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Derivation and Preclinical Characterization of CYT-303, a Novel NKp46-NK Cell Engager Targeting GPC3

Glypican-3 (GPC3) is an oncofetal antigen that is highly expressed in multiple solid tumors, including hepatocellular carcinoma, and is barely expressed in adult normal tissues except the placenta. NKp46 activation receptor is expressed in all-natural killer (NK) cells, including tumor-infiltrating...

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Autores principales: Arulanandam, Antonio, Lin, Liang, Chang, Hao-Ming, Cerutti, Martine, Choblet, Sylvie, Gao, Peng, Rath, Armin, Bensussan, Armand, Kadouche, Jean, Teper, Daniel, Mandelboim, Ofer, Li, Wei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10093649/
https://www.ncbi.nlm.nih.gov/pubmed/37048069
http://dx.doi.org/10.3390/cells12070996
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author Arulanandam, Antonio
Lin, Liang
Chang, Hao-Ming
Cerutti, Martine
Choblet, Sylvie
Gao, Peng
Rath, Armin
Bensussan, Armand
Kadouche, Jean
Teper, Daniel
Mandelboim, Ofer
Li, Wei
author_facet Arulanandam, Antonio
Lin, Liang
Chang, Hao-Ming
Cerutti, Martine
Choblet, Sylvie
Gao, Peng
Rath, Armin
Bensussan, Armand
Kadouche, Jean
Teper, Daniel
Mandelboim, Ofer
Li, Wei
author_sort Arulanandam, Antonio
collection PubMed
description Glypican-3 (GPC3) is an oncofetal antigen that is highly expressed in multiple solid tumors, including hepatocellular carcinoma, and is barely expressed in adult normal tissues except the placenta. NKp46 activation receptor is expressed in all-natural killer (NK) cells, including tumor-infiltrating NK cells. FLEX-NK(TM) is a platform for the production of tetravalent multifunctional antibody NK cell engagers (NKE). CYT-303 was designed using the FLEX-NK scaffold, incorporating a novel humanized NKp46 binder that does not induce NKp46 internalization and a humanized GPC3 binder that targets the membrane-proximal lobe to mediate NK cell-redirected killing of HCC tumors. CYT-303 shows sub-nanomolar binding affinities to both GPC3 and NKp46. CYT-303 was highly potent and effective in mediating NK cell-redirected cytotoxicity against multiple HCC tumor cell lines and tumor spheroids. More interestingly, it can reverse the dysfunction induced in NK cells following repeated rounds of serial killing of tumors. It also mediated antibody-dependent cellular phagocytosis (ADCP) and complement-dependent cytotoxicity against GPC3-expressing HCC tumors. In vivo, CYT-303 showed no toxicity or cytokine release in cynomolgus monkeys up to the highest dose (60 mg/kg), administered weekly by intravenous infusion for 28 days. These results demonstrate the potential of CYT-303 to be a safe and effective therapy against HCC.
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spelling pubmed-100936492023-04-13 Derivation and Preclinical Characterization of CYT-303, a Novel NKp46-NK Cell Engager Targeting GPC3 Arulanandam, Antonio Lin, Liang Chang, Hao-Ming Cerutti, Martine Choblet, Sylvie Gao, Peng Rath, Armin Bensussan, Armand Kadouche, Jean Teper, Daniel Mandelboim, Ofer Li, Wei Cells Article Glypican-3 (GPC3) is an oncofetal antigen that is highly expressed in multiple solid tumors, including hepatocellular carcinoma, and is barely expressed in adult normal tissues except the placenta. NKp46 activation receptor is expressed in all-natural killer (NK) cells, including tumor-infiltrating NK cells. FLEX-NK(TM) is a platform for the production of tetravalent multifunctional antibody NK cell engagers (NKE). CYT-303 was designed using the FLEX-NK scaffold, incorporating a novel humanized NKp46 binder that does not induce NKp46 internalization and a humanized GPC3 binder that targets the membrane-proximal lobe to mediate NK cell-redirected killing of HCC tumors. CYT-303 shows sub-nanomolar binding affinities to both GPC3 and NKp46. CYT-303 was highly potent and effective in mediating NK cell-redirected cytotoxicity against multiple HCC tumor cell lines and tumor spheroids. More interestingly, it can reverse the dysfunction induced in NK cells following repeated rounds of serial killing of tumors. It also mediated antibody-dependent cellular phagocytosis (ADCP) and complement-dependent cytotoxicity against GPC3-expressing HCC tumors. In vivo, CYT-303 showed no toxicity or cytokine release in cynomolgus monkeys up to the highest dose (60 mg/kg), administered weekly by intravenous infusion for 28 days. These results demonstrate the potential of CYT-303 to be a safe and effective therapy against HCC. MDPI 2023-03-24 /pmc/articles/PMC10093649/ /pubmed/37048069 http://dx.doi.org/10.3390/cells12070996 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Arulanandam, Antonio
Lin, Liang
Chang, Hao-Ming
Cerutti, Martine
Choblet, Sylvie
Gao, Peng
Rath, Armin
Bensussan, Armand
Kadouche, Jean
Teper, Daniel
Mandelboim, Ofer
Li, Wei
Derivation and Preclinical Characterization of CYT-303, a Novel NKp46-NK Cell Engager Targeting GPC3
title Derivation and Preclinical Characterization of CYT-303, a Novel NKp46-NK Cell Engager Targeting GPC3
title_full Derivation and Preclinical Characterization of CYT-303, a Novel NKp46-NK Cell Engager Targeting GPC3
title_fullStr Derivation and Preclinical Characterization of CYT-303, a Novel NKp46-NK Cell Engager Targeting GPC3
title_full_unstemmed Derivation and Preclinical Characterization of CYT-303, a Novel NKp46-NK Cell Engager Targeting GPC3
title_short Derivation and Preclinical Characterization of CYT-303, a Novel NKp46-NK Cell Engager Targeting GPC3
title_sort derivation and preclinical characterization of cyt-303, a novel nkp46-nk cell engager targeting gpc3
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10093649/
https://www.ncbi.nlm.nih.gov/pubmed/37048069
http://dx.doi.org/10.3390/cells12070996
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