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. Author manuscript; available in PMC: 2022 May 26.
Published in final edited form as: J Allergy Clin Immunol. 2021 Aug 9;149(3):1113–1119. doi: 10.1016/j.jaci.2021.07.029

FIG 1.

FIG 1.

A, Representative hierarchical tree maps showing increasing TRB repertoire diversity following successful HCT in patient 18 (P18, top row) and failed HCT in patient 10, treatment A (P10, bottom row). (B) Increasing Shannon [H] index of TRB diversity and (C) Simpson [1-D] index of clonality in all patient cellular treatments over time. The P values refer to differences between 3 and 6 months post-HCT. D, Persistently lower Shannon diversity scores following cellular treatments that ultimately needed another treatment (black squares) compared with those that were successful (red circles); differences were apparent as soon as 3 months after cellular treatments. The P value refers to the differences between the 2 groups considering all time points. E, Correlation (Spearman rank coefficient Rs) between naive CD4+ T-cell number and Shannon [H] index of diversity 6 months after a cellular treatment. F, Relationship between TCR diversity and genotype groupings (IL2RG, IL7R, and JAK3, black circles; RAG and DCLRE1C, red squares). The number of samples available at the 3-month time point was insufficient to assess whether the difference between the 2 groups was significant (only 1 sample was available for the RAG/DCLRE1C group at 3 months). In Fig 1, B-D and F, symbols and bars correspond to mean ± SEM.