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. 2021 Oct 27;10(11):e1351. doi: 10.1002/cti2.1351

Figure 1.

Figure 1

The TCR repertoires in DLBCL diagnostic biopsies stratified by iPET status. (a) Cumulative frequency of the most abundant 100 intratumoral TCR clonotypes (CumFreq‐100), (b) cumulative frequency of the most abundant 25 intratumoral TCR clonotypes (CumFreq‐25), (c) the productive clonality in the intratumoral TCR repertoire and (d) the productive clonality after downsizing by random drawing. In iPET+ patients, the CumFreq‐100 and CumFreq‐25 were higher suggesting a stronger level of oligoclonal expansion by high‐frequency clonotypes. The resulting high productive clonality was suggestive of lower clonotype diversity.