Figure 4.
Figure 4. Intraclonal heterogeneity for CD158k and TCR Vβ expression in patients 1 and 13 and cell sorting analysis. (Ai) Patient 13 showed 2 distinct TCRαβdim and TCRαβbright circulating T-cell populations. Two-color flow cytometry showed that CD158k+ cells were present within both T-cell populations. (Aii) GeneScan Analysis applied to sorted populations revealed that the TCRαβdim population only disclosed clonal TCR Vβ5, TCR Vβ15, and TCR Vβ23. In contrast, the TCRαβbright population had a profile similar to that of whole PBMCs, including clonal TCR Vβ5, Vβ23, and Vβ15, suggesting that malignant and nonmalignant T-cell clones were present in the TCRαβbright and TCRαβdim subsets. (Bi) Two-color flow cytometry revealed heterogeneity for CD158k expression within the malignant TCR Vβ17 population in patient 1. A proportion of Vβ17+ cells did not express CD158k. A minor Vβ17dim subpopulation could be recognized within the TCR Vβ17+ CD158k+ population (arrowhead). (Bii) Through RT-PCR, CD158k mRNA was detected at significant levels in the TCR Vβ17+ CD158k+ population; negative results were obtained in the TCR Vβ17+ CD158k– population.

Intraclonal heterogeneity for CD158k and TCR Vβ expression in patients 1 and 13 and cell sorting analysis. (Ai) Patient 13 showed 2 distinct TCRαβdim and TCRαβbright circulating T-cell populations. Two-color flow cytometry showed that CD158k+ cells were present within both T-cell populations. (Aii) GeneScan Analysis applied to sorted populations revealed that the TCRαβdim population only disclosed clonal TCR Vβ5, TCR Vβ15, and TCR Vβ23. In contrast, the TCRαβbright population had a profile similar to that of whole PBMCs, including clonal TCR Vβ5, Vβ23, and Vβ15, suggesting that malignant and nonmalignant T-cell clones were present in the TCRαβbright and TCRαβdim subsets. (Bi) Two-color flow cytometry revealed heterogeneity for CD158k expression within the malignant TCR Vβ17 population in patient 1. A proportion of Vβ17+ cells did not express CD158k. A minor Vβ17dim subpopulation could be recognized within the TCR Vβ17+ CD158k+ population (arrowhead). (Bii) Through RT-PCR, CD158k mRNA was detected at significant levels in the TCR Vβ17+ CD158k+ population; negative results were obtained in the TCR Vβ17+ CD158k population.

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