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Antagonism of inhibitors of apoptosis proteins reveals a novel, immune response-based therapeutic approach for T-cell lymphoma

Tolinapant (ASTX660) is a potent, nonpeptidomimetic antagonist of cellular inhibitor of apoptosis proteins 1 and 2 (cIAP1/2) and X-linked IAP, which is currently being evaluated in a phase 2 study in T-cell lymphoma (TCL) patients. Tolinapant has demonstrated evidence of single-agent clinical activi...

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Autores principales: Ferrari, Nicola, Ward, George, Gewinner, Christina, Davis, Matthew P., Jueliger, Simone, Saini, Harpreet, Munck, Joanne, Smyth, Tomoko, Ferraldeschi, Roberta, Keer, Harold, Lyons, John, Sims, Martin J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society of Hematology 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8945623/
https://www.ncbi.nlm.nih.gov/pubmed/34474469
http://dx.doi.org/10.1182/bloodadvances.2020003955
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author Ferrari, Nicola
Ward, George
Gewinner, Christina
Davis, Matthew P.
Jueliger, Simone
Saini, Harpreet
Munck, Joanne
Smyth, Tomoko
Ferraldeschi, Roberta
Keer, Harold
Lyons, John
Sims, Martin J.
author_facet Ferrari, Nicola
Ward, George
Gewinner, Christina
Davis, Matthew P.
Jueliger, Simone
Saini, Harpreet
Munck, Joanne
Smyth, Tomoko
Ferraldeschi, Roberta
Keer, Harold
Lyons, John
Sims, Martin J.
author_sort Ferrari, Nicola
collection PubMed
description Tolinapant (ASTX660) is a potent, nonpeptidomimetic antagonist of cellular inhibitor of apoptosis proteins 1 and 2 (cIAP1/2) and X-linked IAP, which is currently being evaluated in a phase 2 study in T-cell lymphoma (TCL) patients. Tolinapant has demonstrated evidence of single-agent clinical activity in relapsed/refractory peripheral TCL and cutaneous TCL. To investigate the mechanism of action underlying the single-agent activity observed in the clinic, we have used a comprehensive translational approach integrating in vitro and in vivo models of TCL confirmed by data from human tumor biopsies. Here, we show that tolinapant acts as an efficacious immunomodulatory molecule capable of inducing complete tumor regression in a syngeneic model of TCL exclusively in the presence of an intact immune system. These findings were confirmed in samples from our ongoing clinical study showing that tolinapant treatment can induce changes in gene expression and cytokine profile consistent with immune modulation. Mechanistically, we show that tolinapant can activate both the adaptive and the innate arms of the immune system through the induction of immunogenic forms of cell death. In summary, we describe a novel role for IAP antagonists as immunomodulatory molecules capable of promoting a robust antitumor immune response in TCL.
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spelling pubmed-89456232022-03-29 Antagonism of inhibitors of apoptosis proteins reveals a novel, immune response-based therapeutic approach for T-cell lymphoma Ferrari, Nicola Ward, George Gewinner, Christina Davis, Matthew P. Jueliger, Simone Saini, Harpreet Munck, Joanne Smyth, Tomoko Ferraldeschi, Roberta Keer, Harold Lyons, John Sims, Martin J. Blood Adv Immunobiology and Immunotherapy Tolinapant (ASTX660) is a potent, nonpeptidomimetic antagonist of cellular inhibitor of apoptosis proteins 1 and 2 (cIAP1/2) and X-linked IAP, which is currently being evaluated in a phase 2 study in T-cell lymphoma (TCL) patients. Tolinapant has demonstrated evidence of single-agent clinical activity in relapsed/refractory peripheral TCL and cutaneous TCL. To investigate the mechanism of action underlying the single-agent activity observed in the clinic, we have used a comprehensive translational approach integrating in vitro and in vivo models of TCL confirmed by data from human tumor biopsies. Here, we show that tolinapant acts as an efficacious immunomodulatory molecule capable of inducing complete tumor regression in a syngeneic model of TCL exclusively in the presence of an intact immune system. These findings were confirmed in samples from our ongoing clinical study showing that tolinapant treatment can induce changes in gene expression and cytokine profile consistent with immune modulation. Mechanistically, we show that tolinapant can activate both the adaptive and the innate arms of the immune system through the induction of immunogenic forms of cell death. In summary, we describe a novel role for IAP antagonists as immunomodulatory molecules capable of promoting a robust antitumor immune response in TCL. American Society of Hematology 2021-10-19 /pmc/articles/PMC8945623/ /pubmed/34474469 http://dx.doi.org/10.1182/bloodadvances.2020003955 Text en © 2021 by The American Society of Hematology. Licensed under Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0), permitting only noncommercial, nonderivative use with attribution. All other rights reserved.
spellingShingle Immunobiology and Immunotherapy
Ferrari, Nicola
Ward, George
Gewinner, Christina
Davis, Matthew P.
Jueliger, Simone
Saini, Harpreet
Munck, Joanne
Smyth, Tomoko
Ferraldeschi, Roberta
Keer, Harold
Lyons, John
Sims, Martin J.
Antagonism of inhibitors of apoptosis proteins reveals a novel, immune response-based therapeutic approach for T-cell lymphoma
title Antagonism of inhibitors of apoptosis proteins reveals a novel, immune response-based therapeutic approach for T-cell lymphoma
title_full Antagonism of inhibitors of apoptosis proteins reveals a novel, immune response-based therapeutic approach for T-cell lymphoma
title_fullStr Antagonism of inhibitors of apoptosis proteins reveals a novel, immune response-based therapeutic approach for T-cell lymphoma
title_full_unstemmed Antagonism of inhibitors of apoptosis proteins reveals a novel, immune response-based therapeutic approach for T-cell lymphoma
title_short Antagonism of inhibitors of apoptosis proteins reveals a novel, immune response-based therapeutic approach for T-cell lymphoma
title_sort antagonism of inhibitors of apoptosis proteins reveals a novel, immune response-based therapeutic approach for t-cell lymphoma
topic Immunobiology and Immunotherapy
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8945623/
https://www.ncbi.nlm.nih.gov/pubmed/34474469
http://dx.doi.org/10.1182/bloodadvances.2020003955
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