Figure 5
Figure 5. In vivo fate mapping by TCR clonotyping uncovers the differentiation landscapes of TN after transplant. (A) Graphic representation of the distribution within day 30 memory T-cell subsets of the TCRB sequences harbored by a given T-cell subset from LP. Numbers in donut graphs indicate the average percentages, from the 3 patients analyzed, of TCRB sequences retrieved in the indicated memory subsets 30 days after HSCT. (B) Quantification of the expansion ability of single-cell progenies of T lymphocytes with a given phenotype within LP, independent of the memory T-cell subset in which they were retrieved at day 30 post-HSCT. Expansion is measured as fold change of TCRB sequence count at day 30 relative to LP from a representative patient (UPN#12). (C) Circos plot16 graphically summarizes the distribution of TCRB sequences originally harbored by LP-TN in a representative patient (UPN#12) of the 3 analyzed. LP-TN sequences are depicted in the bottom part of the circle, identified by the green band. From each LP-TN-derived TCRB sequence departs a ribbon connecting it to 1 or more memory subsets at day 30 post-HSCT. Each day 30 memory subset is denoted by a colored band (red for TSCM, orange for TCM, and blue for TEM/EFF). Ribbon thickness is proportional to the TCRB sequence count of the given clonotype at day 30 post-HSCT. (D) Left pie chart shows the distribution at day 30 after transplant of the TCRB sequences originally harbored by LP-TN. Numbers in the pie indicate the average percentages from the 3 patients analyzed; right chart zooms on the fraction of clonotypes that were found shared among 2 or more subsets at day 30 post-HSCT and depicts the mean distribution of all combinations retrieved. (E) Spearman correlation heat map representing the contribution of individual LP-TN-derived clonotypes (row) to the repertoire of TSCM, TCM, and TEM/EFF subsets at day 30 post-HSCT (columns). The analysis is performed to LP-TN TCRB sequences that are shared by at least 2 memory T-cell subsets at day 30 post-HSCT. (F) Box plots quantify the expansion, measured as count fold change relative to LP, of LP-TN TCRB sequences that were retrieved in memory T-cell subsets at day 30 post-HSCT. (G) Model scheme of a proposed branched diversification pathway from TN to TSCM, TCM, and TEM/EFF subsets on in vivo transfer after HSCT.

In vivo fate mapping by TCR clonotyping uncovers the differentiation landscapes of TN after transplant. (A) Graphic representation of the distribution within day 30 memory T-cell subsets of the TCRB sequences harbored by a given T-cell subset from LP. Numbers in donut graphs indicate the average percentages, from the 3 patients analyzed, of TCRB sequences retrieved in the indicated memory subsets 30 days after HSCT. (B) Quantification of the expansion ability of single-cell progenies of T lymphocytes with a given phenotype within LP, independent of the memory T-cell subset in which they were retrieved at day 30 post-HSCT. Expansion is measured as fold change of TCRB sequence count at day 30 relative to LP from a representative patient (UPN#12). (C) Circos plot16  graphically summarizes the distribution of TCRB sequences originally harbored by LP-TN in a representative patient (UPN#12) of the 3 analyzed. LP-TN sequences are depicted in the bottom part of the circle, identified by the green band. From each LP-TN-derived TCRB sequence departs a ribbon connecting it to 1 or more memory subsets at day 30 post-HSCT. Each day 30 memory subset is denoted by a colored band (red for TSCM, orange for TCM, and blue for TEM/EFF). Ribbon thickness is proportional to the TCRB sequence count of the given clonotype at day 30 post-HSCT. (D) Left pie chart shows the distribution at day 30 after transplant of the TCRB sequences originally harbored by LP-TN. Numbers in the pie indicate the average percentages from the 3 patients analyzed; right chart zooms on the fraction of clonotypes that were found shared among 2 or more subsets at day 30 post-HSCT and depicts the mean distribution of all combinations retrieved. (E) Spearman correlation heat map representing the contribution of individual LP-TN-derived clonotypes (row) to the repertoire of TSCM, TCM, and TEM/EFF subsets at day 30 post-HSCT (columns). The analysis is performed to LP-TN TCRB sequences that are shared by at least 2 memory T-cell subsets at day 30 post-HSCT. (F) Box plots quantify the expansion, measured as count fold change relative to LP, of LP-TN TCRB sequences that were retrieved in memory T-cell subsets at day 30 post-HSCT. (G) Model scheme of a proposed branched diversification pathway from TN to TSCM, TCM, and TEM/EFF subsets on in vivo transfer after HSCT.

Close Modal

or Create an Account

Close Modal
Close Modal