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Hemoglobin
international journal for hemoglobin research
Volume 42, 2018 - Issue 5-6
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Short Communication

Successful Outcome of Hyperhemolysis in Sickle Cell Disease following Multiple Lines of Treatment: The Role of Complement Inhibition

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Pages 339-341 | Received 22 Sep 2018, Accepted 20 Oct 2018, Published online: 09 Jan 2019

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Read on this site (2)

Christos Varelas, Athina Tampaki, Ioanna Sakellari, Αchilles Anagnostopoulos, Eleni Gavriilaki & Efthymia Vlachaki. (2021) Complement in Sickle Cell Disease: Are We Ready for Prime Time?. Journal of Blood Medicine 12, pages 177-187.
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Sawsan A Omer, Jafar S Alaesh & Kefah B Algadeeb. (2020) Delayed Hemolytic Transfusion Reaction in a Patient with Sickle Cell Disease: Case Report. International Medical Case Reports Journal 13, pages 307-311.
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Articles from other publishers (17)

France Pirenne & Corinne Pondarré. (2023) Alloimmunization and hyperhemolysis in sickle cell disease. Hematology 2023:1, pages 653-659.
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Christos Varelas & Eleni Gavriilaki. (2023) Sickle Cell Disease: Current Understanding and Future Options. Journal of Clinical Medicine 12:18, pages 5943.
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Anna Duval & Véronique Frémeaux‐Bacchi. (2023) Complement biology for hematologists. American Journal of Hematology 98:S4.
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Mark T. Friedman, Kamille A. West, Peyman Bizargity, Kyle Annen, H. Deniz Gur & Timothy HilbertMark T. Friedman, Kamille A. West, Peyman Bizargity, Kyle Annen, H. Deniz Gur & Timothy Hilbert. 2023. Immunohematology, Transfusion Medicine, Hemostasis, and Cellular Therapy. Immunohematology, Transfusion Medicine, Hemostasis, and Cellular Therapy 323 329 .
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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Eleni Gavriilaki, Régis Peffault de Latour & Antonio Maria Risitano. (2022) Advancing therapeutic complement inhibition in hematologic diseases: PNH and beyond. Blood 139:25, pages 3571-3582.
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Christos Varelas, Eleni Gavriilaki, Ioanna Sakellari, Philippos Klonizakis, Evaggelia-Evdoxia Koravou, Ioanna Christodoulou, Ioulia Mavrikou, Andreas Kourelis, Fani Chatzopoulou, Dimitrios Chatzidimitriou, Tasoula Touloumenidou, Apostolia Papalexandri, Achilles Anagnostopoulos & Efthimia Vlachaki. (2022) Immune Response of Adult Sickle Cell Disease Patients after COVID-19 Vaccination: The Experience of a Greek Center. Journal of Clinical Medicine 11:4, pages 937.
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Rim Abdallah, Herleen Rai & Sandhya R. Panch. (2021) Transfusion Reactions and Adverse Events. Clinics in Laboratory Medicine 41:4, pages 669-696.
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Richard C. Zanetti, Lauren M. Vasta, Kristen Romanelli & Thomas C. Newton. (2021) Management of Hyperhemolysis in β-thalassemia With Multiple Immunosuppressives, Including Complement Blockade. Journal of Pediatric Hematology/Oncology 43:8, pages e1145-e1147.
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Athina Tampaki, Eleni Gavriilaki, Christos Varelas, Achilles Anagnostopoulos & Efthymia Vlachaki. (2021) Complement in sickle cell disease and targeted therapy: I know one thing, that I know nothing. Blood Reviews 48, pages 100805.
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Grace E. Linder & Stella T. Chou. (2021) Red cell transfusion and alloimmunization in sickle cell disease. Haematologica 106:7, pages 1805-1815.
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Yuanjun Wu, Yanli Ji, Bingmei Dai, Faliang Guo, Yong Wu, Ziyi He, Chunyan Mo, Shujie Wu & Yingming Hu. (2020) A case of hyperhaemolysis syndrome in a pregnant Chinese woman with β‐thalassemia during perinatal transfusion. Transfusion Medicine 31:1, pages 24-29.
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Melissa Azul, Surbhi Shah, Sarah Williams, Gregory M. Vercellotti & Alexander A. Boucher. (2021) Evidence for complement-mediated bone marrow necrosis in a young adult with sickle cell disease. Blood Cells, Molecules, and Diseases 86, pages 102508.
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Lakshman Vasanthamohan, Sheryl Choo, Tonisha Marshall, Yahui Tammy Symons, Doreen Matsui, Genevieve Eastabrook & Ziad Solh. (2020) Peripartum hyperhemolysis prophylaxis and management in sickle cell disease: A case report and narrative review. Transfusion 60:10, pages 2448-2455.
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Aline Floch, Alexandre Morel, Fabian Zanchetta-Balint, Catherine Cordonnier-Jourdin, Slimane Allali, Maximilien Grall, Ghislaine Ithier, Benjamin Carpentier, Sadaf Pakdaman, Jean-Claude Merle, Radjiv Goulabchand, Tackwa Khalifeh, Ana Berceanu, Cécile Helmer, Christelle Chantalat-Auger, Véronique Frémeaux-Bacchi, Marc Michel, Mariane de Montalembert, Armand Mekontso-Dessap, France Pirenne, Anoosha Habibi & Pablo Bartolucci. (2020) Anti-C5 antibody treatment for delayed hemolytic transfusion reactions in sickle cell disease. Haematologica 105:11, pages 2694-2697.
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France Pirenne. (2019) The cause and pathogenesis of hemolytic transfusion reactions in sickle-cell disease. Current Opinion in Hematology 26:6, pages 488-494.
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Christopher J Patriquin & Kevin H.M. Kuo. (2019) Eculizumab and Beyond: The Past, Present, and Future of Complement Therapeutics. Transfusion Medicine Reviews 33:4, pages 256-265.
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