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. 2022 Jun 25;19:106. doi: 10.1186/s12985-022-01842-x

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© The Author(s) 2022

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. 2 — Proliferation of immunized BALB/c mice splenocytes after in vitro re-stimulation with synthetic E7 specific epitope. Splenocytes from mice were harvested one week after the last immunization, and MTT assay evaluated lymphocyte proliferation. Results represent the mean ± SD of 3 mice per groups. ***Statistically significant differences between the E7 DNA plus IL-24 adjuvant compared with other groups (E7 DNA, IL-24, pcDNA, PBS) as determined by one-way ANOVA (P < 0.001)