共 88 条
Galectin-1 research in T cell immunity: Past, present and future
被引:128
作者:

Cedeno-Laurent, Filiberto
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h-index: 0
机构:
Brigham & Womens Hosp, Dept Dermatol, Boston, MA 02115 USA
Harvard Univ, Sch Med, Boston, MA 02115 USA Brigham & Womens Hosp, Dept Dermatol, Boston, MA 02115 USA

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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.
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页码:107 / 116
页数:10
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