Galectin-1 research in T cell immunity: Past, present and future

被引:128
作者
Cedeno-Laurent, Filiberto [1 ,2 ]
Dimitroff, Charles J. [1 ,2 ]
机构
[1] Brigham & Womens Hosp, Dept Dermatol, Boston, MA 02115 USA
[2] Harvard Univ, Sch Med, Boston, MA 02115 USA
关键词
Galectin-1; ligands; Immunoregulation; Cancer immune evasion; Carbohydrate therapeutics; Immunotherapy; GALACTOSIDE-BINDING LECTIN; HAMSTER OVARY CELLS; CORE-2; O-GLYCANS; REGULATORY CELLS; PERIPHERAL-BLOOD; SURFACE EXPOSURE; DENDRITIC CELLS; STROMAL CELLS; BREAST-CANCER; CUTTING EDGE;
D O I
10.1016/j.clim.2011.09.011
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
071005 [微生物学]; 100108 [医学免疫学];
摘要
Galectin-1 (Gal-1) is one of 15 evolutionarily conserved B-galactoside-binding proteins that display biologically-diverse activities in pathogenesis of inflammation and cancer. Gal-1 is variably expressed on immune cells and endothelial cells, though is commonly found and secreted at high levels in cancer cells. It induces apoptosis in effector T cells through homodimeric binding of N-acetyllactosamines on membrane glycoproteins (Gal-1 ligands). There is also compelling evidence in models of cancer and autoimmunity that recombinant Gal-1 (rGal-1) can potentiate immunoregulatory function of T cells. Here, we review Gal-1's structural and functional features, while analyzing potential drawbacks and technical difficulties inherent to rGal-1's nature. We also describe new Gal-1 preparations that exhibit dimeric stability and functional activity on T cells, providing renewed excitement for studying Gal-1 efficacy and/or use as anti-inflammatory therapeutics. We lastly summarize strategies targeting the Gal-1 Gal-1 ligand axis to circumvent Gal-1-driven immune escape in cancer and boost anti-tumor immunity. (C) 2011 Elsevier Inc. All rights reserved.
引用
收藏
页码:107 / 116
页数:10
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