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Nanoreporter for Real‐Time Monitoring of Inflammasome Activity and Targeted Therapy

Inflammasome activation is associated with a myriad of inflammatory diseases. However, existing methods provides a limited understanding of spatiotemporal kinetics of inflammasome activation, with restricted scope for early detection of associated treatment efficacy. This limitation offers an opport...

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Detalles Bibliográficos
Autores principales: Nandi, Dipika, Forster, James, Ramesh, Anujan, Nguyen, Anh, Bharadwaj, Hariharan, Kulkarni, Ashish
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9951342/
https://www.ncbi.nlm.nih.gov/pubmed/36603165
http://dx.doi.org/10.1002/advs.202204900
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author Nandi, Dipika
Forster, James
Ramesh, Anujan
Nguyen, Anh
Bharadwaj, Hariharan
Kulkarni, Ashish
author_facet Nandi, Dipika
Forster, James
Ramesh, Anujan
Nguyen, Anh
Bharadwaj, Hariharan
Kulkarni, Ashish
author_sort Nandi, Dipika
collection PubMed
description Inflammasome activation is associated with a myriad of inflammatory diseases. However, existing methods provides a limited understanding of spatiotemporal kinetics of inflammasome activation, with restricted scope for early detection of associated treatment efficacy. This limitation offers an opportunity for the development of biocompatible in‐vivo inflammasome monitoring tools with translational prospects. To achieve this, they report developing a pair of lipid‐based nanoparticle systems, a reporter nanoparticle consisting of a caspase‐1 activatable probe alone, and a theranostic nanoparticle combining the probe with an inflammasome‐inhibiting drug. This biocompatible platform enhances the probe's residence time in circulation by preventing its opsonization and allowing its sustained release over time. Their results demonstrate the specificity of reporter nanoparticles towards caspase‐1 activity and provides early‐on monitoring of inflammasome activation both in‐vitro as well as in‐vivo. Additionally, the delivery of disulfiram, an inflammasome‐inhibiting drug, along with reporter probe using theranostic nanoparticles enables real‐time tracking of treatment efficacy in the gouty‐arthritis inflammatory model. In summary, they report an unparalleled pair of the inflammasome‐associated reporter and theranostic platforms suited not only for diagnostic applications but can also detect inflammasome‐targeted treatment efficiency in real‐time. These findings establish two novel, sensitive nanotools for non‐invasive evaluation of inflammasome‐targeted immunotherapy.
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spelling pubmed-99513422023-02-25 Nanoreporter for Real‐Time Monitoring of Inflammasome Activity and Targeted Therapy Nandi, Dipika Forster, James Ramesh, Anujan Nguyen, Anh Bharadwaj, Hariharan Kulkarni, Ashish Adv Sci (Weinh) Research Articles Inflammasome activation is associated with a myriad of inflammatory diseases. However, existing methods provides a limited understanding of spatiotemporal kinetics of inflammasome activation, with restricted scope for early detection of associated treatment efficacy. This limitation offers an opportunity for the development of biocompatible in‐vivo inflammasome monitoring tools with translational prospects. To achieve this, they report developing a pair of lipid‐based nanoparticle systems, a reporter nanoparticle consisting of a caspase‐1 activatable probe alone, and a theranostic nanoparticle combining the probe with an inflammasome‐inhibiting drug. This biocompatible platform enhances the probe's residence time in circulation by preventing its opsonization and allowing its sustained release over time. Their results demonstrate the specificity of reporter nanoparticles towards caspase‐1 activity and provides early‐on monitoring of inflammasome activation both in‐vitro as well as in‐vivo. Additionally, the delivery of disulfiram, an inflammasome‐inhibiting drug, along with reporter probe using theranostic nanoparticles enables real‐time tracking of treatment efficacy in the gouty‐arthritis inflammatory model. In summary, they report an unparalleled pair of the inflammasome‐associated reporter and theranostic platforms suited not only for diagnostic applications but can also detect inflammasome‐targeted treatment efficiency in real‐time. These findings establish two novel, sensitive nanotools for non‐invasive evaluation of inflammasome‐targeted immunotherapy. John Wiley and Sons Inc. 2023-01-05 /pmc/articles/PMC9951342/ /pubmed/36603165 http://dx.doi.org/10.1002/advs.202204900 Text en © 2023 The Authors. Advanced Science published by Wiley‐VCH GmbH https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Nandi, Dipika
Forster, James
Ramesh, Anujan
Nguyen, Anh
Bharadwaj, Hariharan
Kulkarni, Ashish
Nanoreporter for Real‐Time Monitoring of Inflammasome Activity and Targeted Therapy
title Nanoreporter for Real‐Time Monitoring of Inflammasome Activity and Targeted Therapy
title_full Nanoreporter for Real‐Time Monitoring of Inflammasome Activity and Targeted Therapy
title_fullStr Nanoreporter for Real‐Time Monitoring of Inflammasome Activity and Targeted Therapy
title_full_unstemmed Nanoreporter for Real‐Time Monitoring of Inflammasome Activity and Targeted Therapy
title_short Nanoreporter for Real‐Time Monitoring of Inflammasome Activity and Targeted Therapy
title_sort nanoreporter for real‐time monitoring of inflammasome activity and targeted therapy
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9951342/
https://www.ncbi.nlm.nih.gov/pubmed/36603165
http://dx.doi.org/10.1002/advs.202204900
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