Antitumor and cytotoxic properties of a humanized antibody specific for the GM3(Neu5Gc) ganglioside

被引:12
|
作者
Dorvignit, Denise [1 ]
Garcia-Martinez, Liliana [1 ]
Rossin, Aurelie [2 ]
Sosa, Katya [1 ]
Viera, Justo [3 ]
Hernandez, Tays [1 ]
Mateo, Cristina [4 ]
Hueber, Anne-Odile [2 ]
Mesa, Circe [1 ]
Lopez-Requena, Alejandro [1 ]
机构
[1] Ctr Mol Immunol, Immunobiol Direct, Havana 11600, Cuba
[2] Inst Biol Valrose, Nice, France
[3] Ctr Mol Immunol, Syst Biol Direct, Havana 11600, Cuba
[4] Ctr Mol Immunol, Innovat Direct, Havana 11600, Cuba
关键词
GM3(Neu5Gc) ganglioside; Necrosis; Apoptosis; Antibody dependent cell-mediated; cytotoxicity; Antitumor effect; N-GLYCOLYLNEURAMINIC ACID; MITOCHONDRIAL-MEMBRANE PERMEABILIZATION; ANTIGANGLIOSIDE GM2 ANTIBODY; 14F7; MONOCLONAL-ANTIBODY; CANCER-THERAPY; CELL-DEATH; IN-VIVO; PHOSPHATIDYLSERINE EXPOSURE; BREAST-CANCER; APOPTOSIS;
D O I
10.1016/j.imbio.2015.07.008
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Gangliosides are sialic acid-bearing glycosphingolipids expressed on all mammalian cell membranes, and participate in several cellular processes. During malignant transformation their expression changes, both at the quantitative and qualitative levels. Of particular interest is the overexpression by tumor cells of Neu5Gc-gangliosides, which are absent, or detected in trace amounts, in human normal cells. The GM3(Neu5Gc) ganglioside in particular has been detected in many human tumors, and it is considered one of the few tumor specific antigen. We previously demonstrated that a humanized antibody specific for this molecule, named 14F7hT, retained the binding and cytotoxic properties of the mouse antibody. In this work, we confirm that 14F7hT exerts a non-apoptotic cell death mechanism in vitro and shows its potent in vivo antitumor activity on a solid mouse myeloma model. Also, we demonstrate, in contrast to the murine counterpart, the capacity of this antibody to induce antibody-dependent cell-mediated cytotoxicity using human effector cells, which increases its potential for the treatment of GM3(Neu5Gc)expressing human tumors. (C) 2015 Elsevier GmbH. All rights reserved.
引用
收藏
页码:1343 / 1350
页数:8
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