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Lymphocyte‐activation gene‐3, an important immune checkpoint in cancer

Immunotherapy has recently become widely used in lung cancer. Many oncologists are focused on cytotoxic T lymphocyte antigen‐4 (CTLA‐4), programmed cell death ligand‐1 (PD‐L1) and programmed cell death‐1 (PD‐1). Immunotherapy targeting the PD‐1/PD‐L1 checkpoints has shown promising efficacy in non‐s...

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Autores principales: He, Yayi, Rivard, Christopher J., Rozeboom, Leslie, Yu, Hui, Ellison, Kim, Kowalewski, Ashley, Zhou, Caicun, Hirsch, Fred R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5021038/
https://www.ncbi.nlm.nih.gov/pubmed/27297395
http://dx.doi.org/10.1111/cas.12986
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author He, Yayi
Rivard, Christopher J.
Rozeboom, Leslie
Yu, Hui
Ellison, Kim
Kowalewski, Ashley
Zhou, Caicun
Hirsch, Fred R.
author_facet He, Yayi
Rivard, Christopher J.
Rozeboom, Leslie
Yu, Hui
Ellison, Kim
Kowalewski, Ashley
Zhou, Caicun
Hirsch, Fred R.
author_sort He, Yayi
collection PubMed
description Immunotherapy has recently become widely used in lung cancer. Many oncologists are focused on cytotoxic T lymphocyte antigen‐4 (CTLA‐4), programmed cell death ligand‐1 (PD‐L1) and programmed cell death‐1 (PD‐1). Immunotherapy targeting the PD‐1/PD‐L1 checkpoints has shown promising efficacy in non‐small cell lung cancer (NSCLC), but questions remain to be answered. Among them is whether the simultaneous inhibition of other checkpoints could improve outcomes. Lymphocyte‐activation gene‐3 (LAG‐3) is another vital checkpoint that may have a synergistic interaction with PD‐1/PD‐L1. Here we review the LAG‐3 function in cancer, clinical trials with agents targeting LAG‐3 and the correlation of LAG‐3 with other checkpoints.
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spelling pubmed-50210382016-09-20 Lymphocyte‐activation gene‐3, an important immune checkpoint in cancer He, Yayi Rivard, Christopher J. Rozeboom, Leslie Yu, Hui Ellison, Kim Kowalewski, Ashley Zhou, Caicun Hirsch, Fred R. Cancer Sci Review Articles Immunotherapy has recently become widely used in lung cancer. Many oncologists are focused on cytotoxic T lymphocyte antigen‐4 (CTLA‐4), programmed cell death ligand‐1 (PD‐L1) and programmed cell death‐1 (PD‐1). Immunotherapy targeting the PD‐1/PD‐L1 checkpoints has shown promising efficacy in non‐small cell lung cancer (NSCLC), but questions remain to be answered. Among them is whether the simultaneous inhibition of other checkpoints could improve outcomes. Lymphocyte‐activation gene‐3 (LAG‐3) is another vital checkpoint that may have a synergistic interaction with PD‐1/PD‐L1. Here we review the LAG‐3 function in cancer, clinical trials with agents targeting LAG‐3 and the correlation of LAG‐3 with other checkpoints. John Wiley and Sons Inc. 2016-08-25 2016-09 /pmc/articles/PMC5021038/ /pubmed/27297395 http://dx.doi.org/10.1111/cas.12986 Text en © 2016 The Authors. Cancer Science published by John Wiley & Sons Australia, Ltd on behalf of Japanese Cancer Association. This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial‐NoDerivs (http://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Review Articles
He, Yayi
Rivard, Christopher J.
Rozeboom, Leslie
Yu, Hui
Ellison, Kim
Kowalewski, Ashley
Zhou, Caicun
Hirsch, Fred R.
Lymphocyte‐activation gene‐3, an important immune checkpoint in cancer
title Lymphocyte‐activation gene‐3, an important immune checkpoint in cancer
title_full Lymphocyte‐activation gene‐3, an important immune checkpoint in cancer
title_fullStr Lymphocyte‐activation gene‐3, an important immune checkpoint in cancer
title_full_unstemmed Lymphocyte‐activation gene‐3, an important immune checkpoint in cancer
title_short Lymphocyte‐activation gene‐3, an important immune checkpoint in cancer
title_sort lymphocyte‐activation gene‐3, an important immune checkpoint in cancer
topic Review Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5021038/
https://www.ncbi.nlm.nih.gov/pubmed/27297395
http://dx.doi.org/10.1111/cas.12986
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