Red Cell Depletion of Major ABO Incompatible Bone Marrow Hematopoietic Progenitor Cells HPC(M) with the Spectra Optia®.


Journal

Annals of clinical and laboratory science
ISSN: 1550-8080
Titre abrégé: Ann Clin Lab Sci
Pays: United States
ID NLM: 0410247

Informations de publication

Date de publication:
Nov 2020
Historique:
entrez: 18 12 2020
pubmed: 19 12 2020
medline: 12 6 2021
Statut: ppublish

Résumé

Major ABO incompatible hematopoietic progenitors from bone marrow (HPC(M)) donor collections that are destined for clinical transplantation are typically processed to deplete products of red blood cells (RBCs). The purpose of this study was to compare RBC depletion when using the Spectra Optia® relative to a 2-step method involving a COBE2991 instrument to obtain a buffy coat followed by a hydroxyethyl starch (HES) density gradient (COBE+HES) of the buffy coat. Post-processing recoveries of products undergoing 4, 8, and 10 bone marrow processing (BMP) cycles (i.e. 1 cycle=1 volume of HPC(M)) with the Spectra Optia® were determined for volume, RBC content, viable total nucleated cells (vTNC), viable CD34+ cells (vCD34), viable CD3+ cells (vCD3) and colony-forming-cells (CFC). Subsequent RBC depletions with Spectra Optia® were then performed with 10 BMP cycles on additional HPC(M) collections and were compared against a retrospective analysis of historical COBE+HES post-processing data. Ten BMP cycles of HPC(M) (n=6) products were identified as optimal with volume reductions of 81.3±1.6 % and RBC reductions of 97.0±0.6 % with the Spectra Optia®. This also resulted in an average of 0.28 ±0.14 mL of RBC/kg (mean±SD; n=6) with vTNC yields of 65.0±10.9%, vCD34+ yields of 98.5±12.7%, and vCD3+ yields of 90.6±10.0%. Recoveries with the COBE+HES methodology resulted in vTNC recoveries of 62.9±20.5% (mean±SD; n=30) and 0.63±0.71 mL of RBC/kg (mean±SD; n=30). The Spectra Optia® is a viable option for depleting HPC(M) harvests of contaminating RBC in situations of ABO incompatibility. Target cells from a MNC rich fractionation were preserved through processing while eliminating RBC contaminants.

Identifiants

pubmed: 33334794
pii: 50/6/781

Substances chimiques

ABO Blood-Group System 0

Types de publication

Comparative Study Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

781-789

Informations de copyright

© 2020 by the Association of Clinical Scientists, Inc.

Auteurs

Austin Christensen (A)

University of Utah Cell Therapy and Regenerative Medicine Facility austin.christensen@hsc.utah.edu.

FenFen Hsieh (F)

University of Utah Cell Therapy and Regenerative Medicine Facility.

Michael Boyer (M)

University of Utah Cell Therapy and Regenerative Medicine Facility.
University of Utah Division of Hematology and Hematologic Malignancies, Salt Lake City, UT, USA.

Daniel Couriel (D)

University of Utah Cell Therapy and Regenerative Medicine Facility.
University of Utah Division of Hematology and Hematologic Malignancies, Salt Lake City, UT, USA.

Jo-Anna Reems (JA)

University of Utah Cell Therapy and Regenerative Medicine Facility.
University of Utah Division of Hematology and Hematologic Malignancies, Salt Lake City, UT, USA.

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Classifications MeSH