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Updated: Mar 13, 2026

Generation of Multivirus-specific T Cells to Prevent/treat Viral Infections after Allogeneic Hematopoietic Stem Cell Transplant
Published on: May 27, 2011
Current role of ATG in GVHD prevention: optimizing post-transplantation outcomes through combination with PTCY
Maria Liga1, Dimitrios Tsokanas1, Angeliki N Georgopoulou1
1Hematology Division and Bone Marrow Transplantation Unit, Institute of Cell Therapy, University of Patras, Rio 26504, Greece.
Graft versus host disease (GVHD) is one of the major complications of allogeneic hematopoietic cell transplantation (allo-HCT), contributing significantly to post-transplant morbidity and mortality. Anti-thymocyte globulin (ATG) is a widely used GVHD prophylaxis in combination with a calcineurin inhibitor and an antimetabolite. Post-transplant cyclophosphamide (PTCy) has been a milestone in haploidentical transplantation, and its use has expanded to allo-HCT performed from matched related and unrelated donors with notable success. In this review, we discuss how post-transplantation outcomes can be optimized through a combination of ATG with PTCY. We summarize the biological rationale, current clinical evidence, and remaining uncertainties regarding this dual in vivo T-cell depletion strategy, highlighting its potential to enhance GVHD control, reduce immunosuppressive burden, and improve survival across different donor settings.
Graft versus host disease (GVHD) is one of the major complications of allogeneic hematopoietic cell transplantation (allo-HCT), contributing significantly to post-transplant morbidity and mortality. Anti-thymocyte globulin (ATG) is a widely used GVHD prophylaxis in combination with a calcineurin inhibitor and an antimetabolite. Post-transplant cyclophosphamide (PTCy) has been a milestone in haploidentical transplantation, and its use has expanded to allo-HCT performed from matched related and unrelated donors with notable success. In this review, we discuss how post-transplantation outcomes can be optimized through a combination of ATG with PTCY. We summarize the biological rationale, current clinical evidence, and remaining uncertainties regarding this dual in vivo T-cell depletion strategy, highlighting its potential to enhance GVHD control, reduce immunosuppressive burden, and improve survival across different donor settings.
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