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Haploidentical hematopoietic stem cell transplantation in adults using the αβTCR/CD19-based depletion of G-CSF-mobilized peripheral blood progenitor cells

Abstract

In patients with hematological malignancies at high risk for relapse, a mismatched hematopoietic stem cells transplants can be offered with no undue delay between decision-making and transplantation as virtually all patients have a full-haplotype mismatched member who could serve immediately as a donor. Using a T-cell depletion approach, these patients can benefit from a graft-vs-leukemia effect in the absence of both acute and chronic graft-vs-host disease. Over the past decade, efforts have concentrated on developing new conditioning regimens, optimizing the graft processing and improving the posttransplant immunological recovery. The innovative strategy based on the selective depletion of alpha/beta-positive T lymphocytes from G-CSF-mobilized peripheral blood precursor cells has shown very promising results in the setting of the pediatric transplantation. This paper reports the outcome in adult patients with hematological malignancies.

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Funding

Publication of this supplement was sponsored by the Gilead Sciences Europe Ltd., Cell Source, Inc., The Chorafas Institute for Scientific Exchange of the Weizmann Institute of Science, Kiadis Pharma, Miltenyi Biotec, Celgene, Centro Servizi Congressuali, Almog Diagnostic.

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Correspondence to Franco Aversa.

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FR received lecture fees from Gilead. MC received lecture fees from Novartis, Incyte, and Janssen. NG received consulting fees from Janssen, Celgene, Takeda, Amgen; lecture fees from Janssen, Celgene, Bristol Myers Squibb; and grant support from Janssen Pharmaceuticals, Millennium Pharmaceuticals (Takeda Oncology), and GlaxoSmithKline S.p.A. FA received lecture fees from Gilead, Basilea, Novartis, MSD, Kaidis, and Pfizer. The remaining authors declared no competing interest.

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Prezioso, L., Manfra, I., Bonomini, S. et al. Haploidentical hematopoietic stem cell transplantation in adults using the αβTCR/CD19-based depletion of G-CSF-mobilized peripheral blood progenitor cells. Bone Marrow Transplant 54 (Suppl 2), 698–702 (2019). https://doi.org/10.1038/s41409-019-0608-z

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