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Porcine Liver Transplantation Without Veno-Venous Bypass As an Extended Criteria Donor Model
Published on: August 17, 2022
Haploidentical donor transplants for severe aplastic anemia
Andrea Bacigalupo1, Sabrina Giammarco1
1Department of Hematology, Fondazione Policlinico Universitario Gemelli IRCCS, Universita' Cattolica del Sacro Cuore, Roma, Italy.
Haploidentical stem cell transplantation (HAPLO) shows promise for acquired severe aplastic anemia, with low rejection rates and high survival. This review covers strategies to improve outcomes in HAPLO grafts.
Area of Science:
- Hematology
- Immunology
- Transplantation Medicine
Background:
- Haploidentical stem cell transplantation (HAPLO) is an emerging option for acquired severe aplastic anemia.
- Graft rejection and graft-versus-host disease (GvHD) are significant challenges in HAPLO.
Purpose of the Study:
- To review the current status and outcomes of HAPLO grafts in acquired severe aplastic anemia.
- To discuss strategies for overcoming transplant-related complications.
Main Methods:
- Review of published reports on HAPLO for acquired severe aplastic anemia.
- Analysis of conditioning regimens, graft sources, graft manipulation, and GvHD prophylaxis strategies.
- Inclusion of data on mesenchymal stem cell use.
Main Results:
- Data from 375 patients reviewed.
- Average graft rejection rate of 6%.
- Grade II-IV GvHD observed in 23% of patients.
- 1-year survival rate of 80%.
Conclusions:
- HAPLO transplantation offers encouraging results for acquired severe aplastic anemia, particularly in younger populations.
- Various strategies, including T-cell depletion and post-transplant cyclophosphamide, improve HAPLO outcomes.
- HAPLO transplant is a viable alternative donor option for acquired aplastic anemia.
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