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. 2023 Aug 31;29(9):2295–2306. doi: 10.1038/s41591-023-02491-5

Fig. 3. Monoallelic TNFRSF17 deletion coupled with p.Arg27Pro mutation in the extracellular domain of BCMA mediates MM relapse after anti-BCMA TCE therapy in patient MM-3.

Fig. 3

a, Pre-therapy versus post-relapse CD138+ MM cell BCMA protein expression by flow cytometry using monoclonal anti-BCMA antibody (clone 19F2). b, Pre-therapy versus post-relapse CD138+ BCMA protein expression level by flow cytometry using polyclonal anti-BCMA antibody. c, ScCNV-seq heatmap comparing the CN changes in chromosomes 1–22 in pre-therapy (pre) versus post-relapse (post) CD138+ MM cells. d, Pre-therapy and post-relapse CD138+ CN alteration at the TNFRSF17 locus based on scCNV-seq. The barplot and table compare the percentages of cells harboring the CNVs in pre- versus post-CAR T/TCE relapse samples. e, Lollipop plot illustrating the 11965404G>C mutation in exon 1 of the TNFRSF17 gene. Integrated Genomics Viewer (IGV) screenshot illustrating newly detected clonal point mutation in post-relapse CD138+ MM cells. f, Fish plot of clonal phylogeny of the CD138+ cells at pre-therapy versus post-relapse timepoints inferred from scCNV-seq data. The associated phylogenetic tree illustrates the main alterations differentiating each clone.