Fig. 1: CD79a has independent prognostic relevance for CNS-involvement and CNS-relapse in BCP-ALL patients. | Communications Biology

Fig. 1: CD79a has independent prognostic relevance for CNS-involvement and CNS-relapse in BCP-ALL patients.

From: CD79a promotes CNS-infiltration and leukemia engraftment in pediatric B-cell precursor acute lymphoblastic leukemia

Fig. 1: CD79a has independent prognostic relevance for CNS-involvement and CNS-relapse in BCP-ALL patients.The alternative text for this image may have been generated using AI.

ac CD79a mRNA levels and further genes (all normalized to mRNA levels in the 697 cell line) were measured in diagnostic BM samples in a selected cohort of 100 pediatric BCP-ALL patients of mixed cytogenetics which contained 28 CNS-positive patients matched to 72 CNS-negative patients of corresponding sex and age5. a, b Bivariate correlation analysis between CD79a expression and a ZAP70 and b Interleukin-7-receptor (IL7R) were performed, Spearman correlation (two-tailed, respective 95% confidence interval (CI) [0.08789, 0.4605] and [0.2174, 0.5616]). c Univariate and multivariate logistic regression analysis for risk of initial CNS-involvement, controlled for age and white blood cell (WBC) count at diagnosis as well as TEL-AML and BCR-ABL positivity. *Based on expression as measured by RT-PCR of patient material at initial diagnosis. Multivariate OR controlled for age and WBC count at diagnosis as well as TEL-AML and BCR-ABL positivity. §Reference category. Definitions of patient CNS status in Supplementary Material d Kaplan–Meier survival curve showing reduced isolated CNS-relapse-free survival in children with upregulated CD79a gene expression in diagnostic BM/peripheral blood (upregulation is defined as z-score for gene expression ≥1.2 which is equivalent to the 11.5% top CD79a-expressing patients; TARGET phase 1 dataset). e E2A-PBX1 + BCP-ALL blasts from seven different patient-derived xenograft (PDX) samples were injected into NSG mice ALL cells were recovered from spleen (SP) and CNS and subjected to quantitative real-time PCR (qPCR). QPCR shows the upregulation of CD79a at the transcription level in PDX cells recovered from the CNS relative to cells isolated from Sp, Mann–Whitney-U test, two-tailed, graphs show mean with standard error of n = 7 independent samples. f An upregulation of CD79a was also observed in CNS-BCP-ALL cells compared to SP-BCP-ALL cells in NSG-mice injected with bone marrow cells from BCP-ALL patients of different cytogenetic backgrounds (n = 5 independent patient samples) or CNS-tropic REH cells (TEL-AML1) as determined via qPCR. Relative quantification of CD79a mRNA levels normalized to 697 cells are shown for individual patients, P Patient, AU Arbitrary units. *P < 0.05, **P ≤ 0.01, ***P ≤ 0.001.

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