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. 2021 Dec 14;11(12):202. doi: 10.1038/s41408-021-00594-1

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© The Author(s) 2021

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. 2 — A Supervised clustering of 83 patients with hematological malignancies and 102 health care practitioners (HCP), based on the percentile distribution of 59 immune cell types in peripheral blood that were categorized into five groups: granulocytes, antigen-presenting cells (APC), CD4, and CD8 T cells and B cells. Patients were grouped based on the diagnosis of a B-cell lymphoproliferative disorder (B-cell dis.), monoclonal gammopathies (MG), and Hodgkin lymphoma (HL). B Statistical significance of differences across groups (with graphical representation of such differences in Supplemental Fig. 2). CM, central memory; EM, effector memory; Treg, T regulatory cells; Tfh, T follicular-like; TEMRA, terminally effector memory CD45RA+; PC, plasma cells. *P < 0.05; **P < 0.01; ***P < 0.001; n.s., not significant.