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. 2019 Aug 19;19:817. doi: 10.1186/s12885-019-6034-1

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© The Author(s). 2019

Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

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Fig. 3 — Functional receptor expression and cytokine production of MYJ1633. (a) The expression of activating, natural cytotoxicity, and inhibiting receptors on CD16⁺ CD56⁺ MYJ1633 was determined by using flow cytometry. The data was analyzed from 6 individuals (Additional file 1: Figure S2). The data represented as mean ± SEM. (b) IFN-γ and (c) TNF-α levels in cell culture supernatants of PBMCs and MYJ1633 were quantitatively measured using sandwich ELISA system. Significant differences between PBMC and MYJ1633 from 6 individuals were determined by Student’s t test. The mean value of each group is indicated with red bars