Emerging roles of checkpoint molecules on B cells

Immune checkpoint molecules, including both co-inhibitory molecules and co-stimulatory molecules, are known to play critical roles in regulating T-cell responses. During the last decades, immunotherapies targeting these molecules (such as programmed cell death 1 (PD-1), and lymphocyte activation gen...

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Main Authors: Hiromitsu Asashima, Satoshi Akao, Isao Matsumoto
Format: Article
Language:English
Published: Taylor & Francis Group 2025-01-01
Series:Immunological Medicine
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Online Access:https://www.tandfonline.com/doi/10.1080/25785826.2025.2454045
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author Hiromitsu Asashima
Satoshi Akao
Isao Matsumoto
author_facet Hiromitsu Asashima
Satoshi Akao
Isao Matsumoto
author_sort Hiromitsu Asashima
collection DOAJ
description Immune checkpoint molecules, including both co-inhibitory molecules and co-stimulatory molecules, are known to play critical roles in regulating T-cell responses. During the last decades, immunotherapies targeting these molecules (such as programmed cell death 1 (PD-1), and lymphocyte activation gene 3 (LAG-3)) have provided clinical benefits in many cancers. It is becoming apparent that not only T cells, but also B cells have a capacity to express some checkpoint molecules. These were originally thought to be only the markers for regulatory B cells which produce IL-10, but recent studies suggest that these molecules (especially T-cell immunoglobulin and mucin domain 1 (TIM-1), T cell immunoreceptor with Ig and ITIM domains (TIGIT), and PD-1) can regulate intrinsic B-cell activation and functions. Here, we focus on these molecules and summarize their characteristics, ligands, and functions on B cells.
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spelling doaj-art-668f49fc98114cc793c56f353ca9abd82025-01-17T13:26:24ZengTaylor & Francis GroupImmunological Medicine2578-58262025-01-0111210.1080/25785826.2025.2454045Emerging roles of checkpoint molecules on B cellsHiromitsu Asashima0Satoshi Akao1Isao Matsumoto2Department of Rheumatology, Institute of Medicine, University of Tsukuba, Ibaraki, JapanDepartment of Rheumatology, Institute of Medicine, University of Tsukuba, Ibaraki, JapanDepartment of Rheumatology, Institute of Medicine, University of Tsukuba, Ibaraki, JapanImmune checkpoint molecules, including both co-inhibitory molecules and co-stimulatory molecules, are known to play critical roles in regulating T-cell responses. During the last decades, immunotherapies targeting these molecules (such as programmed cell death 1 (PD-1), and lymphocyte activation gene 3 (LAG-3)) have provided clinical benefits in many cancers. It is becoming apparent that not only T cells, but also B cells have a capacity to express some checkpoint molecules. These were originally thought to be only the markers for regulatory B cells which produce IL-10, but recent studies suggest that these molecules (especially T-cell immunoglobulin and mucin domain 1 (TIM-1), T cell immunoreceptor with Ig and ITIM domains (TIGIT), and PD-1) can regulate intrinsic B-cell activation and functions. Here, we focus on these molecules and summarize their characteristics, ligands, and functions on B cells.https://www.tandfonline.com/doi/10.1080/25785826.2025.2454045Regulatory B cellscheckpoint moleculesTIM-1TIGITPD-1
spellingShingle Hiromitsu Asashima
Satoshi Akao
Isao Matsumoto
Emerging roles of checkpoint molecules on B cells
Immunological Medicine
Regulatory B cells
checkpoint molecules
TIM-1
TIGIT
PD-1
title Emerging roles of checkpoint molecules on B cells
title_full Emerging roles of checkpoint molecules on B cells
title_fullStr Emerging roles of checkpoint molecules on B cells
title_full_unstemmed Emerging roles of checkpoint molecules on B cells
title_short Emerging roles of checkpoint molecules on B cells
title_sort emerging roles of checkpoint molecules on b cells
topic Regulatory B cells
checkpoint molecules
TIM-1
TIGIT
PD-1
url https://www.tandfonline.com/doi/10.1080/25785826.2025.2454045
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AT satoshiakao emergingrolesofcheckpointmoleculesonbcells
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