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. 2023 Nov 27;38(2):340–350. doi: 10.1038/s41375-023-02093-7

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© The Author(s) 2023

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 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/.

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Fig. 7 — A UMAP plots of LN B cell subclusters. Cells are shown separately for each clinical status (right panels). FCRL4⁺ MBC, FCRL4-positive memory B cell; GCB (DZ), germinal center B cell in the dark zone; GCB (LZ), GCB in the light zone; MBC, memory B cell; NBC, naïve B cell; PBL, plasmablast; PC, plasma cell; preGCB, pre-germinal center B cell. B Clone size of BCRs in B cells from AITL5LN, AITL9LN, and HLNs. The number of cells expressing each clonotype was defined as clone size and calculated for each sample. HLN samples are shown as integrated (right). C BCR overlap analysis of B cells from AITL5LN, AITL9LN, and HLNs. AITL5LN and AITL9LN were analyzed individually while HLN samples were analyzed after integration.