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

Coco de Koning, Weiyang Tao, Amelia Lacna, Karin van Veghel, Mitchell E Horwitz, Guillermo Sanz, Madan H Jagasia, John E Wagner, Patrick J Stiff, Rabi Hanna, Daniela Cilloni, David Valcárcel, Tony Peled, Einat Galamidi Cohen, Uri Goshen, Aridaman Pandit, Caroline A Lindemans, Jaap Jan Boelens, Stefan Nierkens

Journal: Bone marrow transplantation 2022;56(11):2826-2833

PMID: 34312498

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 × 10/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).

Address: University Medical Center Utrecht, Utrecht, The Netherlands.; Princess Máxima Center for Pediatric Oncology, Utrecht, The Netherlands.; University Medical Center Utrecht, Utrecht, The Netherlands.; Duke University Medical Center, Durham, NC, USA.; Hospital Universitario y Politécnico la Fe, València, Spain.; Centro de Investigación Biomédica en Red de Cáncer, CIBERONC, Instituto de Salud Carlos III, Madrid, Spain.; Vanderbilt University Medical Center, Nashville, TN, USA.; University of Minnesota, Minneapolis, MN, USA.; Loyola University Medical Center, Chicago, IL, USA.; Cleveland Clinic, Cleveland, OH, USA.; University of Turin, Turin, Italy.; University Hospital Vall d'Hebron, Barcelona, Spain.; Gamida Cell. Ltd, Jerusalem, Israel.; Princess Máxima Center for Pediatric Oncology, Utrecht, The Netherlands.; Memorial Sloan Kettering Cancer Center, New York, NY, USA.; University Medical Center Utrecht, Utrecht, The Netherlands. [email protected].; Princess Máxima Center for Pediatric Oncology, Utrecht, The Netherlands. [email protected].
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