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TIM-3: a tumor-associated antigen beyond checkpoint inhibition?

Immune checkpoint inhibitors are one of the most remarkable immunomodulatory therapies of current times. Sabatolimab is a high-affinity, humanized anti-TIM-3 monoclonal antibody currently in development for patients with myeloproliferative disorders, including acute myeloid leukemia and myelodysplas...

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Detalles Bibliográficos
Autores principales: Barth, Stefan, Naran, Krupa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9669666/
https://www.ncbi.nlm.nih.gov/pubmed/36406467
http://dx.doi.org/10.1093/immadv/ltac021
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author Barth, Stefan
Naran, Krupa
author_facet Barth, Stefan
Naran, Krupa
author_sort Barth, Stefan
collection PubMed
description Immune checkpoint inhibitors are one of the most remarkable immunomodulatory therapies of current times. Sabatolimab is a high-affinity, humanized anti-TIM-3 monoclonal antibody currently in development for patients with myeloproliferative disorders, including acute myeloid leukemia and myelodysplastic syndromes. By targeting TIM-3, a receptor expressed on various immune effector cells as well as myeloid cells, multiple mechanisms of action that are distinct from canonical immune checkpoint inhibitors are in play – (i) blockade of TIM-3 and its ligands PtdSer/galectin-9, (ii) modulation of leukemic cell self-renewal as well as (iii) antibody-dependent phagocytosis of TIM-3–expressing leukemic cells. Novel immunotherapies such as sabatolimab which enhance the antitumor immune response on converging fronts represent the promise of a continuously replenished armoury for the treatment of cancer.
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spelling pubmed-96696662022-11-17 TIM-3: a tumor-associated antigen beyond checkpoint inhibition? Barth, Stefan Naran, Krupa Immunother Adv Commentary Immune checkpoint inhibitors are one of the most remarkable immunomodulatory therapies of current times. Sabatolimab is a high-affinity, humanized anti-TIM-3 monoclonal antibody currently in development for patients with myeloproliferative disorders, including acute myeloid leukemia and myelodysplastic syndromes. By targeting TIM-3, a receptor expressed on various immune effector cells as well as myeloid cells, multiple mechanisms of action that are distinct from canonical immune checkpoint inhibitors are in play – (i) blockade of TIM-3 and its ligands PtdSer/galectin-9, (ii) modulation of leukemic cell self-renewal as well as (iii) antibody-dependent phagocytosis of TIM-3–expressing leukemic cells. Novel immunotherapies such as sabatolimab which enhance the antitumor immune response on converging fronts represent the promise of a continuously replenished armoury for the treatment of cancer. Oxford University Press 2022-10-21 /pmc/articles/PMC9669666/ /pubmed/36406467 http://dx.doi.org/10.1093/immadv/ltac021 Text en © The Author(s) 2022. Published by Oxford University Press on behalf of the British Society for Immunology. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (https://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Commentary
Barth, Stefan
Naran, Krupa
TIM-3: a tumor-associated antigen beyond checkpoint inhibition?
title TIM-3: a tumor-associated antigen beyond checkpoint inhibition?
title_full TIM-3: a tumor-associated antigen beyond checkpoint inhibition?
title_fullStr TIM-3: a tumor-associated antigen beyond checkpoint inhibition?
title_full_unstemmed TIM-3: a tumor-associated antigen beyond checkpoint inhibition?
title_short TIM-3: a tumor-associated antigen beyond checkpoint inhibition?
title_sort tim-3: a tumor-associated antigen beyond checkpoint inhibition?
topic Commentary
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9669666/
https://www.ncbi.nlm.nih.gov/pubmed/36406467
http://dx.doi.org/10.1093/immadv/ltac021
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