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. 2020 Jun 5;11:2856. doi: 10.1038/s41467-020-16625-7

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© The Author(s) 2020

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. 10 — Data from Fig. 9 indicate that IFN-I stimulates the expression of IL-6 and IL-12p40 from activated B cells which, in the context of auto-antigen, supports the proliferation of inflammatory TH17 cells. In contrast, IFN-I stimulation of naive B cells elevates IL-10 and not IL-6 and does not efficiently promote inflammatory TH17 cell proliferation.