Dr. Erica R. Vander Mause
Head of LIT / DRFZ Joint RG | Experimental Cell Therapy
The Leibniz Institute for Immunotherapy (LIT) and the German Rheumatology Research Center (DRFZ), a Leibniz Institute, have initiated the independent joint Experimental Cell Therapy Research Group. This venture combines the LIT’s expertise in engineered immune cell therapy with the DRFZ’s expertise in immune-mediated inflammatory diseases. Dr. Erica R. Vander Mause will lead the joint group Experimental Cell Therapy.
Dr. Vander Mause has extensive experience in gene and cell therapy, spanning over ten years across both academic and industrial environments. In the academic context, she developed single chain variable fragment (scFv) binding domains and optimized their affinity to selectively preserve cells with lower antigen density, without diminishing their cytotoxicity against cells exhibiting higher antigen density. She and her team also characterized how affinity affects the efficacy and persistence of CAR T cells. These findings helped demonstrate that trogocytosis is correlated with binding affinity. After her doctoral work, she spent time in industry R&D roles, translating cutting-edge discoveries in synthetic biology and precision genome editing techniques to deliver advanced CAR T cell therapies to the patients who need them.
Dr. Vander Mause’s new lab will leverage her combined academic and industry expertise to develop translatable precision CAR T cell therapies for rheumatic and autoimmune diseases. Her team will harness high-quality, comprehensive multi-omics clinical data, generated by partners at the DRFZ and Charité, to identify pathogenic cell populations. Following identification, she will employ advanced methods in protein design and genetic engineering to develop, characterize, and clinically translate logic-gated CAR T cells that selectively target the pathogenic cells.
Here is a selection of the most important publications from the last few years:
- Vander Mause, E. R., Baker, J. M., Dietze, K. A., Radhakrishnan, S. V., Iraguha, T., Omili, D., Davis, P., Chidester, S. L., Modzelewska, K., Panse, J., Marvin, J. E., Olson, M. L., Steinbach, M., Ng, D. P., Lim, C. S., Atanackovic, D., & Luetkens, T. (2023). Systematic single amino acid affinity tuning of CD229 CAR T cells retains efficacy against multiple myeloma and eliminates on-target off-tumor toxicity. Science Translational Medicine, 15(705). DOI: 10.1126/scitranslmed.add7900. PMID: 37467316
- Vander Mause, E. R., Atanackovic, D., Lim, C. S., & Luetkens, T. (2022). Roadmap to affinity-tuned antibodies for enhanced chimeric antigen receptor T cell function and selectivity. Trends in Biotechnology, 40(7), 875–890. DOI: 10.1016/j.tibtech.2021.12.009. PMID: 35078657
- Olson, M. L., Vander Mause, E. R., Radhakrishnan, S. V., Brody, J. D., Rapoport, A. P., Welm, A. L., Atanackovic, D., & Luetkens, T. (2022). Low-affinity CAR T cells exhibit reduced trogocytosis, preventing rapid antigen loss, and increasing CAR T cell expansion. Leukemia 2022 36:7, 36(7), 1943–1946. DOI: 10.1038/s41375-022-01585-2. PMID: 35490197. PMCID: PMC9252916.
- Partin, A. C., Bruno, R., Shafaattalab, S., Vander Mause, E. R., Winters, A., Daris, M., Gahrs, C., Jette, C. A., DiAndreth, B., Sandberg, M. L., Hamburger, A. E., Kamb, A., & Riley, T. P. (2024). Geometric parameters that affect the behavior of logic-gated CAR T cells. Frontiers in Immunology, 15, 1304765. DOI: 10.3389/fimmu.2024.1304765. PMID: 38343543. PMCID: PMC10853413.
- Lu, P., Vander Mause, E. R, Redd Bowman, K. E., Brown, S. M., Ahne, L., & Lim, C. S. (2019). Mitochondrially targeted p53 or DBD subdomain is superior to wild type p53 in ovarian cancer cells even with strong dominant negative mutant p53. Journal of Ovarian Research, 12(1), 45-. DOI: 10.1186/s13048-019-0516-2. PMID: 31092272. PMCID: PMC6521536.
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Dr. Erica Vander Mause, PhD
Email: Erica.vander-mause@LIT.eu
Email: Erica.vander_mause@DRFZ.de