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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...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society of Hematology
2021
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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. |
format | Online Article Text |
id | pubmed-8945623 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | American Society of Hematology |
record_format | MEDLINE/PubMed |
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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