Figure 4.
Figure 4. Xenotransplantation of MDS cells in NSG mice. (A-B) Immunophenotypic profiling of human cells in NSG mice. Shown are percentages of hCD45+, myeloid (CD14+ or CD15+), and B lymphoid (CD19+) cells in the hCD45+ cell fraction, at 5 to 15 weeks posttransplantation. (C-G) Genotype of sorted MDS CD14+CD15+, CD19+, or CD34+ populations after xenografting. Shown are VAFs and the 95% CIs of each mutation in BM MNCs, PDX CD14+CD15+, PDX CD19+, and PDX CD34+. In UPNs 2, 10, and 12, mutations were screened by NGS. For UPN 8, mutations in PDX CD14+CD15+ and CD19+ populations were detected by Sanger sequencing on amplified whole genome DNA. (D) For UPN 2, hypotheses regarding the contribution of CD34+-mutated clones to their myeloid CD14+CD15+ (My) and lymphoid CD19+ (Ly) progenies are schematically depicted. Each mutation is represented by its initial. A color spectrum is used for the different intervals of variant allele frequencies.

Xenotransplantation of MDS cells in NSG mice. (A-B) Immunophenotypic profiling of human cells in NSG mice. Shown are percentages of hCD45+, myeloid (CD14+ or CD15+), and B lymphoid (CD19+) cells in the hCD45+ cell fraction, at 5 to 15 weeks posttransplantation. (C-G) Genotype of sorted MDS CD14+CD15+, CD19+, or CD34+ populations after xenografting. Shown are VAFs and the 95% CIs of each mutation in BM MNCs, PDX CD14+CD15+, PDX CD19+, and PDX CD34+. In UPNs 2, 10, and 12, mutations were screened by NGS. For UPN 8, mutations in PDX CD14+CD15+ and CD19+ populations were detected by Sanger sequencing on amplified whole genome DNA. (D) For UPN 2, hypotheses regarding the contribution of CD34+-mutated clones to their myeloid CD14+CD15+ (My) and lymphoid CD19+ (Ly) progenies are schematically depicted. Each mutation is represented by its initial. A color spectrum is used for the different intervals of variant allele frequencies.

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