Induction of Innate Memory in Human Monocytes Exposed to Mixtures of Bacterial Agents and Nanoparticles

We assessed whether concomitant exposure of human monocytes to bacterial agents and different engineered nanoparticles can affect the induction of protective innate memory, an immune mechanism that affords better resistance to diverse threatening challenges. Monocytes were exposed in vitro to nanopa...

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Detalhes bibliográficos
Autores: Della Camera, Giacomo, Liu, Tinghao, Yang, Wenjie, Li, Yang|||0000-0001-7242-4687, Puntes, Víctor|||0000-0001-8996-9499, Gioria, Sabrina|||0000-0001-7150-9523, Italiani, Paola|||0000-0001-9830-2733, Boraschi, Diana|||0000-0002-3953-4056
Formato: artículo
Fecha de publicación:2022
País:España
Recursos:Universitat Autònoma de Barcelona
Repositorio:Dipòsit Digital de Documents de la UAB
Idioma:inglés
OAI Identifier:oai:ddd.uab.cat:273649
Acesso em linha:https://ddd.uab.cat/record/273649
https://dx.doi.org/urn:doi:10.3390/ijms232314655
Access Level:acceso abierto
Palavra-chave:Innate immunity
Innate memory
Nanoparticles
Bacteria
LPS
Monocytes
Macrophages
Descrição
Resumo:We assessed whether concomitant exposure of human monocytes to bacterial agents and different engineered nanoparticles can affect the induction of protective innate memory, an immune mechanism that affords better resistance to diverse threatening challenges. Monocytes were exposed in vitro to nanoparticles of different chemical nature, shape and size either alone or admixed with LPS, and cell activation was assessed in terms of production of inflammatory (TNFα, IL-6) and anti-inflammatory cytokines (IL-10, IL-1Ra). After return to baseline conditions, cells were re-challenged with LPS and their secondary "memory" response measured. Results show that nanoparticles alone are essentially unable to generate memory, while LPS induced a tolerance memory response (less inflammatory cytokines, equal or increased anti-inflammatory cytokines). LPS-induced tolerance was not significantly affected by the presence of nanoparticles during the memory generation phase, although with substantial donor-to-donor variability. This suggests that, despite the overall lack of significant effects on LPS-induced innate memory, nanoparticles may have donor-specific effects. Thus, future nanosafety assessment and nanotherapeutic strategies will need a personalized approach in order to ensure both the safety and efficacy of nano medical compounds for individual patients.