Nature Communications (Nov 2024)
Multiple myeloma long-term survivors exhibit sustained immune alterations decades after first-line therapy
- Raphael Lutz,
- Florian Grünschläger,
- Malte Simon,
- Mohamed H. S. Awwad,
- Marcus Bauer,
- Schayan Yousefian,
- Niklas Beumer,
- Lea Jopp-Saile,
- Anastasia Sedlmeier,
- Llorenç Solé-Boldo,
- Bogdan Avanesyan,
- Dominik Vonficht,
- Patrick Stelmach,
- Georg Steinbuss,
- Tobias Boch,
- Simon Steiger,
- Marc-Andrea Baertsch,
- Nina Prokoph,
- Karsten Rippe,
- Brian G. M. Durie,
- Claudia Wickenhauser,
- Andreas Trumpp,
- Carsten Müller-Tidow,
- Daniel Hübschmann,
- Niels Weinhold,
- Marc S. Raab,
- Benedikt Brors,
- Hartmut Goldschmidt,
- Charles D. Imbusch,
- Michael Hundemer,
- Simon Haas
Affiliations
- Raphael Lutz
- Department of Medicine V, Hematology, Oncology and Rheumatology, Heidelberg University Hospital
- Florian Grünschläger
- Heidelberg Institute for Stem Cell Technology and Experimental Medicine (HI-STEM gGmbH)
- Malte Simon
- Faculty of Biosciences, Heidelberg University
- Mohamed H. S. Awwad
- Department of Medicine V, Hematology, Oncology and Rheumatology, Heidelberg University Hospital
- Marcus Bauer
- Institute of Pathology, University Hospital Halle, Martin Luther University Halle-
- Schayan Yousefian
- Berlin Institute of Health (BIH) at Charité Universitätsmedizin
- Niklas Beumer
- Faculty of Biosciences, Heidelberg University
- Lea Jopp-Saile
- Heidelberg Institute for Stem Cell Technology and Experimental Medicine (HI-STEM gGmbH)
- Anastasia Sedlmeier
- Computational Oncology, Molecular Precision Oncology Program, National Center for Tumor Diseases (NCT) Heidelberg and German Cancer Research Center (DKFZ)
- Llorenç Solé-Boldo
- Berlin Institute of Health (BIH) at Charité Universitätsmedizin
- Bogdan Avanesyan
- Berlin Institute of Health (BIH) at Charité Universitätsmedizin
- Dominik Vonficht
- Heidelberg Institute for Stem Cell Technology and Experimental Medicine (HI-STEM gGmbH)
- Patrick Stelmach
- Heidelberg Institute for Stem Cell Technology and Experimental Medicine (HI-STEM gGmbH)
- Georg Steinbuss
- Department of Medicine V, Hematology, Oncology and Rheumatology, Heidelberg University Hospital
- Tobias Boch
- Heidelberg Institute for Stem Cell Technology and Experimental Medicine (HI-STEM gGmbH)
- Simon Steiger
- Division of Chromatin Networks, German Cancer Research Center (DKFZ) and BioQuant
- Marc-Andrea Baertsch
- Department of Medicine V, Hematology, Oncology and Rheumatology, Heidelberg University Hospital
- Nina Prokoph
- Department of Medicine V, Hematology, Oncology and Rheumatology, Heidelberg University Hospital
- Karsten Rippe
- Division of Chromatin Networks, German Cancer Research Center (DKFZ) and BioQuant
- Brian G. M. Durie
- Cedars-Sinai Medical Center
- Claudia Wickenhauser
- Institute of Pathology, University Hospital Halle, Martin Luther University Halle-
- Andreas Trumpp
- Heidelberg Institute for Stem Cell Technology and Experimental Medicine (HI-STEM gGmbH)
- Carsten Müller-Tidow
- Department of Medicine V, Hematology, Oncology and Rheumatology, Heidelberg University Hospital
- Daniel Hübschmann
- Heidelberg Institute for Stem Cell Technology and Experimental Medicine (HI-STEM gGmbH)
- Niels Weinhold
- Department of Medicine V, Hematology, Oncology and Rheumatology, Heidelberg University Hospital
- Marc S. Raab
- Department of Medicine V, Hematology, Oncology and Rheumatology, Heidelberg University Hospital
- Benedikt Brors
- Division of Applied Bioinformatics, German Cancer Research Center (DKFZ)
- Hartmut Goldschmidt
- Department of Medicine V, Hematology, Oncology and Rheumatology, GMMG Studygroup, Heidelberg University Hospital
- Charles D. Imbusch
- Division of Applied Bioinformatics, German Cancer Research Center (DKFZ)
- Michael Hundemer
- Department of Medicine V, Hematology, Oncology and Rheumatology, Heidelberg University Hospital
- Simon Haas
- Heidelberg Institute for Stem Cell Technology and Experimental Medicine (HI-STEM gGmbH)
- DOI
- https://doi.org/10.1038/s41467-024-54543-0
- Journal volume & issue
-
Vol. 15,
no. 1
pp. 1 – 18
Abstract
Abstract The long-term consequences of cancer and its therapy on the patients’ immune system years after cancer-free survival remain poorly understood. Here, we present an in-depth characterization of the bone marrow immune ecosystem of multiple myeloma long-term survivors, from initial diagnosis up to 17 years following a single therapy line and cancer-free survival. Using comparative single-cell analyses combined with molecular, genomic, and functional approaches, we demonstrate that multiple myeloma long-term survivors exhibit pronounced alterations in their bone marrow microenvironment associated with impaired immunity. These immunological alterations were frequently linked to an inflammatory immune circuit fueled by the long-term persistence or resurgence of residual myeloma cells. Notably, even in the complete absence of any detectable residual disease for decades, sustained changes in the immune system were observed, suggesting an irreversible ‘immunological scarring’ caused by the initial exposure to the cancer and therapy. Collectively, our study provides key insights into the molecular and cellular bone marrow ecosystem of long-term survivors of multiple myeloma, revealing both reversible and irreversible alterations in the immune compartment.