Pure red cell aplasia after major or bidirectional abo incompatible hematopoietic stem cell transplantation: to treat or not to treat, that is the question
Pure red cell aplasia after major or bidirectional abo incompatible hematopoietic stem cell transplantation: to treat or not to treat, that is the question"
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ABSTRACT Pure red cell aplasia (PRCA) is a complication related to major or bidirectional ABO mismatched hematopoietic stem cell transplantation. This disorder is characterized by anemia,
reticulocytopenia, and the absence or virtual absence of erythroid progenitors, other causes such as infections, hemolysis, disease relapse, or drug toxicity having been excluded. Patients
with PRCA may become RBC transfusion dependent for long periods, suffering an important long-term iron overload, alloimmunization, and transfusion reactions. The persistence of recipient
isoagglutinins against donor ABO antigens produced by host residual plasmatic cells has been considered as the immunological cause of the prolonged erythroid aplasia. PRCA behaves in many
cases as a self-limited condition and resolution may occur spontaneously within weeks, months, and even years. Many different therapeutic approaches have been reported for posttransplant
PRCA as plasmapheresis, high doses of erythropoietin, donor lymphocyte infusions, anti-thymocyte globulin, Rituximab and steroids, among others. However, to date there is no standard of care
and the question if patients with PRCA should be treated and at which point remains. The objective of this article is to review the natural evolution of PRCA, and the treatments that have
been used over time focusing on their suitability and efficacy. Access through your institution Buy or subscribe This is a preview of subscription content, access via your institution ACCESS
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institutional subscriptions * Read our FAQs * Contact customer support SIMILAR CONTENT BEING VIEWED BY OTHERS RITUXIMAB ADDED TO CONDITIONING REGIMEN SIGNIFICANTLY IMPROVES ERYTHROID
ENGRAFTMENT IN MAJOR INCOMPATIBLE ABO-GROUP HEMATOPOIETIC STEM CELL TRANSPLANTATION Article Open access 24 February 2024 THE ROLE OF DARATUMUMAB IN COMPLICATIONS POST-ALLOGENEIC
HEMATOPOIETIC STEM CELL TRANSPLANTATION: A SINGLE-CENTER PROSPECTIVE STUDY ON PRCA AND AIHA Article 20 November 2024 SIROLIMUS IS EFFECTIVE FOR REFRACTORY/RELAPSED/INTOLERANT ACQUIRED PURE
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INFORMATION AUTHORS AND AFFILIATIONS * Hospital Universitario y Politécnico La Fe, Valencia, Spain Javier Marco-Ayala, Inés Gómez-Seguí, Guillermo Sanz & Pilar Solves * Centro de
Investigación Biomédica en Red de Cáncer, CIBERONC, Instituto de Salud Carlos III, Madrid, Spain Inés Gómez-Seguí, Guillermo Sanz & Pilar Solves Authors * Javier Marco-Ayala View author
publications You can also search for this author inPubMed Google Scholar * Inés Gómez-Seguí View author publications You can also search for this author inPubMed Google Scholar * Guillermo
Sanz View author publications You can also search for this author inPubMed Google Scholar * Pilar Solves View author publications You can also search for this author inPubMed Google Scholar
CORRESPONDING AUTHOR Correspondence to Javier Marco-Ayala. ETHICS DECLARATIONS CONFLICT OF INTEREST The authors declare that they have no conflict of interest. ADDITIONAL INFORMATION
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THIS ARTICLE CITE THIS ARTICLE Marco-Ayala, J., Gómez-Seguí, I., Sanz, G. _et al._ Pure red cell aplasia after major or bidirectional ABO incompatible hematopoietic stem cell
transplantation: to treat or not to treat, that is the question. _Bone Marrow Transplant_ 56, 769–778 (2021). https://doi.org/10.1038/s41409-020-01124-6 Download citation * Received: 08 May
2020 * Revised: 19 October 2020 * Accepted: 30 October 2020 * Published: 14 November 2020 * Issue Date: April 2021 * DOI: https://doi.org/10.1038/s41409-020-01124-6 SHARE THIS ARTICLE Anyone
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