Colchicine Protects Against Sickle Cell Related Cardiomyopathy: Evidence of the Novel Role of Inflammaging

Sickle cell disease (SCD) is a globally distributed hereditary red cell disorder with still high mortality. Growing evidence indicates that sickle cell related cardiovascular disease contributes to the early death of adults with SCD. Here, we show that humanized SCD mice developed an age-dependent cardiomyopathy characterized by (i) increased circulating Th17 lymphocytes, Th17 heart infiltration associated with increased plasma IL-17; (ii) collagen deposition and activation of both platelet derived growth factor-B (PDGF-B) and transforming growth factor-β1 (TGF-β1) canonical pathways; (iii) overactivation of heart NF-κB associated with up-regulation of NLRP3 and of inflammatory vasculopathy markers. We then used colchicine (CLC) that acts as anti-inflammatory drug with immunomodulatory effects. In humanized SCD mice, we demonstrated the protective role of low-dose CLC treatment against chronic inflammation and preserving myocardial performance. Of note, we found CLC also attenuating sickle cell related lung damage, suggesting a multiorgan effect of CLC in SCD mice. Our data generate the rationale to further explore CLC as new therapeutic tool to treat early stages of sickle cell cardiomyopathy.

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Publication Details

Journal
Antioxidants
Published
2026-07-23
DOI
https://doi.org/10.3390/antiox15080912
Primary Topic
Hemoglobinopathies and Related Disorders
Type
article
Field-Weighted Citation Impact
0.00

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article

Colchicine Protects Against Sickle Cell Related Cardiomyopathy: Evidence of the Novel Role of Inflammaging

Alessandro Mattè, Achille Iolascon, Enrica Federti, Antonio Recchiuti et al.
Antioxidants
Hemoglobinopathies and Related Disorders
article

Colchicine Protects Against Sickle Cell Related Cardiomyopathy: Evidence of the Novel Role of Inflammaging

Alessandro Mattè, Achille Iolascon, Enrica Federti, Antonio Recchiuti, Emanuela Tolosano, Alessandra Ghigo, Immacolata Andolfo, Lucia De Franceschi, Veronica Riccardi, Iana Iatcenko, Manuela Stella, Rebecca Priolo, Jacopo Ceolan, Filippo Mazzi, Elisa Gremese, Richard Pozzetto Huot, Gian Luca Forni, Simone Villaboni
article en

Abstract

Sickle cell disease (SCD) is a globally distributed hereditary red cell disorder with still high mortality. Growing evidence indicates that sickle cell related cardiovascular disease contributes to the early death of adults with SCD. Here, we show that humanized SCD mice developed an age-dependent cardiomyopathy characterized by (i) increased circulating Th17 lymphocytes, Th17 heart infiltration associated with increased plasma IL-17; (ii) collagen deposition and activation of both platelet derived growth factor-B (PDGF-B) and transforming growth factor-β1 (TGF-β1) canonical pathways; (iii) overactivation of heart NF-κB associated with up-regulation of NLRP3 and of inflammatory vasculopathy markers. We then used colchicine (CLC) that acts as anti-inflammatory drug with immunomodulatory effects. In humanized SCD mice, we demonstrated the protective role of low-dose CLC treatment against chronic inflammation and preserving myocardial performance. Of note, we found CLC also attenuating sickle cell related lung damage, suggesting a multiorgan effect of CLC in SCD mice. Our data generate the rationale to further explore CLC as new therapeutic tool to treat early stages of sickle cell cardiomyopathy.

AntioxidantsVol. 15(8)
University of Verona (IT), Humanitas University (IT), Istituto Giannina Gaslini (IT), University of Chieti-Pescara (IT), Azienda Ospedaliera Universitaria Integrata Verona (IT), CEINGE Biotecnologie Avanzate Franco Salvatore (Italy) (IT), IRCCS Humanitas Research Hospital (IT), University of Turin (IT), University of Naples Federico II (IT), University of Genoa (IT)
European Hematology Association
Good health and well-being
Openalex Percentile: Top 9%
Hemoglobinopathies and Related Disorders
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