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Updated: Jan 23, 2026

Mouse Kidney Transplantation: Models of Allograft Rejection
Published on: October 11, 2014
Is human leukocyte antigen-matched sibling donor transplant always better than haploidentical allograft?
Ying-Jun Chang1, Xiao-Jun Huang2
1Peking University People's Hospital and Peking University Institute of Hematology, Beijing Key Laboratory of Hematopoietic Stem Cell Transplantation, Xicheng District, Beijing, China.
Currently, haploidentical donor has been an alternative source of stem cell allografts for patients who have no human leukocyte antigen-matched sibling donor or unrelated donors. A number of studies indicated that treating hematological malignancy patients with haploidentical stem cell transplantation (haplo-SCT) could achieve comparable outcomes to those who underwent matched sibling donor transplantation (MSDT). In recent years, more and more evidence support the notion that haploidentical allografts may have a stronger graft-vs-leukemia (GVL) effect than MSDT. In this review, we summarized the transplant outcomes of haplo-SCT and MSDT, mainly focusing on the subgroup of patients who will benefit from the stronger GVL effects of haplo-SCT compared with MSDT. We also offered strategies of how to translate the strong antileukemia activity of haploidentical allograft into superior survival. Future directions of GVL effects in haplo-SCT settings were also discussed.
Currently, haploidentical donor has been an alternative source of stem cell allografts for patients who have no human leukocyte antigen-matched sibling donor or unrelated donors. A number of studies indicated that treating hematological malignancy patients with haploidentical stem cell transplantation (haplo-SCT) could achieve comparable outcomes to those who underwent matched sibling donor transplantation (MSDT). In recent years, more and more evidence support the notion that haploidentical allografts may have a stronger graft-vs-leukemia (GVL) effect than MSDT. In this review, we summarized the transplant outcomes of haplo-SCT and MSDT, mainly focusing on the subgroup of patients who will benefit from the stronger GVL effects of haplo-SCT compared with MSDT. We also offered strategies of how to translate the strong antileukemia activity of haploidentical allograft into superior survival. Future directions of GVL effects in haplo-SCT settings were also discussed.
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