Research Training Group Tumor-Targeted Drug Delivery

DFG Research Training Group - Tumor-Targeted Drug Delivery

Motivation and problem definition

The overarching goal of the Research Training Group (RTG) entitled "Tumor-Targeted Drug Delivery" [2(TD)] is to address current challenges in the development of drug delivery for tumor diseases and to explore therapeutic and theranosetic scenarios that lead to improved patient outcomes and offer a clear perspective for clinical translation.

While the majority of drug delivery research consortia in Germany and Europe primarily focus on novel materials for nanomedicine, 2(TD) will concentrate on medical needs and clinical applications, aiming to systematically identify and overcome pitfalls in the translation of tumor-targeted drug delivery concepts. To this end, the 2(TD) consortium will generate knowledge and foster collaboration at the interfaces of the key fields of tumor biology, chemical engineering, and clinical medicine.

While the majority of drug delivery research consortia in Germany and Europe primarily focus on novel materials for nanomedicine, 2(TD) will concentrate on medical needs and clinical applications, aiming to systematically identify and overcome obstacles in the translation of tumor-targeted drug delivery concepts. The Research Training Group 2(TD) aims to generate fundamental knowledge and translational strategies for improving the treatment of cancer patients with DDS-based targeted drug therapies. The interdisciplinary and international nature of 2(TD) will enhance the quality and visibility of our research and improve the training and career prospects of our doctoral students.

Project goals and solution approach

Complex biopharmaceuticals such as antibody-drug conjugates (ADCs) and recombinant immunotoxins (RITs) enable the targeted delivery of toxic protein drugs to cancer cells (as drug-disrupting systems). While ADCs incur high production costs because the monoclonal antibody and the toxic drug must be produced separately and then chemically coupled, RITs can be manufactured as a single fusion protein, which could reduce costs.

Plants have proven to be the most efficient environment for their production, as RITs can be targeted to different compartments where they do not interfere with host metabolism. Plant cell packs (PCPs), derived from plant suspension cells, provide a high-throughput screening platform for the production of recombinant protein candidates in plants. Within the framework of the GRK 2(TD), Fraunhofer applies this know-how in antibody engineering and fusion protein design for DDS development and provides small quantities of the target protein (mg range) to the other partners of the GRK.

Project profile

Project title

GRK 2375: Tumor-Targeted Drug Delivery         

Duration seit 2018     
Promotion

Deutsche Forschungsgemeinschaft DFG

Partner
  • Rheinisch-Westfälische Technische Hochschule Aachen (Coordination)
  • several institutes of the University Hospital Aachen
  • DWI - Leibniz Institute for Interactive  Materials e.V.
  • Fraunhofer Institute for Molecular Biology and Applied Ecology IME
Speaker Professor Dr. Fabian Kiessling
Goals
  • Transdisciplinary research and translation of drug delivery systems into clinical application
  • Qualification of young scientists in the field of drug delivery systems

Publications from the graduate school with the participation of Fraunhofer IME

Plant based human ferritin heavy chain as a nanocarrier for tumor-targeted drug delivery and bioimaging

Plant-made immunotoxin building blocks: A roadmap for producing therapeutic antibody-toxin fusions

Interleukin-6 and 8 expression in plant cell packs for medical application in advanced therapy medicinal products

Spherical nanoparticles in packed-bed chromatography columns

Recombinant immunotoxins expressed in plants and plant cells for the treatment of monocytic leukemia

The use of predictive models to develop chromatography-based purification processes

Activated Cross-linked Agarose for the Rapid Development of Affinity Chromatography Resins - Antibody Capture

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Stefan Schillberg

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Prof. Dr. Stefan Schillberg

Principal Investigator

Fraunhofer Institute for Molecular Biology and Applied Ecology IME
Forckenbeckstr. 6
52074 Aachen

Phone +49 241 6085-202

Henrik Nausch

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Dr. Henrik Nausch

Head of Department »Model-based Product and Bioprocess Engineering«

Fraunhofer Institute for Molecular Biology and Applied Ecology IME
Forckenbeckstr. 6
52074 Aachen

Phone +49 241 6085-184

Jannik Lutz

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Jannik Lutz

Fraunhofer Institute for Molecular Biology and Applied Ecology IME
Forckenbeckstr. 6
52074 Aachen

Phone +49 241 6085-175

Monique Schulze

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Monique Schulze

Fraunhofer Institute for Molecular Biology and Applied Ecology IME
Forckenbeckstr. 6
52074 Aachen

Phone +49 241 6085-206