Please use this identifier to cite or link to this item: https://doi.org/10.1038/srep34310
Title: CD16 is indispensable for antibodydependent cellular cytotoxicity by human monocytes
Authors: Yeap, W.H
Wong, K.L
Shimasaki, N 
Teo, E.C.Y
Quek, J.K.S
Yong, H.X
Diong, C.P
Bertoletti, A 
Linn, Y.C 
Wong, S.C
Issue Date: 2016
Citation: Yeap, W.H, Wong, K.L, Shimasaki, N, Teo, E.C.Y, Quek, J.K.S, Yong, H.X, Diong, C.P, Bertoletti, A, Linn, Y.C, Wong, S.C (2016). CD16 is indispensable for antibodydependent cellular cytotoxicity by human monocytes. Scientific Reports 6 : 34310. ScholarBank@NUS Repository. https://doi.org/10.1038/srep34310
Rights: Attribution 4.0 International
Abstract: Antibody dependent cellular cytotoxicity (ADCC) is exerted by immune cells expressing surface Fc? receptors (Fc?Rs) against cells coated with antibody, such as virus infected or transformed cells. CD16, the Fc?RIIIA, is essential for ADCC by NK cells, and is also expressed by a subset of human blood monocytes. We found that human CD16- expressing monocytes have a broad spectrum of ADCC capacities and can kill cancer cell lines, primary leukemic cells and hepatitis B virus infected cells in the presence of specific antibodies. Engagement of CD16 on monocytes by antibody bound to target cells activated ?2 integrins and induced TNF? secretion. In turn, this induced TNFR expression on the target cells, making them susceptible to TNF? mediated cell death. Treatment with TLR agonists, DAMPs or cytokines, such as IFN?, further enhanced ADCC. Monocytes lacking CD16 did not exert ADCC but acquired this property after CD16 expression was induced by either cytokine stimulation or transient transfection. Notably, CD16+ monocytes from patients with leukemia also exerted potent ADCC. Hence, CD16+ monocytes are important effectors of ADCC, suggesting further developments of this property in the context of cellular therapies for cancer and infectious diseases. © The Author(s) 2016.
Source Title: Scientific Reports
URI: https://scholarbank.nus.edu.sg/handle/10635/178861
ISSN: 20452322
DOI: 10.1038/srep34310
Rights: Attribution 4.0 International
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