Human lung model

New Collaboration to Advance Drug Discovery for Pulmonary Fibrosis

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Helmholtz Munich and Boehringer Ingelheim have started a research collaboration to identify new avenues for the treatment of idiopathic pulmonary fibrosis that could improve outcomes in people living with this severe and progressive lung disease. Supported by €1.1 million in funding from Boehringer Ingelheim, the project will apply and further develop single-cell genomics techniques and AI models to analyze drug effects on cultured human lung tissue outside the body.

Combining Experimental and Computational Expertise

Idiopathic pulmonary fibrosis, short IPF, leads to scarring of lung tissue, resulting in a loss in lung function that affects patients’ ability to perform daily activities and can even be life-threatening. While current antifibrotic treatments can slow disease progression, there is a high remaining patient need with no treatments capable of stopping or reversing the disease available to date. This collaboration aims to help close this gap by developing a more physiologically relevant platform for drug discovery, using human lung tissue combined with single-cell transcriptomic analysis and AI models.

At Helmholtz Munich, two research groups are leading the collaboration: the Research Unit for Precision Regenerative Medicine headed by lung expert Prof. Herbert Schiller, and the Institute for Computational Biology, led by biomedical AI specialist Prof. Fabian Theis.

The Schiller Lab has developed advanced methods to analyze drug effects at single-cell resolution in precision-cut human lung slices (hPCLS). This approach will now support pre-clinical testing of new anti-fibrotic candidates. “By working directly with human lung tissue and integrating advanced computational models, we hope to gain a detailed understanding of the cellular circuits driving fibrosis and identify novel ways to target them,” says Schiller.

Meanwhile, the Theis Lab contributes its expertise in machine learning and biomedical AI. The team develops models that analyze and predict the effects of drug candidates at single-cell resolution. “This collaboration allows us to combine experimental biology and data science to better predict how potential drugs, and their combinations might behave in complex human tissues,” Theis explains.

Boehringer Ingelheim has leading expertise in the research, development and provision of medicines for fibrotic lung diseases such as IPF, with one treatment launched and a next generation treatment currently submitted for approval. Besides contributing funding, the company provides a selection of compounds from its pipeline for testing. “We are excited to work with the scientists at Helmholtz Munich to explore novel technologies in our quest to develop future treatment options to further improve patient outcomes in IPF,” says Matthew Thomas, Head of Immunology & Respiratory Research, Germany at Boehringer Ingelheim.

Schiller_Herbert_Transparent_EHC
Prof. Dr. Herbert Schiller

Director Research Unit Precision Regenerative Medicine

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Fabian Theis
Prof. Dr. Dr. Fabian Theis

Director of Computational Health Center, Director of Institute for Computational Biology

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