
Haematology research group @UniklinikDUS & @uniklinik_hd working on disease biology, resistance markers and personalized medicine.
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ALT A figure showing the distribution of mutations detected by DNA deep sequencing of flow-sorted hematopoietic-cell fractions at three time points: T1 (leukapheresis material collected for autologous stem-cell transplantation 217 days before CAR T-cells infusion), T2 (leukapheresis material collected for CAR T-cell preparation 140 days before infusion), and T4 (CAR+ T-cell lymphoma sample obtained 60 days after CAR T-cells infusion), according to color-coded categories of variant allele frequency (VAF).

ALT Primary tumor cells are isolated from tissue biopsies, bone marrow or peripheral blood. By treating these cells with clinically available drugs ex vivo, individual vulnerabilities are identified which can be used to treat the patient with the most effective treatment. Many thanks to Emma from @DrawImpacts for this beautiful illustration of the study principle.

ALT Left: Overview of AML sample cohort. The inner circle represents ELN-22 risk groups in total numbers, and the outer circle represents the distribution of in vivo responders and non-responders in ELN-22 risk groups. Right: Viability after ex vivo treatment with daunorubicin and cytarabine separated by ELN-22 risk groups. For details see https://www.nature.com/articles/s43018-023-00645-5/figures/4.
















