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LAG3-PD-1 Combo Overcome the Disadvantage of Drug Resistance

Although PD-1 blockade therapy has been promising in cancer treatment, only 4% (pancreatic cancer) to 70% (melanoma) of patients have a positive response to this blockade therapy, which is one of its important disadvantages. Therefore, it is important to seek out new targets for cancer immunotherapy...

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Detalles Bibliográficos
Autores principales: Wei, Yiming, Li, Zhaoming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9048820/
https://www.ncbi.nlm.nih.gov/pubmed/35494015
http://dx.doi.org/10.3389/fonc.2022.831407
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author Wei, Yiming
Li, Zhaoming
author_facet Wei, Yiming
Li, Zhaoming
author_sort Wei, Yiming
collection PubMed
description Although PD-1 blockade therapy has been promising in cancer treatment, only 4% (pancreatic cancer) to 70% (melanoma) of patients have a positive response to this blockade therapy, which is one of its important disadvantages. Therefore, it is important to seek out new targets for cancer immunotherapy to improve the overall response rate in patients. Lymphocyte activation gene-3 (LAG-3), an immune checkpoint receptor, is mainly expressed in activated immune cells. LAG-3 maintains the body’s immune homeostasis under physiological conditions while mediating tumour immune escape. Several preclinical and clinical examinations have shown that LAG-3 blockade effectively alleviates the patient’s tolerance to PD-1 immune checkpoint inhibitors. Moreover, the combination of LAG-3 and PD-1 blockade has good clinical efficacy in cancers. Hence, synchronous LAG-3 and PD-1 inhibition may be a potential new strategy for tumour immunotherapy.
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spelling pubmed-90488202022-04-29 LAG3-PD-1 Combo Overcome the Disadvantage of Drug Resistance Wei, Yiming Li, Zhaoming Front Oncol Oncology Although PD-1 blockade therapy has been promising in cancer treatment, only 4% (pancreatic cancer) to 70% (melanoma) of patients have a positive response to this blockade therapy, which is one of its important disadvantages. Therefore, it is important to seek out new targets for cancer immunotherapy to improve the overall response rate in patients. Lymphocyte activation gene-3 (LAG-3), an immune checkpoint receptor, is mainly expressed in activated immune cells. LAG-3 maintains the body’s immune homeostasis under physiological conditions while mediating tumour immune escape. Several preclinical and clinical examinations have shown that LAG-3 blockade effectively alleviates the patient’s tolerance to PD-1 immune checkpoint inhibitors. Moreover, the combination of LAG-3 and PD-1 blockade has good clinical efficacy in cancers. Hence, synchronous LAG-3 and PD-1 inhibition may be a potential new strategy for tumour immunotherapy. Frontiers Media S.A. 2022-04-14 /pmc/articles/PMC9048820/ /pubmed/35494015 http://dx.doi.org/10.3389/fonc.2022.831407 Text en Copyright © 2022 Wei and Li https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Oncology
Wei, Yiming
Li, Zhaoming
LAG3-PD-1 Combo Overcome the Disadvantage of Drug Resistance
title LAG3-PD-1 Combo Overcome the Disadvantage of Drug Resistance
title_full LAG3-PD-1 Combo Overcome the Disadvantage of Drug Resistance
title_fullStr LAG3-PD-1 Combo Overcome the Disadvantage of Drug Resistance
title_full_unstemmed LAG3-PD-1 Combo Overcome the Disadvantage of Drug Resistance
title_short LAG3-PD-1 Combo Overcome the Disadvantage of Drug Resistance
title_sort lag3-pd-1 combo overcome the disadvantage of drug resistance
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9048820/
https://www.ncbi.nlm.nih.gov/pubmed/35494015
http://dx.doi.org/10.3389/fonc.2022.831407
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