investigated the interactions of polymer-coated GNPs with B cells and their functions...

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Published in: ACS Nano
ISSN: 1936-0851 1936-086X
Published: American Chemical Society (ACS) 2022
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URI: https://cronfa.swan.ac.uk/Record/cronfa61638
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spelling v2 61638 2022-10-24 PEGylated Gold Nanoparticles Target Age-Associated B Cells In Vivo 71bf49b157691e541950f5c3f49c9169 0000-0001-6133-3368 Martin Clift Martin Clift true false 2022-10-24 BMS Engineered gold nanoparticles (GNPs) have become a useful tool in various therapeutic and diagnostic applications. Uncertainty remains regarding the possible impact of GNPs on the immune system. In this regard, we investigated the interactions of polymer-coated GNPs with B cells and their functions in mice. Surprisingly, we observed that polymer-coated GNPs mainly interact with the recently identified subpopulation of B lymphocytes named age-associated B cells (ABCs). Importantly, we also showed that GNPs did not affect cell viability or the percentages of other B cell populations in different organs. Furthermore, GNPs did not activate B cell innate-like immune responses in any of the tested conditions, nor did they impair adaptive B cell responses in immunized mice. Together, these data provide an important contribution to the otherwise limited knowledge about GNP interference with B cell immune function, and demonstrate that GNPs represent a safe tool to target ABCs in vivo for potential clinical applications. Journal Article ACS Nano 16 11 18119 18132 American Chemical Society (ACS) 1936-0851 1936-086X gold nanoparticles; polymer-coating; in vivo toxicity; targeted delivery, B cells, age-associated B cells 27 10 2022 2022-10-27 10.1021/acsnano.2c04871 PMCID# PMC9706664 COLLEGE NANME Biomedical Sciences COLLEGE CODE BMS Swansea University SU Library paid the OA fee (TA Institutional Deal) Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung - 156372, 156871, 182317; Adolphe Merkle Foundation 2023-09-13T14:51:08.7616929 2022-10-24T10:36:09.7974385 Faculty of Medicine, Health and Life Sciences Swansea University Medical School - Medicine Sandra Hočevar 0000-0002-9770-8229 1 Viola Puddinu 0000-0001-8102-6429 2 Laetitia Haeni 3 Alke Petri-Fink 0000-0003-3952-7849 4 Julia Wagner 5 Montserrat Alvarez 6 Martin Clift 0000-0001-6133-3368 7 Carole Bourquin 0000-0003-3862-4583 8 61638__25754__15d597709481475d81f5dbab4386abdf.pdf 61638.pdf 2022-11-14T10:54:49.9234611 Output 5143439 application/pdf Version of Record true Released under the terms of a Creative Commons Attribution 4.0 International (CC BY 4.0) License. true eng https://creativecommons.org/licenses/by/4.0/
title PEGylated Gold Nanoparticles Target Age-Associated B Cells In Vivo
spellingShingle PEGylated Gold Nanoparticles Target Age-Associated B Cells In Vivo
Martin Clift
title_short PEGylated Gold Nanoparticles Target Age-Associated B Cells In Vivo
title_full PEGylated Gold Nanoparticles Target Age-Associated B Cells In Vivo
title_fullStr PEGylated Gold Nanoparticles Target Age-Associated B Cells In Vivo
title_full_unstemmed PEGylated Gold Nanoparticles Target Age-Associated B Cells In Vivo
title_sort PEGylated Gold Nanoparticles Target Age-Associated B Cells In Vivo
author_id_str_mv 71bf49b157691e541950f5c3f49c9169
author_id_fullname_str_mv 71bf49b157691e541950f5c3f49c9169_***_Martin Clift
author Martin Clift
author2 Sandra Hočevar
Viola Puddinu
Laetitia Haeni
Alke Petri-Fink
Julia Wagner
Montserrat Alvarez
Martin Clift
Carole Bourquin
format Journal article
container_title ACS Nano
container_volume 16
container_issue 11
container_start_page 18119
publishDate 2022
institution Swansea University
issn 1936-0851
1936-086X
doi_str_mv 10.1021/acsnano.2c04871
publisher American Chemical Society (ACS)
college_str Faculty of Medicine, Health and Life Sciences
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hierarchy_top_id facultyofmedicinehealthandlifesciences
hierarchy_top_title Faculty of Medicine, Health and Life Sciences
hierarchy_parent_id facultyofmedicinehealthandlifesciences
hierarchy_parent_title Faculty of Medicine, Health and Life Sciences
department_str Swansea University Medical School - Medicine{{{_:::_}}}Faculty of Medicine, Health and Life Sciences{{{_:::_}}}Swansea University Medical School - Medicine
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description Engineered gold nanoparticles (GNPs) have become a useful tool in various therapeutic and diagnostic applications. Uncertainty remains regarding the possible impact of GNPs on the immune system. In this regard, we investigated the interactions of polymer-coated GNPs with B cells and their functions in mice. Surprisingly, we observed that polymer-coated GNPs mainly interact with the recently identified subpopulation of B lymphocytes named age-associated B cells (ABCs). Importantly, we also showed that GNPs did not affect cell viability or the percentages of other B cell populations in different organs. Furthermore, GNPs did not activate B cell innate-like immune responses in any of the tested conditions, nor did they impair adaptive B cell responses in immunized mice. Together, these data provide an important contribution to the otherwise limited knowledge about GNP interference with B cell immune function, and demonstrate that GNPs represent a safe tool to target ABCs in vivo for potential clinical applications.
published_date 2022-10-27T14:51:10Z
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