Communications Biology (Dec 2023)
Impaired FADD/BID signaling mediates cross-resistance to immunotherapy in Multiple Myeloma
- Umair Munawar,
- Xiang Zhou,
- Sabrina Prommersberger,
- Silvia Nerreter,
- Cornelia Vogt,
- Maximilian J. Steinhardt,
- Marietta Truger,
- Julia Mersi,
- Eva Teufel,
- Seungbin Han,
- Larissa Haertle,
- Nicole Banholzer,
- Patrick Eiring,
- Sophia Danhof,
- Miguel Angel Navarro-Aguadero,
- Adrian Fernandez-Martin,
- Alejandra Ortiz-Ruiz,
- Santiago Barrio,
- Miguel Gallardo,
- Antonio Valeri,
- Eva Castellano,
- Peter Raab,
- Maximilian Rudert,
- Claudia Haferlach,
- Markus Sauer,
- Michael Hudecek,
- J. Martinez-Lopez,
- Johannes Waldschmidt,
- Hermann Einsele,
- Leo Rasche,
- K. Martin Kortüm
Affiliations
- Umair Munawar
- Department of Internal Medicine II, University Hospital of Würzburg
- Xiang Zhou
- Department of Internal Medicine II, University Hospital of Würzburg
- Sabrina Prommersberger
- Department of Internal Medicine II, University Hospital of Würzburg
- Silvia Nerreter
- Department of Internal Medicine II, University Hospital of Würzburg
- Cornelia Vogt
- Department of Internal Medicine II, University Hospital of Würzburg
- Maximilian J. Steinhardt
- Department of Internal Medicine II, University Hospital of Würzburg
- Marietta Truger
- MLL Munich Leukemia Laboratory
- Julia Mersi
- Department of Internal Medicine II, University Hospital of Würzburg
- Eva Teufel
- Department of Internal Medicine II, University Hospital of Würzburg
- Seungbin Han
- Department of Internal Medicine II, University Hospital of Würzburg
- Larissa Haertle
- Department of Internal Medicine II, University Hospital of Würzburg
- Nicole Banholzer
- Department of Biotechnology and Biophysics, University of Würzburg
- Patrick Eiring
- Department of Biotechnology and Biophysics, University of Würzburg
- Sophia Danhof
- Department of Internal Medicine II, University Hospital of Würzburg
- Miguel Angel Navarro-Aguadero
- Department of Hematology, Hospital Universitario 12 de Octubre, CNIO, Complutense University Madrid
- Adrian Fernandez-Martin
- Department of Hematology, Hospital Universitario 12 de Octubre, CNIO, Complutense University Madrid
- Alejandra Ortiz-Ruiz
- Department of Hematology, Hospital Universitario 12 de Octubre, CNIO, Complutense University Madrid
- Santiago Barrio
- Department of Hematology, Hospital Universitario 12 de Octubre, CNIO, Complutense University Madrid
- Miguel Gallardo
- Department of Hematology, Hospital Universitario 12 de Octubre, CNIO, Complutense University Madrid
- Antonio Valeri
- Department of Hematology, Hospital Universitario 12 de Octubre, CNIO, Complutense University Madrid
- Eva Castellano
- Department of Hematology, Hospital Universitario 12 de Octubre, CNIO, Complutense University Madrid
- Peter Raab
- Department of Orthopaedic Surgery, König Ludwig Haus, University of Würzburg
- Maximilian Rudert
- Department of Orthopaedic Surgery, König Ludwig Haus, University of Würzburg
- Claudia Haferlach
- MLL Munich Leukemia Laboratory
- Markus Sauer
- Department of Hematology, Hospital Universitario 12 de Octubre, CNIO, Complutense University Madrid
- Michael Hudecek
- Department of Internal Medicine II, University Hospital of Würzburg
- J. Martinez-Lopez
- Department of Biotechnology and Biophysics, University of Würzburg
- Johannes Waldschmidt
- Department of Internal Medicine II, University Hospital of Würzburg
- Hermann Einsele
- Department of Internal Medicine II, University Hospital of Würzburg
- Leo Rasche
- Department of Internal Medicine II, University Hospital of Würzburg
- K. Martin Kortüm
- Department of Internal Medicine II, University Hospital of Würzburg
- DOI
- https://doi.org/10.1038/s42003-023-05683-4
- Journal volume & issue
-
Vol. 6,
no. 1
pp. 1 – 9
Abstract
Abstract The treatment landscape in multiple myeloma (MM) is shifting from genotoxic drugs to immunotherapies. Monoclonal antibodies, immunoconjugates, T-cell engaging antibodies and CART cells have been incorporated into routine treatment algorithms, resulting in improved response rates. Nevertheless, patients continue to relapse and the underlying mechanisms of resistance remain poorly understood. While Impaired death receptor signaling has been reported to mediate resistance to CART in acute lymphoblastic leukemia, this mechanism yet remains to be elucidated in context of novel immunotherapies for MM. Here, we describe impaired death receptor signaling as a novel mechanism of resistance to T-cell mediated immunotherapies in MM. This resistance seems exclusive to novel immunotherapies while sensitivity to conventional anti-tumor therapies being preserved in vitro. As a proof of concept, we present a confirmatory clinical case indicating that the FADD/BID axis is required for meaningful responses to novel immunotherapies thus we report impaired death receptor signaling as a novel resistance mechanism to T-cell mediated immunotherapy in MM.