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IL12 immune therapy clinical trial review: Novel strategies for avoiding CRS-associated cytokines
Interleukin 12 (IL-12) is a naturally occurring cytokine that plays a key role in inducing antitumor immune responses, including induction of antitumor immune memory. Currently, no IL-12-based therapeutic products have been approved for clinical application because of its toxicities. On the basis of...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9530253/ https://www.ncbi.nlm.nih.gov/pubmed/36203573 http://dx.doi.org/10.3389/fimmu.2022.952231 |
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author | Jia, Zhiliang Ragoonanan, Dristhi Mahadeo, Kris Michael Gill, Jonathan Gorlick, Richard Shpal, Elizabeth Li, Shulin |
author_facet | Jia, Zhiliang Ragoonanan, Dristhi Mahadeo, Kris Michael Gill, Jonathan Gorlick, Richard Shpal, Elizabeth Li, Shulin |
author_sort | Jia, Zhiliang |
collection | PubMed |
description | Interleukin 12 (IL-12) is a naturally occurring cytokine that plays a key role in inducing antitumor immune responses, including induction of antitumor immune memory. Currently, no IL-12-based therapeutic products have been approved for clinical application because of its toxicities. On the basis of this review of clinical trials using primarily wild-type IL-12 and different delivery methods, we conclude that the safe utilization of IL-12 is highly dependent on the tumor-specific localization of IL-12 post administration. In this regard, we have developed a cell membrane-anchored and tumor-targeted IL-12-T (attIL12-T) cell product for avoiding toxicity from both IL-12 and T cells-induced cytokine release syndrome in peripheral tissues. A phase I trial using this product which seeks to avoid systemic toxicity and boost antitumor efficacy is on the horizon. Of note, this product also boosts the impact of CAR-T or TCR-T cell efficacy against solid tumors, providing an alternative approach to utilize CAR-T to overcome tumor resistance. |
format | Online Article Text |
id | pubmed-9530253 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-95302532022-10-05 IL12 immune therapy clinical trial review: Novel strategies for avoiding CRS-associated cytokines Jia, Zhiliang Ragoonanan, Dristhi Mahadeo, Kris Michael Gill, Jonathan Gorlick, Richard Shpal, Elizabeth Li, Shulin Front Immunol Immunology Interleukin 12 (IL-12) is a naturally occurring cytokine that plays a key role in inducing antitumor immune responses, including induction of antitumor immune memory. Currently, no IL-12-based therapeutic products have been approved for clinical application because of its toxicities. On the basis of this review of clinical trials using primarily wild-type IL-12 and different delivery methods, we conclude that the safe utilization of IL-12 is highly dependent on the tumor-specific localization of IL-12 post administration. In this regard, we have developed a cell membrane-anchored and tumor-targeted IL-12-T (attIL12-T) cell product for avoiding toxicity from both IL-12 and T cells-induced cytokine release syndrome in peripheral tissues. A phase I trial using this product which seeks to avoid systemic toxicity and boost antitumor efficacy is on the horizon. Of note, this product also boosts the impact of CAR-T or TCR-T cell efficacy against solid tumors, providing an alternative approach to utilize CAR-T to overcome tumor resistance. Frontiers Media S.A. 2022-09-20 /pmc/articles/PMC9530253/ /pubmed/36203573 http://dx.doi.org/10.3389/fimmu.2022.952231 Text en Copyright © 2022 Jia, Ragoonanan, Mahadeo, Gill, Gorlick, Shpal and Li https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Immunology Jia, Zhiliang Ragoonanan, Dristhi Mahadeo, Kris Michael Gill, Jonathan Gorlick, Richard Shpal, Elizabeth Li, Shulin IL12 immune therapy clinical trial review: Novel strategies for avoiding CRS-associated cytokines |
title | IL12 immune therapy clinical trial review: Novel strategies for avoiding CRS-associated cytokines |
title_full | IL12 immune therapy clinical trial review: Novel strategies for avoiding CRS-associated cytokines |
title_fullStr | IL12 immune therapy clinical trial review: Novel strategies for avoiding CRS-associated cytokines |
title_full_unstemmed | IL12 immune therapy clinical trial review: Novel strategies for avoiding CRS-associated cytokines |
title_short | IL12 immune therapy clinical trial review: Novel strategies for avoiding CRS-associated cytokines |
title_sort | il12 immune therapy clinical trial review: novel strategies for avoiding crs-associated cytokines |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9530253/ https://www.ncbi.nlm.nih.gov/pubmed/36203573 http://dx.doi.org/10.3389/fimmu.2022.952231 |
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