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. 2016 Dec 9;11(12):e0165118. doi: 10.1371/journal.pone.0165118

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© 2016 Zhang et al

This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

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Fig 1 — The frequency of different immune subsets was evaluated in brain, blood and spleen during progression of intracranial GL261 gliomas over a three-week period. A) Flow cytometry analysis of CD11b⁺CD45⁺ myeloid cells and CD11b⁺Gr1⁺ (marker of myeloid derived suppressor cells). B) Flow cytometry analysis of CD4⁺CD25⁺Foxp3⁺ and C) CD8⁺ T and NK cell. Data is representative of two separate experiments. n = 3 mice/group ± SD.