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. 2021 Jan 18;14:54. doi: 10.1186/s13071-020-04541-0

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© The Author(s) 2021

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. 1 — Peritoneal lymphocyte cell population in the peritoneal cavities of healthy and Mesocestoides vogae-infected mice at 3, 6, 10, 14, 19, 25, 30 and 35 days post-infection. Peritoneal exudate cells were isolated from the peritoneal cavity, and the expression of lymphocyte surface markers by these cells was analyzed from lymphogate using flow cytometry. a Representative dot plots show the expression of CD3/CD19, CD4/CD8 and CD49b/CD8 on PEC. Proportions of T- and B-lymphocytes (b), T-lymphocyte subpopulations (c), NK and NKT cells (d) in the peritoneal cavities of healthy and infected mice. Data are expressed as the means ± SD. Statistical significance was analyzed using one-way ANOVA with Dunnett's post-test, and significantly different values between control and infected groups are indicated as: *p < 0.05, **p < 0.01, ***p < 0.001.