monocyte cytotoxicity
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2009 ◽  
Vol 27 (4) ◽  
pp. 271-278 ◽  
Author(s):  
Knud Kragballe ◽  
Johan Lanng Nielsen ◽  
Jacob Sølling ◽  
Jørgen Ellegaard

2000 ◽  
Vol 192 (9) ◽  
pp. 1373-1380 ◽  
Author(s):  
Masafumi Nakayama ◽  
Nobuhiko Kayagaki ◽  
Noriko Yamaguchi ◽  
Ko Okumura ◽  
Hideo Yagita

TWEAK, a new member of the tumor necrosis factor (TNF) family, induces cell death in some tumor cell lines, but its physiological functions are largely unknown. In this study, we investigated the expression and function of TWEAK in human peripheral blood mononuclear cells (PBMCs) by using newly generated anti–human TWEAK mAbs. Although freshly isolated PBMCs expressed no detectable level of TWEAK on their surfaces, a remarkable TWEAK expression was rapidly observed on monocytes upon stimulation with interferon (IFN)-γ but not with IFN-α or lipopolysaccharide. Cytotoxic activity of IFN-γ–stimulated monocytes against human squamous carcinoma cell line HSC3 was inhibited partially by anti-TWEAK mAb alone and almost completely by combination with anti-TRAIL (TNF-related apoptosis-inducing ligand) mAb. These results revealed a novel pathway of monocyte cytotoxicity against tumor cells that is mediated by TWEAK and potentiated by IFN-γ.


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