<scp>CD71</scp><sup>+</sup> erythroid cells promote multiple myeloma progression and impair anti‐bacterial immune response

Multiple myeloma (MM), one of the most frequent haematological malignancies, significantly increases the risk of bacterial infections due to treatment-related side effects, comorbidities and cancer-induced immune deficiencies. Recently, CD71<sup>+</sup> erythroid cells (CECs) have been identified as key immunomodulators in neonates and cancer patients, but their role in MM progression remains unclear. Using a murine MM model, closely resembling human disease, we observed that MM progression is associated with anaemia and an increase in immature CECs, which are characterized by elevated arginase 2 (ARG2) expression. These MM-associated CECs suppress T-cell proliferation, contributing to impaired immune responses. Notably, ARG2 deficiency in mice led to slower MM progression and improved survival. Furthermore, MM-bearing mice exhibited higher susceptibility to Listeria monocytogenes infections, mirroring the increased infection risk in MM patients. Our findings suggest that ARG2-expressing CECs play a critical role in MM-associated immune suppression and infection susceptibility, pointing out ARG2 as a potential therapeutic target to enhance immune function and reduce infection risks in MM patients.

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Publication Details

Journal
British Journal of Haematology
Published
2024-11-20
DOI
https://doi.org/10.1111/bjh.19914
Citations
4
Primary Topic
Immune Cell Function and Interaction
Type
article
Field-Weighted Citation Impact
0.96
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article

CD71+ erythroid cells promote multiple myeloma progression and impair anti‐bacterial immune response

Aleksander Jerzy Owczarek, Olga Gewartowska, Tomasz Skirecki, Zofia Pilch et al.
4 citations
British Journal of Haematology
Immune Cell Function and Interaction
0.96
article

CD71+ erythroid cells promote multiple myeloma progression and impair anti‐bacterial immune response

Aleksander Jerzy Owczarek, Olga Gewartowska, Tomasz Skirecki, Zofia Pilch, Grażyna Hoser, Olga Ciepiela, Michał Węgrzynowicz, Karol Czubak, Milena Małecka‐Giełdowska, Przemysław Juszczyński, Filip Garbicz, Dominika Nowis, Tomasz M. Grzywa, Joanna Barankiewicz, Kamil Bielak, Karolina Sidor-Dzitkowska
article en
4 citations

Abstract

Multiple myeloma (MM), one of the most frequent haematological malignancies, significantly increases the risk of bacterial infections due to treatment-related side effects, comorbidities and cancer-induced immune deficiencies. Recently, CD71<sup>+</sup> erythroid cells (CECs) have been identified as key immunomodulators in neonates and cancer patients, but their role in MM progression remains unclear. Using a murine MM model, closely resembling human disease, we observed that MM progression is associated with anaemia and an increase in immature CECs, which are characterized by elevated arginase 2 (ARG2) expression. These MM-associated CECs suppress T-cell proliferation, contributing to impaired immune responses. Notably, ARG2 deficiency in mice led to slower MM progression and improved survival. Furthermore, MM-bearing mice exhibited higher susceptibility to Listeria monocytogenes infections, mirroring the increased infection risk in MM patients. Our findings suggest that ARG2-expressing CECs play a critical role in MM-associated immune suppression and infection susceptibility, pointing out ARG2 as a potential therapeutic target to enhance immune function and reduce infection risks in MM patients.

British Journal of HaematologyVol. 206(2)
Medical University of Warsaw (PL), Instytut Hematologii i Transfuzjologi (PL), International Institute of Molecular and Cell Biology (PL), Postgraduate School of Molecular Medicine (PL), Polish Academy of Sciences (PL)
Good health and well-being
Openalex Percentile: Top 24%
Immune Cell Function and Interaction
0.96
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