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. 2019 Feb 18;12:18. doi: 10.1186/s13045-019-0704-y

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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. 7 — Infiltration of M28z10 T cells into GC tissue is enhanced by peritumoral delivery. a Schematic representation of the experiments. b Tumor weight of BGC-823 subcutaneously injected mice with different T cell delivery methods when sacrificed at each different time point. Error bars denote the s.e.m., and the results were compared with two-way ANOVA test. *P < 0.05; **P < 0.01; ***P < 0.001. c Representative Immunofluorescence imaging of the tumor tissue section for the BGC-823 s.c. mice with different T cell delivery methods sacrificed in day29, scale bar = 20 μm. d Detection of the percentage of tumor infiltrated T cells by FACS. Error bars denote the s.e.m., and the results were compared with two-way ANOVA test. *P < 0.05; **P < 0.01; ***P < 0.001