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Journal of Blood Medicine Volume 12, 2021 - Issue

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Review

Complement in Sickle Cell Disease: Are We Ready for Prime Time?

Christos Varelas1 Hematology Department – BMT Unit, G. Papanicolaou Hospital, Thessaloniki, Greece

Athina Tampaki2 Adults Thalassemia Unit, 2nd Department of Internal Medicine, Hippokration Hospital, Thessaloniki, Greece

https://orcid.org/0000-0002-4690-2865

Ioanna Sakellari1 Hematology Department – BMT Unit, G. Papanicolaou Hospital, Thessaloniki, Greece

Αchilles Anagnostopoulos1 Hematology Department – BMT Unit, G. Papanicolaou Hospital, Thessaloniki, Greece

Eleni Gavriilaki1 Hematology Department – BMT Unit, G. Papanicolaou Hospital, Thessaloniki, GreeceCorrespondence[email protected]

Efthymia Vlachaki2 Adults Thalassemia Unit, 2nd Department of Internal Medicine, Hippokration Hospital, Thessaloniki, Greece

https://orcid.org/0000-0002-2043-9630

Pages 177-187 | Published online: 23 Mar 2021

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Citations (3)

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Marta Ferraresi, Daniele Lello Panzieri, Simona Leoni, Maria Domenica Cappellini, Antonis Kattamis & Irene Motta. (2023) Therapeutic perspective for children and young adults living with thalassemia and sickle cell disease. European Journal of Pediatrics 182:6, pages 2509-2519.
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Yvette C. Tanhehco, Ghazala Nathu & Ljiljana V. Vasovic. (2022) Development of curative therapies for sickle cell disease. Frontiers in Medicine 9.
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John D. Belcher, Julia Nguyen, Chunsheng Chen, Fuad Abdulla, Ruan Conglin, Zalaya K. Ivy, Jason Cummings, Thomas Dudler & Gregory M. Vercellotti. (2022) MASP-2 and MASP-3 inhibitors block complement activation, inflammation, and microvascular stasis in a murine model of vaso-occlusion in sickle cell disease. Translational Research 249, pages 1-12.
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