A microfluidic bone marrow chip for the safety profiling of biologics in pre-clinical drug development

Abstract Hematologic adverse events are common dose-limiting toxicities in drug development. Classical animal models for preclinical safety assessment of immunotherapies are often limited due to insufficient cross-reactivity with non-human homologous proteins, immune system differences, and ethical...

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Main Authors: Leopold Koenig, Laurent Juglair, Thi Phuong Tao, Susanne Fischer, Inga Clausen, Sabine Imhof-Jung, Niels Janssen, Robert Mader, Daniel Marbach, Jens Niewoehner, Annika Winter, Desirée Schubert
Format: Article
Language:English
Published: Nature Portfolio 2025-05-01
Series:Communications Biology
Online Access:https://doi.org/10.1038/s42003-025-08137-1
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