Optimizing haematopoietic stem and progenitor cell apheresis collection from plerixafor-mobilized patients with sickle cell disease.


Journal

British journal of haematology
ISSN: 1365-2141
Titre abrégé: Br J Haematol
Pays: England
ID NLM: 0372544

Informations de publication

Date de publication:
08 2022
Historique:
revised: 23 05 2022
received: 15 04 2022
accepted: 01 06 2022
pubmed: 24 6 2022
medline: 10 8 2022
entrez: 23 6 2022
Statut: ppublish

Résumé

We adjusted haematopoietic stem and progenitor cell (HSPC) apheresis collection from patients with sickle cell disease (SCD) by targeting deep buffy coat collection using medium or low collection preference (CP), and by increasing anticoagulant-citrate-dextrose-solution A dosage. In 43 HSPC collections from plerixafor-mobilized adult patients with SCD, we increased the collection efficiency to 35.79% using medium CP and 82.23% using low CP. Deep buffy coat collection increased red blood cell contamination of the HSPC product, the product haematocrit was 4.7% with medium CP and 6.4% with low CP. These adjustments were well-tolerated and allowed efficient HSPC collection from SCD patients.

Identifiants

pubmed: 35737751
doi: 10.1111/bjh.18311
doi:

Substances chimiques

Benzylamines 0
Cyclams 0
Heterocyclic Compounds 0
plerixafor S915P5499N

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

740-744

Informations de copyright

© 2022 British Society for Haematology and John Wiley & Sons Ltd.

Références

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Esrick EB, Manis JP, Daley H, Baricordi C, Trebeden-Negre H, Pierciey FJ, et al. Successful hematopoietic stem cell mobilization and apheresis collection using plerixafor alone in sickle cell patients. Blood Adv. 2018;2(19):2505-12.
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Auteurs

Akshay Sharma (A)

Department of Bone Marrow Transplantation and Cellular Therapy, St. Jude Children's Research Hospital, Memphis, Tennessee, USA.

Alexis Leonard (A)

Cellular and Molecular Therapeutics Branch, National Heart, Lung, and Blood Institute (NHLBI), National Institutes of Health, Bethesda, Maryland, USA.

Kamille West (K)

Cell Processing Section, Department of Transfusion Medicine, Clinical Center, National Institutes of Health, Bethesda, Maryland, USA.

Jeffrey M Gossett (JM)

Department of Biostatistics, St. Jude Children's Research Hospital, Memphis, Tennessee, USA.

Naoya Uchida (N)

Cellular and Molecular Therapeutics Branch, National Heart, Lung, and Blood Institute (NHLBI), National Institutes of Health, Bethesda, Maryland, USA.

Sandhya Panch (S)

Cell Processing Section, Department of Transfusion Medicine, Clinical Center, National Institutes of Health, Bethesda, Maryland, USA.

David Stroncek (D)

Cell Processing Section, Department of Transfusion Medicine, Clinical Center, National Institutes of Health, Bethesda, Maryland, USA.

Leigh Poston (L)

Human Applications Lab, St. Jude Children's Research Hospital, Memphis, Tennessee, USA.

Salem Akel (S)

Human Applications Lab, St. Jude Children's Research Hospital, Memphis, Tennessee, USA.

Jane S Hankins (JS)

Department of Hematology, St. Jude Children's Research Hospital, Memphis, Tennessee, USA.

Courtney Fitzhugh (C)

Cellular and Molecular Therapeutics Branch, National Heart, Lung, and Blood Institute (NHLBI), National Institutes of Health, Bethesda, Maryland, USA.

Matthew M Hsieh (MM)

Cellular and Molecular Therapeutics Branch, National Heart, Lung, and Blood Institute (NHLBI), National Institutes of Health, Bethesda, Maryland, USA.

Guolian Kang (G)

Department of Biostatistics, St. Jude Children's Research Hospital, Memphis, Tennessee, USA.

John F Tisdale (JF)

Cellular and Molecular Therapeutics Branch, National Heart, Lung, and Blood Institute (NHLBI), National Institutes of Health, Bethesda, Maryland, USA.

Mitchell J Weiss (MJ)

Department of Hematology, St. Jude Children's Research Hospital, Memphis, Tennessee, USA.

Yan Zheng (Y)

Department of Pathology, St. Jude Children's Research Hospital, Memphis, Tennessee, USA.

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