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. 2020 Apr 23;78(2):661–673. doi: 10.1007/s00018-020-03517-8

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© The Author(s) 2020

Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/.

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Fig. 5 — MAF maintain increased expression of the immune checkpoint regulators HVEM and VISTA. Comparative analysis of cell surface Herpesvirus entry mediator (HVEM), Galectin-3, Galectin-9, Programmed death-ligand 1 (PD-L1), CD155 (poliovirus receptor) and V-domain Ig suppressor of T cell activation (VISTA) expression (mean fluorescence intensity) on MAF and DF cells, as analyzed by flow cytometry (n = 6 Mann–Whitney U test BTLA p = 0.029 and HVEM p = 0.0311). Data from three independent experiments