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A novel platform for attenuating immune hyperactivity using EXO‐CD24 in COVID‐19 and beyond

A small but significant proportion of COVID‐19 patients develop life‐threatening cytokine storm. We have developed a new anti‐inflammatory drug, EXO‐CD24, a combination of an immune checkpoint (CD24) and a delivery platform (exosomes). CD24 inhibits the NF‐kB pathway and the production of cytokines/...

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Detalles Bibliográficos
Autores principales: Shapira, Shiran, Ben Shimon, Marina, Hay‐Levi, Mori, Shenberg, Gil, Choshen, Guy, Bannon, Lian, Tepper, Michael, Kazanov, Dina, Seni, Jonathan, Lev‐Ari, Shahar, Peer, Michael, Boubas, Dimitrios, Stebbing, Justin, Tsiodras, Sotirios, Arber, Nadir
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9349550/
https://www.ncbi.nlm.nih.gov/pubmed/35776000
http://dx.doi.org/10.15252/emmm.202215997
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author Shapira, Shiran
Ben Shimon, Marina
Hay‐Levi, Mori
Shenberg, Gil
Choshen, Guy
Bannon, Lian
Tepper, Michael
Kazanov, Dina
Seni, Jonathan
Lev‐Ari, Shahar
Peer, Michael
Boubas, Dimitrios
Stebbing, Justin
Tsiodras, Sotirios
Arber, Nadir
author_facet Shapira, Shiran
Ben Shimon, Marina
Hay‐Levi, Mori
Shenberg, Gil
Choshen, Guy
Bannon, Lian
Tepper, Michael
Kazanov, Dina
Seni, Jonathan
Lev‐Ari, Shahar
Peer, Michael
Boubas, Dimitrios
Stebbing, Justin
Tsiodras, Sotirios
Arber, Nadir
author_sort Shapira, Shiran
collection PubMed
description A small but significant proportion of COVID‐19 patients develop life‐threatening cytokine storm. We have developed a new anti‐inflammatory drug, EXO‐CD24, a combination of an immune checkpoint (CD24) and a delivery platform (exosomes). CD24 inhibits the NF‐kB pathway and the production of cytokines/chemokines. EXO‐CD24 discriminates damage‐from pathogen‐associated molecular patterns (DAMPs and PAMPs) therefore does not interfere with viral clearance. EXO‐CD24 was produced and purified from CD24‐expressing 293‐TREx™ cells. Exosomes displaying murine CD24 (mCD24) were also created. EXO‐CD24/mCD24 were characterized and examined, for safety and efficacy, in vitro and in vivo. In a phase Ib/IIa study, 35 patients with moderate–high severity COVID‐19 were recruited and given escalating doses, 10(8)–10(10), of EXO‐CD24 by inhalation, QD, for 5 days. No adverse events related to the drug were observed up to 443–575 days. EXO‐CD24 effectively reduced inflammatory markers and cytokine/chemokine, although randomized studies are required. EXO‐CD24 may be a treatment strategy to suppress the hyper‐inflammatory response in the lungs of COVID‐19 patients and further serve as a therapeutic platform for other pulmonary and systemic diseases characterized by cytokine storm.
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spelling pubmed-93495502022-08-04 A novel platform for attenuating immune hyperactivity using EXO‐CD24 in COVID‐19 and beyond Shapira, Shiran Ben Shimon, Marina Hay‐Levi, Mori Shenberg, Gil Choshen, Guy Bannon, Lian Tepper, Michael Kazanov, Dina Seni, Jonathan Lev‐Ari, Shahar Peer, Michael Boubas, Dimitrios Stebbing, Justin Tsiodras, Sotirios Arber, Nadir EMBO Mol Med Articles A small but significant proportion of COVID‐19 patients develop life‐threatening cytokine storm. We have developed a new anti‐inflammatory drug, EXO‐CD24, a combination of an immune checkpoint (CD24) and a delivery platform (exosomes). CD24 inhibits the NF‐kB pathway and the production of cytokines/chemokines. EXO‐CD24 discriminates damage‐from pathogen‐associated molecular patterns (DAMPs and PAMPs) therefore does not interfere with viral clearance. EXO‐CD24 was produced and purified from CD24‐expressing 293‐TREx™ cells. Exosomes displaying murine CD24 (mCD24) were also created. EXO‐CD24/mCD24 were characterized and examined, for safety and efficacy, in vitro and in vivo. In a phase Ib/IIa study, 35 patients with moderate–high severity COVID‐19 were recruited and given escalating doses, 10(8)–10(10), of EXO‐CD24 by inhalation, QD, for 5 days. No adverse events related to the drug were observed up to 443–575 days. EXO‐CD24 effectively reduced inflammatory markers and cytokine/chemokine, although randomized studies are required. EXO‐CD24 may be a treatment strategy to suppress the hyper‐inflammatory response in the lungs of COVID‐19 patients and further serve as a therapeutic platform for other pulmonary and systemic diseases characterized by cytokine storm. John Wiley and Sons Inc. 2022-07-13 /pmc/articles/PMC9349550/ /pubmed/35776000 http://dx.doi.org/10.15252/emmm.202215997 Text en © 2022 The Authors. Published under the terms of the CC BY 4.0 license. 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 Articles
Shapira, Shiran
Ben Shimon, Marina
Hay‐Levi, Mori
Shenberg, Gil
Choshen, Guy
Bannon, Lian
Tepper, Michael
Kazanov, Dina
Seni, Jonathan
Lev‐Ari, Shahar
Peer, Michael
Boubas, Dimitrios
Stebbing, Justin
Tsiodras, Sotirios
Arber, Nadir
A novel platform for attenuating immune hyperactivity using EXO‐CD24 in COVID‐19 and beyond
title A novel platform for attenuating immune hyperactivity using EXO‐CD24 in COVID‐19 and beyond
title_full A novel platform for attenuating immune hyperactivity using EXO‐CD24 in COVID‐19 and beyond
title_fullStr A novel platform for attenuating immune hyperactivity using EXO‐CD24 in COVID‐19 and beyond
title_full_unstemmed A novel platform for attenuating immune hyperactivity using EXO‐CD24 in COVID‐19 and beyond
title_short A novel platform for attenuating immune hyperactivity using EXO‐CD24 in COVID‐19 and beyond
title_sort novel platform for attenuating immune hyperactivity using exo‐cd24 in covid‐19 and beyond
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9349550/
https://www.ncbi.nlm.nih.gov/pubmed/35776000
http://dx.doi.org/10.15252/emmm.202215997
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