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. 2022 Feb 17;28(8):1572–1585. doi: 10.1158/1078-0432.CCR-21-3324

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©2022 The Authors; Published by the American Association for Cancer Research

This open access article is distributed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0) license.

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Figure 7. Immune cells were isolated from cerebrospinal fluid at indicated timepoints after Delta24-RGD infusion and analyzed by flow cytometry with the following markers: CD45+CD3−CD56+ (NK cells), DCs (CD45+/lineage−/HLA-DR+), CD45+CD3+/CD4+ (CD4+ T-lymphocytes), and CD45+CD3+/CD8+ (CD8+ T-lymphocytes). Immune cell subsets are presented as absolute numbers per μL CSF. Gray-shaded areas indicate the normal range for each cell type. — Immune cells were isolated from cerebrospinal fluid at indicated timepoints after Delta24-RGD infusion and analyzed by flow cytometry with the following markers: CD45⁺CD3⁻CD56⁺ (NK cells), DCs (CD45⁺/lineage⁻/HLA-DR⁺), CD45⁺CD3⁺/CD4⁺ (CD4⁺ T-lymphocytes), and CD45⁺CD3⁺/CD8⁺ (CD8⁺ T-lymphocytes). Immune cell subsets are presented as absolute numbers per μL CSF. Gray-shaded areas indicate the normal range for each cell type.