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4 - Stem Cell Source

Published online by Cambridge University Press:  23 November 2009

Joseph H. Antin
Affiliation:
Dana-Farber Cancer Institute, Boston
Deborah Yolin Raley
Affiliation:
Dana-Farber Cancer Institute, Boston
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Summary

HEMATOPOIETIC PROGENITOR CELL PRODUCTS

Hematopoietic progenitor cell (HPC) products contain hematopoietic stem and lineage-committed progenitor cells capable of providing hematopoietic and immune reconstitution after myeloablative or reduced-intensity preparative regimens. There is no unanimity on the terminology.

  • Since stem cells are difficult to specifically identify, some authors prefer the term hematopoietic cell transplantation (HCT).

  • Others call the procedure hematopoietic stem cell transplantation (HSCT) to acknowledge that most transplantations are not successful unless stem cells are transplanted.

  • The Foundation For The Accreditation of Cellular Therapy (FACT) focuses on progenitors. Cellular therapy products can be broadly categorized as being minimally manipulated products and more than minimally manipulated products.

Hematopoietic Progenitor Cell Function

Hematopoietic progenitor cells (HPCs) administered intravenously migrate to the marrow, where they adhere, expand, selfrenew (stem cells only), and differentiate. The differentiated cells are released into the blood, restoring blood counts and immunity. The time from administration of HPCs to recovery of adequate or normal blood counts is variable (see section on Engraftment).

Indications

Allogeneic HPC products are intended to provide hematopoietic reconstitution after myeloablative or reduced intensity preparative regimens for a wide range of disease states. For some patients the product is also intended to provide a graft-versus-tumor effect. Autologous HPCs are collected and stored for use as a “rescue” following myeloablative or severely myelotoxic therapy. The high-dose therapy is intended to treat the patient's underlying malignancy and autologous HPC products are administered to minimize morbidity and mortality due to the myelotoxic effects of the therapy.

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Publisher: Cambridge University Press
Print publication year: 2009

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