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. 2021 Dec 16;22:76. doi: 10.1186/s12865-021-00466-0

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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. 2 — Comparison of lymphocyte and CD4 + T cell subset percentages among the RA-CAD (n = 54), pure RA (n = 43), and HC (n = 43) groups. A The percentages of B, NK, CD3 + T, CD4 + T, and CD8 + T cells in RA-CAD patients, pure RA patients, and healthy controls. B The percentages of Th1, Th2, Th17, and Treg cells in RA-CAD patients, pure RA patients, and healthy controls. Data are medians (Q25,Q75) and were compared using the Mann–Whitney U test between each of the two groups. *p < 0.05; **p < 0.01; ***p < 0.001