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Detail

Dietmar Herndler-Brandstetter
Ap.Prof. Mag.pharm. Dietmar Herndler-Brandstetter, PhDGroup Leader

Center for Cancer Research, Comprehensive Cancer Center
Position: Associate Professor

ORCID: 0000-0003-0987-0208
T +43 1 40160 - 57577
dietmar.herndler-brandstetter@meduniwien.ac.at

Further Information

Keywords

Colorectal Neoplasms; Immune System; Immunotherapy; Tumor Microenvironment

Research interests

  • Humanized mouse models for translational cancer research and immunotherapy
  • Stromal regulation of immune cell development and anti-tumor immunity

Techniques, methods & infrastructure

  • Next-generation humanized mouse models (MISTRG-6)
  • Colorectal cancer patient-derived tumor xenograft (CRC-PDX) models
  • Cancer immunotherapies
  • Reporter and conditional knockout mouse models
  • Spectral flow cytometry (Cytek Aurora)
  • Multiplex immunohistochemistry

Grants

Selected publications

  1. Stecher, C. et al. (2025) ‘Heterogeneity of IL-15-expressing mesenchymal stromal cells controls natural killer cell development and immune cell homeostasis’, Nature Communications, 16(1). Available at: https://doi.org/10.1038/s41467-025-61231-0.
  2. Herndler-Brandstetter, D. et al. (2018) ‘KLRG1+ Effector CD8+ T Cells Lose KLRG1, Differentiate into All Memory T Cell Lineages, and Convey Enhanced Protective Immunity’, Immunity, 48(4), pp. 716-729.e8. Available at: https://doi.org/10.1016/j.immuni.2018.03.015.
  3. Ring, N.G. et al. (2017) ‘Anti-SIRPα antibody immunotherapy enhances neutrophil and macrophage antitumor activity’, Proceedings of the National Academy of Sciences, 114(49). Available at: https://doi.org/10.1073/pnas.1710877114.
  4. Chen, A., Neuwirth, I. and Herndler-Brandstetter, D. (2023) ‘Modeling the Tumor Microenvironment and Cancer Immunotherapy in Next-Generation Humanized Mice’, Cancers, 15(11), p. 2989. Available at: http://dx.doi.org/10.3390/cancers15112989.
  5. Chen, A. et al. (2025) ‘Comparison of NSG-Quad and MISTRG-6 humanized mice for modeling circulating and tumor-infiltrating human myeloid cells’, Molecular Therapy Methods & Clinical Development, 33(2), p. 101487. Available at: https://doi.org/10.1016/j.omtm.2025.101487.