Lymphoid and myeloid immune cell reconstitution after nicotinamide-expanded cord blood transplantation Journal Article


Authors: de Koning, C.; Tao, W.; Lacna, A.; van Veghel, K.; Horwitz, M. E.; Sanz, G.; Jagasia, M. H.; Wagner, J. E.; Stiff, P. J.; Hanna, R.; Cilloni, D.; Valcárcel, D.; Peled, T.; Galamidi Cohen, E.; Goshen, U.; Pandit, A.; Lindemans, C. A.; Boelens, J. J.; Nierkens, S.
Article Title: Lymphoid and myeloid immune cell reconstitution after nicotinamide-expanded cord blood transplantation
Abstract: Omidubicel (nicotinamide-expanded cord blood) is a potential alternative source for allogeneic hematopoietic cell transplantation (HCT) when an HLA-identical donor is lacking. A phase I/II trial with standalone omidubicel HCT showed rapid and robust neutrophil and platelet engraftment. In this study, we evaluated the immune reconstitution (IR) of patients receiving omidubicel grafts during the first 6 months post-transplant, as IR is critical for favorable outcomes of the procedure. Data was collected from the omidubicel phase I-II international, multicenter trial. The primary endpoint was the probability of achieving adequate CD4+ T-cell IR (CD4IR: > 50 × 106/L within 100 days). Secondary endpoints were the recovery of T-cells, natural killer (NK)-cells, B-cells, dendritic cells (DC), and monocytes as determined with multicolor flow cytometry. LOESS-regression curves and cumulative incidence plots were used for data description. Thirty-six omidubicel recipients (median 44; 13–63 years) were included, and IR data was available from 28 recipients. Of these patients, 90% achieved adequate CD4IR. Overall, IR was complete and consisted of T-cell, monocyte, DC, and notably fast NK- and B-cell reconstitution, compared to conventional grafts. Our data show that transplantation of adolescent and adult patients with omidubicel results in full and broad IR, which is comparable with IR after HCT with conventional graft sources. © 2021, The Author(s).
Journal Title: Bone Marrow Transplantation
Volume: 56
Issue: 11
ISSN: 0268-3369
Publisher: Nature Publishing Group  
Date Published: 2021-11-01
Start Page: 2826
End Page: 2833
Language: English
DOI: 10.1038/s41409-021-01417-4
PUBMED: 34312498
PROVIDER: scopus
PMCID: PMC8563413
DOI/URL:
Notes: Article -- Export Date: 1 December 2021 -- Source: Scopus
Altmetric
Citation Impact
BMJ Impact Analytics
MSK Authors
  1. Jaap Jan Boelens
    211 Boelens