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  • Poster presentation
  • Open Access

Characterization of tumor infiltrated cells in mouse model

  • 1,
  • 1 and
  • 1
Journal for ImmunoTherapy of Cancer20153(Suppl 2):P407

https://doi.org/10.1186/2051-1426-3-S2-P407

Published: 4 November 2015

Keywords

  • Myeloid Cell
  • Lymphoid Cell
  • Suppressor Cell
  • Cancer Immunotherapy
  • Lineage Marker

Solid tumors show a trend to develop immunosuppressive microenvironment and a dynamic cell composition along tumor progression. Various types of non-immune and immune cells constitute solid tumor. Understanding the change of cellular constituents and their function is pertinent to understand tumor immune status, which enables rational design of cancer immunotherapy. Given the complexity of tumor infiltrating cells, the identification of each cellular component still remains controversial. In this study, we characterized the immune cells in B16F10 and E0771 tumor. In respect of lymphoid cells, the proportion and functional phenotypes of T cell, B cell, NK cell, NKT cell and innate lymphoid cell were examined. Myeloid cell populations, such as granulocyte, macrophage, dendritic cell and myeloid-derived suppressor cell, were identified by updated myeloid lineage markers. Together with previous studies, the immune profile of B16F10 and E0771 tumor is better understood.

Authors’ Affiliations

(1)
Academia Sinica, Taipei, Taiwan

Copyright

© Liou et al. 2015

This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. 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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