Blockage of Core Fucosylation Reduces Cell-Surface Expression of PD-1 and Promotes Anti-tumor Immune Responses of T Cells
Summary: Programmed cell death 1 (PD-1) is highly expressed on exhausted T cells and inhibits T cell activation. Antibodies that block the interaction between PD-1 and its ligand prevent this inhibitory signal and reverse T cell dysfunction, providing beneficial anti-tumor responses in a substantial...
Main Authors: | Masahiro Okada, Shunsuke Chikuma, Taisuke Kondo, Sana Hibino, Hiroaki Machiyama, Tadashi Yokosuka, Miyako Nakano, Akihiko Yoshimura |
---|---|
Format: | Article |
Language: | English |
Published: |
Elsevier
2017-08-01
|
Series: | Cell Reports |
Online Access: | http://www.sciencedirect.com/science/article/pii/S2211124717309932 |
Similar Items
-
Core Fucosylation of the T Cell Receptor Is Required for T Cell Activation
by: Wei Liang, et al.
Published: (2018-01-01) -
Single-cell fucosylation breakdown: Switching fucose to europium
by: Zhen Liu, et al.
Published: (2021-05-01) -
Evaluation of therapeutic PD-1 antibodies by an advanced single-molecule imaging system detecting human PD-1 microclusters
by: Wataru Nishi, et al.
Published: (2023-06-01) -
Memory T cell, exhaustion, and tumor immunity
by: Makoto Ando, et al.
Published: (2020-01-01) -
Targeting abatacept-resistant T-helper-17 cells by aldehyde dehydrogenase inhibition
by: By Yukiko Tokifuji, et al.
Published: (2024-01-01)