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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/...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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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. |
format | Online Article Text |
id | pubmed-9349550 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
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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