Antibodies against the multifaceted cathepsin D protein open new avenues for TNBC immunotherapy

Triple-negative breast cancer (TNBC) is a heterogeneous breast cancer subtype characterized by aggressive clinical behavior and poor prognosis. The immune landscape associated with TNBC often reveals high immunogenicity. Therefore, immunotherapy, which has demonstrated its efficacy in different canc...

Full description

Saved in:
Bibliographic Details
Main Authors: Valérie Laurent-Matha, Pascal Roger, Séverine Guiu, Thierry Chardès, Emmanuelle Liaudet-Coopman, Pénélope Desroys du Roure, Timothée David, Aude Mallavialle
Format: Article
Language:English
Published: BMJ Publishing Group 2025-01-01
Series:Journal for ImmunoTherapy of Cancer
Online Access:https://jitc.bmj.com/content/13/1/e009548.full
Tags: Add Tag
No Tags, Be the first to tag this record!
_version_ 1841536291924082688
author Valérie Laurent-Matha
Pascal Roger
Séverine Guiu
Thierry Chardès
Emmanuelle Liaudet-Coopman
Pénélope Desroys du Roure
Timothée David
Aude Mallavialle
author_facet Valérie Laurent-Matha
Pascal Roger
Séverine Guiu
Thierry Chardès
Emmanuelle Liaudet-Coopman
Pénélope Desroys du Roure
Timothée David
Aude Mallavialle
author_sort Valérie Laurent-Matha
collection DOAJ
description Triple-negative breast cancer (TNBC) is a heterogeneous breast cancer subtype characterized by aggressive clinical behavior and poor prognosis. The immune landscape associated with TNBC often reveals high immunogenicity. Therefore, immunotherapy, which has demonstrated its efficacy in different cancer types, could be a promising strategy for TNBC, given the limited therapeutic options currently available besides conventional chemotherapy. The aspartic protease cathepsin D (cath-D) is a tumor cell-associated extracellular protein with protumor activity, a marker of poor prognosis, and a target for antibody-based therapy in TNBC. This commentary provides a synopsis/narrative summary of the development of anti-cath-D antibodies in different formats, their key roles in restoring the antitumor immunity, particularly via activation of tumor-infiltrating natural killer cells, and their dual antitumor effects on cancer cells and stromal cancer-associated fibroblasts, suggesting their interest for clinical use in the light of the current clinical knowledge on TNBC.
format Article
id doaj-art-df7edb8a44c84e268fe124ad32df642a
institution Kabale University
issn 2051-1426
language English
publishDate 2025-01-01
publisher BMJ Publishing Group
record_format Article
series Journal for ImmunoTherapy of Cancer
spelling doaj-art-df7edb8a44c84e268fe124ad32df642a2025-01-14T23:10:11ZengBMJ Publishing GroupJournal for ImmunoTherapy of Cancer2051-14262025-01-0113110.1136/jitc-2024-009548Antibodies against the multifaceted cathepsin D protein open new avenues for TNBC immunotherapyValérie Laurent-Matha0Pascal Roger1Séverine Guiu2Thierry Chardès3Emmanuelle Liaudet-Coopman4Pénélope Desroys du Roure5Timothée David6Aude Mallavialle7IRCM, INSERM U1194, University of Montpellier, ICM, Montpellier, FranceAff1 grid.411439.a0000 0001 2150 9058IRCM, INSERM, U1194 Univ Montpellier, ICM 208, rue des Apothicaires F-34298 Montpellier, Cedex 5 FranceAff1 grid.411439.a0000 0001 2150 9058IRCM, INSERM, U1194 Univ Montpellier, ICM 208, rue des Apothicaires F-34298 Montpellier, Cedex 5 FranceAff1 grid.411439.a0000 0001 2150 9058IRCM, INSERM, U1194 Univ Montpellier, ICM 208, rue des Apothicaires F-34298 Montpellier, Cedex 5 FranceAff1 grid.411439.a0000 0001 2150 9058IRCM, INSERM, U1194 Univ Montpellier, ICM 208, rue des Apothicaires F-34298 Montpellier, Cedex 5 FranceIRCM, INSERM U1194, University of Montpellier, ICM, Montpellier, FranceIRCM, INSERM U1194, University of Montpellier, ICM, Montpellier, FranceIRCM, INSERM U1194, University of Montpellier, ICM, Montpellier, FranceTriple-negative breast cancer (TNBC) is a heterogeneous breast cancer subtype characterized by aggressive clinical behavior and poor prognosis. The immune landscape associated with TNBC often reveals high immunogenicity. Therefore, immunotherapy, which has demonstrated its efficacy in different cancer types, could be a promising strategy for TNBC, given the limited therapeutic options currently available besides conventional chemotherapy. The aspartic protease cathepsin D (cath-D) is a tumor cell-associated extracellular protein with protumor activity, a marker of poor prognosis, and a target for antibody-based therapy in TNBC. This commentary provides a synopsis/narrative summary of the development of anti-cath-D antibodies in different formats, their key roles in restoring the antitumor immunity, particularly via activation of tumor-infiltrating natural killer cells, and their dual antitumor effects on cancer cells and stromal cancer-associated fibroblasts, suggesting their interest for clinical use in the light of the current clinical knowledge on TNBC.https://jitc.bmj.com/content/13/1/e009548.full
spellingShingle Valérie Laurent-Matha
Pascal Roger
Séverine Guiu
Thierry Chardès
Emmanuelle Liaudet-Coopman
Pénélope Desroys du Roure
Timothée David
Aude Mallavialle
Antibodies against the multifaceted cathepsin D protein open new avenues for TNBC immunotherapy
Journal for ImmunoTherapy of Cancer
title Antibodies against the multifaceted cathepsin D protein open new avenues for TNBC immunotherapy
title_full Antibodies against the multifaceted cathepsin D protein open new avenues for TNBC immunotherapy
title_fullStr Antibodies against the multifaceted cathepsin D protein open new avenues for TNBC immunotherapy
title_full_unstemmed Antibodies against the multifaceted cathepsin D protein open new avenues for TNBC immunotherapy
title_short Antibodies against the multifaceted cathepsin D protein open new avenues for TNBC immunotherapy
title_sort antibodies against the multifaceted cathepsin d protein open new avenues for tnbc immunotherapy
url https://jitc.bmj.com/content/13/1/e009548.full
work_keys_str_mv AT valerielaurentmatha antibodiesagainstthemultifacetedcathepsindproteinopennewavenuesfortnbcimmunotherapy
AT pascalroger antibodiesagainstthemultifacetedcathepsindproteinopennewavenuesfortnbcimmunotherapy
AT severineguiu antibodiesagainstthemultifacetedcathepsindproteinopennewavenuesfortnbcimmunotherapy
AT thierrychardes antibodiesagainstthemultifacetedcathepsindproteinopennewavenuesfortnbcimmunotherapy
AT emmanuelleliaudetcoopman antibodiesagainstthemultifacetedcathepsindproteinopennewavenuesfortnbcimmunotherapy
AT penelopedesroysduroure antibodiesagainstthemultifacetedcathepsindproteinopennewavenuesfortnbcimmunotherapy
AT timotheedavid antibodiesagainstthemultifacetedcathepsindproteinopennewavenuesfortnbcimmunotherapy
AT audemallavialle antibodiesagainstthemultifacetedcathepsindproteinopennewavenuesfortnbcimmunotherapy