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. 2022 Oct 28;13:6439. doi: 10.1038/s41467-022-33832-6

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© The Author(s) 2022

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

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Fig. 7 — a Quantification of MeV eGFP positive cells in indicated PBMC subpopulations by flow cytometry: CD14⁺ monocytes, CD4⁺, CD8⁺ and CD20⁺ lymphocytes in MeV-infected cynomolgus monkeys by flow cytometry, following the nebulization of either 0.9% NaCl (C) or HRC4 peptide (P). CD4⁺ T lymphocytes were characterized as CD3⁺CD8^-, and CD8⁺ T lymphocytes were characterized as CD3⁺/CD8⁺; B-lymphocytes were characterized as CD3^-/CD20⁺ cells. b Analysis of the contribution of each lymphocyte subpopulation among infected PBMCs; results are presented as the percentage of each analyzed cell population among the infected cells on the day of peak of MeV infection (day 6 for C3 and day 9 for C1 and P2; C2 is not displayed due to a low number of infected cells). Numbers below the graphs correspond to the number of analyzed cells for each presented animal. Data were acquired on a MACSQuant® 10 flow cytometer (Miltenyi). Source data are provided as a Source Data file.