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Contact information

Dr. rer. nat. Markus Chmielewski

Laboratory Tumorgenetics and Immunology

CMMC - Center for Molecular Medicine Cologne

University of Cologne

Robert-Koch-Straße 21

50931 Cologne

 

CV

Academic education

2003 - 2007   Doctoral Studies at the Clinic I of Internal Medicine, University Hospital Cologne, Laboratory of Tumor Genetics and Immunology (Supervisor: Prof. H. Abken und Prof. T. Langer)
1997 - 2003 Studies in Biology at the University of Cologne, external Diploma Thesis at the Clinic I of Internal Medicine, University Hospital Cologne, Laboratory of Tumor Genetics and Immunology (Supervisor: Prof. H. Abken und Prof. T. Langer)

Scientific degrees

05/2020 Priv.-Dozent (habilitation in Molecular Medicine)
06/2007 PhD (Dr.rer.nat.)    
09/2003 Diploma (Biology)

Scientific career

2020 – present Principal Investigator at the University Hospital Cologne (director Prof. M. Hallek), CMMC, AG Chmielewski
2019 - 2020   Research associate at the University Hospital Cologne (director Prof. M. Hallek), Laboratory of Tumor Genetics and Immunology (Dr. Andreas Hombach) 
2015 - 2018  Guest Scientist at the Max Planck Institute for Metabolism Research (Prof. J. Brüning)
2007 - 2018 Postdoctoral research associate at the University Hospital Cologne (director Prof. M. Hallek), Laboratory of Tumor Genetics and Immunology (Prof. H. Abken)

Publications

  • An anti-CD19/CTLA-4 switch improves efficacy and selectivity of CAR T cells targeting CD80/86-upregulated DLBCL

    himeric antigen receptor T cell (CAR T) therapy is a potent treatment for relapsed/refractory (r/r) B cell lymphomas but provides lasting remissions in only ∼40% of patients and is associated with serious adverse events. We identify an upregulation of CD80 and/or CD86 in tumor tissue of (r/r)…

  • Distinct Genetically Determined Origins of Myd88/BCL2-Driven Aggressive Lymphoma Rationalize Targeted Therapeutic Intervention Strategies

    Genomic profiling revealed the identity of at least 5 subtypes of diffuse large B-cell lymphoma (DLBCL), including the MCD/C5 cluster characterized by aberrations in MYD88, BCL2, PRDM1, and/or SPIB. We generated mouse models harboring B cell–specific Prdm1 or Spib aberrations on the background of…

  • Regulatory CAR-T cells in autoimmune diseases: Progress and current challenges

    CAR (Chimeric Antigen Receptor) T-cell therapy has revolutionized the field of oncology in recent years. This innovative shift in cancer treatment also provides the opportunity to improve therapies for many patients suffering from various autoimmune diseases. Recent studies have confirmed the…

  • Sustainable Clinical Development of CAR-T Cells – Switching From Viral Transduction Towards CRISPR-Cas Gene Editing

    T cells modified for expression of Chimeric Antigen Receptors (CARs) were the first gene-modified cell products approved for use in cancer immunotherapy. CAR-T cells engineered with gammaretroviral or lentiviral vectors (RVs/LVs) targeting B-cell lymphomas and leukemias have shown excellent clinical…

  • Noncanonical effector functions of the T-memory-like T-PLL cell are shaped by cooperative TCL1A and TCR signaling

    T-cell prolymphocytic leukemia (T-PLL) is a poor-prognostic neoplasm. Differentiation stage and immune-effector functions of the underlying tumor cell are insufficiently characterized. Constitutive activation of the T-cell leukemia 1A (TCL1A) oncogene distinguishes the (pre)leukemic cell from…