ID | 113688 |
Title Alternative | 抑制性免疫補助受容体LAG-3は細胞質領域に有する非定型モチーフを介してT細胞の活性化を抑制する
Inhibitory mechanisms of LAG-3–dependent T cell suppression
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Author |
Maeda, Takeo K.
Tokushima University
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Keywords | T細胞抗原受容体
免疫補助受容体
抑制機構
モノクローナル抗体
LAG-3
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Content Type |
Thesis or Dissertation
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Description | T cell activation is tightly regulated by both stimulatory and inhibitory co-receptors and has been a focus in the development of interventions for managing cancer or autoimmune diseases. Targeting the inhibitory co-receptors programmed cell death 1 (PD-1) and cytotoxic T lymphocyte–associated protein 4 (CTLA-4) has successfully eradicated tumors but induced immune-related adverse events in humans and mice. The beneficial and adverse effects of targeting these co-receptors highlight their importance in cancer immunity and also autoimmunity. Although the therapeutic potencies of other inhibitory co-receptors are under extensive investigation, their inhibitory mechanisms and their functional differences are not well understood. Here we analyzed the inhibitory mechanisms of lymphocyte activation gene-3 (LAG-3), another inhibitory co-receptor, by using an in vitro T cell activation system and a high-affinity anti-LAG-3 antibody that strongly interferes with the binding of LAG-3 to its ligand. We found that the expression level of LAG-3 strongly correlates with the inhibitory function of LAG-3, suggesting that LAG-3 functions as a rheostat rather than as a breaker of T cell activation. By evaluating the inhibitory capacities of various LAG-3 variants relative to their expression levels, we found that LAG-3 transduces two independent inhibitory signals through an FXXL motif in the membrane-proximal region and the C-terminal EX repeat. These motifs have not been reported previously for inhibitory co-receptors, suggesting that LAG-3 inhibits T cell activation through a nonredundant inhibitory mechanisms along with the other inhibitory co-receptors. Our findings provide a rationale for combinatorial targeting of LAG-3 and the other inhibitory co-receptors to improve cancer immunotherapy.
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Journal Title |
Journal of Biological Chemistry
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ISSN | 1083351X
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NCID | AA1202441X
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Publisher | American Society for Biochemistry and Molecular Biology
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Volume | 294
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Issue | 15
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Start Page | 6017
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End Page | 6026
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Published Date | 2019-02-13
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Remark | 内容要旨・審査要旨・論文本文の公開
本論文は,著者Takeo K. Maedaの学位論文として提出され,学位審査・授与の対象となっている。 This research was originally published in the Journal of Biological Chemistry. Takeo K. Maeda, Daisuke Sugiura, Il-mi Okazaki, Takumi Maruhashi, Taku Okazaki. Atypical motifs in the cytoplasmic region of the inhibitory immune co-receptor LAG-3 inhibit T cell activation. J. Biol. Chem. 2019 Vol.294(15), pp.6017-6026. |
Rights | © 2019 Maeda et al. Published under exclusive license by The American Society for Biochemistry and Molecular Biology, Inc.
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EDB ID | |
DOI (Published Version) | |
URL ( Publisher's Version ) | |
FullText File | |
language |
eng
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TextVersion |
ETD
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MEXT report number | 甲第3319号
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Diploma Number | 甲医第1421号
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Granted Date | 2019-06-27
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Degree Name |
Doctor of Medical Science
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Grantor |
Tokushima University
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departments |
Institute of Advanced Medical Sciences
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