Human T cell glycosylation and implications on immune therapy for cancer

被引:34
作者
De Bousser, Elien [1 ,2 ]
Meuris, Leander [1 ,2 ]
Callewaert, Nico [1 ,2 ]
Festjens, Nele [1 ,2 ]
机构
[1] VIB UGent Ctr Med Biotechnol, Ghent, Belgium
[2] Univ Ghent, Biochem & Microbiol Dept, Ghent, Belgium
关键词
Glycosylation; human T cell; immunotherapy; glycan-binding protein; engineering; N-ACETYLGLUCOSAMINYLTRANSFERASE; PROTEIN GLYCOSYLATION; SYSTEMS GLYCOBIOLOGY; P-SELECTIN; GLYCANS; ACTIVATION; GALECTIN-3; BINDING; SIALYLATION; EXPRESSION;
D O I
10.1080/21645515.2020.1730658
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Glycosylation is an important post-translational modification, giving rise to a diverse and abundant repertoire of glycans on the cell surface, collectively known as the glycome. When focusing on immunity, glycans are indispensable in virtually all signaling and cell-cell interactions. More specifically, glycans have been shown to regulate key pathophysiological steps within T cell biology such as T cell development, thymocyte selection, T cell activity and signaling as well as T cell differentiation and proliferation. They are of major importance in determining the interaction of human T cells with tumor cells. In this review, we will describe the role of glycosylation of human T cells in more depth, elaborate on the importance of glycosylation in the interaction of human T cells with tumor cells and discuss the potential of cancer immunotherapies that are based on manipulating the glycome functions at the tumor immune interface.
引用
收藏
页码:2374 / 2388
页数:15
相关论文
共 125 条
[1]   Profiling of Protein O-GIcNAcylation in Murine CD8+ Effector- and Memory-like T Cells [J].
Aguilar, Aime Lopez ;
Gao, Yu ;
Hou, Xiaomeng ;
Lauvau, Gregoire ;
Yates, John R. ;
Wu, Peng .
ACS CHEMICAL BIOLOGY, 2017, 12 (12) :3031-3038
[2]   Enhancement of CD8 T-cell function through modifying surface glycoproteins in young and old mice [J].
Akha, Amir A. Sadighi ;
Berger, Scott B. ;
Miller, Richard A. .
IMMUNOLOGY, 2006, 119 (02) :187-194
[3]   T-cell regulation by CD28 and CTLA-4 [J].
Alegre, ML ;
Frauwirth, KA ;
Thompson, CB .
NATURE REVIEWS IMMUNOLOGY, 2001, 1 (03) :220-228
[4]   The ST6Gal I sialyltransferase selectively modifies N-glycans on CD45 to negatively regulate galectin-1-induced CD45 clustering, phosphatase modulation, and T cell death [J].
Amano, M ;
Galvan, M ;
He, JL ;
Baum, LG .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (09) :7469-7475
[5]   Determination of glycosylation sites and site-specific heterogeneity in glycoproteins [J].
An, Hyun Joo ;
Froehlich, John W. ;
Lebrilla, Carlito B. .
CURRENT OPINION IN CHEMICAL BIOLOGY, 2009, 13 (04) :421-426
[6]   Search-and-replace genome editing without double-strand breaks or donor DNA [J].
Anzalone, Andrew V. ;
Randolph, Peyton B. ;
Davis, Jessie R. ;
Sousa, Alexander A. ;
Koblan, Luke W. ;
Levy, Jonathan M. ;
Chen, Peter J. ;
Wilson, Christopher ;
Newby, Gregory A. ;
Raguram, Aditya ;
Liu, David R. .
NATURE, 2019, 576 (7785) :149-+
[7]   Glycolysis and glutaminolysis cooperatively control T cell function by limiting metabolite supply to N-glycosylation [J].
Araujo, Lindsey ;
Khim, Phillip ;
Mkhikian, Haik ;
Mortales, Christie-Lynn ;
Demetriou, Michael .
ELIFE, 2017, 6
[8]   Characterization of terminal sialic acid linkages on human thymocytes - Correlation between lectin-binding phenotype and sialyltransferase expression [J].
Baum, LG ;
Derbin, K ;
Perillo, NL ;
Wu, T ;
Pang, M ;
Uittenbogaart, C .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (18) :10793-10799
[9]   The direct and indirect effects of glycans on immune function [J].
Baum, Linda G. ;
Cobb, Brian A. .
GLYCOBIOLOGY, 2017, 27 (07) :619-624
[10]   Selectins in cancer immunity [J].
Borsig, Lubor .
GLYCOBIOLOGY, 2018, 28 (09) :648-655