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. 2020 Dec 10;17:194. doi: 10.1186/s12985-020-01465-0

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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/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

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Fig. 4 — A/WSN/1933 virus-specific antibody production by C57BL/6J wild type mice and CD83 KO mice after intraperitoneal injection of A/WSN/1933 virus. Peritoneal cavity fluids and sera were collected at 5, 7, and 14 days after intraperitoneal injection of live A/WSN/1933 virus in mice (n = 5/group) with a dose of 5 × 10⁶ pfu/mice. The amount of total IgG and IgG subclasses were quantified by ELISA. a A/WSN/1933 virus-specific antibody production in the peritoneal cavity fluid. b A/WSN/1933 virus-specific antibody production in sera. ***P < 0.001