Cedeno-Laurent F, Watanabe R, Teague JE et al.Galectin-1 inhibits the viability, proliferation, and Th1 cytokine production of nonmalignant T cells in patients with leukemic cutaneous T-cell lymphoma. Blood 119:3534-3538

Department of Dermatology, Brigham and Women's Hospital, Boston, MA, USA.
Blood (Impact Factor: 10.45). 03/2012; 119(15):3534-8. DOI: 10.1182/blood-2011-12-396457
Source: PubMed


Tumor-derived galectin-1 (Gal-1), a β-galactoside-binding S-type lectin, has been shown to encourage T-cell death and promote T cell-mediated tumor immune escape. In this report, we show that patients with leukemic cutaneous T-cell lymphomas, known to have limited complexity of their T-cell repertoires, have a predominant T helper type-2 (Th2) cytokine profile and significantly elevated plasma levels of Gal-1 compared with healthy controls. Circulating clonal malignant T cells were a major source of Gal-1. The conditioned supernatant of cultured malignant T cells induced a β-galactoside-dependent inhibition of normal T-cell proliferation and a Th2 skewing of cytokine production. These data implicate Gal-1 in development of the Th2 phenotype in patients with advanced-stage cutaneous T-cell lymphoma and highlight the Gal-1-Gal-1 ligand axis as a potential therapeutic target for enhancing antitumor immune responses.

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    • "Galectins, a family of S-type lectins found in a large scale of species, are characterized by two features: a specific affinity for β-galactoside and a conserved specific sequence motif called carbohydrate recognition domain (CRD) [1]. To date, 15 mammalian galectins (galectin-1 to -15) have been cloned and functionally characterized [2], revealing various roles in apoptosis [3], chemo-attraction [4], cell adhesion [5], cell proliferation [5], cytokine secretion [6] and immune responses [7]. After the discovery of the first nematode tandem repeat type galectin in Caenorhabditis elegans (C. "
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