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A Novel Approach for the Enumeration of Peripheral Blood Stem Cells Suitable for Transplantation

DOI: 10.1155/2014/473503

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Abstract:

Stem cells have the capability to proliferate and differentiate into various cells of the body. Few stem cell sources have been approved for transplantation, among them are the hematopoietic progenitor cells which are progenitors of the myeloid and erythroid lineage in the hematopoietic system, that continually provides mature blood cells during the lifespan of the individual. These well-characterized stem cells are clinically relevant in the treatment of diseases such as breast cancer, leukemias, and congenital immunodeficiencies. Peripheral blood stem transplantation is a standard procedure after its first successful transplantation more than 35 years ago. The minimum intended dose of stem cells given to the patient is cells. In this study, we are establishing a correlation between the number of stem cells enumerated and the weight of the patient as a determinant for suitable transplantation. We have established a conversion factor to deliver the required dose of approximately stem cells/kg body weight. This will ensure a uniform collection strategy that is sufficient for transplantation irrespective of the weight of the patient. This approach, if incorporated, will lead to a significantly lesser rate of bone marrow transplantation failures as sufficient number of stem cells will ensure engraftment of stem cells. 1. Introduction Peripheral blood-derived stem cells (PBSCs) have been used in bone marrow transplantation ever since its first report was published in the late ‘70s [1]. In recent years, there has been rapid expansion of the clinical use of hematopoietic stem cells as well as its concomitant understanding of its basic biology. These stem cells, which are a critical component of transplantation, are progenitors to the blood cells of the body that constitutes the myeloid and erythroid lineage [2]. They continuously provide mature blood cells during the lifespan of the individual. These are one of the best characterized stem cells in the body that are clinically applicable in the treatment of diseases such as breast cancer, leukemias, and congenital immunodeficiencies [3]. Hematopoietic stem cells (HSCs) belong to a group of multipotent precursors that have a self-renewal capacity and the ability to generate different cell types that comprise of the blood-forming system [4]. Transplantation of HSCs forms the basis of consolidation therapy in cancer treatments and is used to cure or ameliorate a number of hematologic and genetic disorders [5]. HSCs are also an attractive target cell population for gene therapies because they are readily

References

[1]  J. M. Goldman, K. H. Th'ng, D. S. Park, A. S. Spiers, R. M. Lowenthal, and T. Ruutu, “Collection, cryopreservation and subsequent viability of haemopoietic stem cells intended for treatment of chronic granulocytic leukaemia in blast-cell transformation,” British Journal of Haematology, vol. 40, no. 2, pp. 185–195, 1978.
[2]  A. Trumpp, M. Essers, and A. Wilson, “Awakening dormant haematopoietic stem cells,” Nature Reviews Immunology, vol. 10, no. 3, pp. 201–209, 2010.
[3]  M. Kondo, A. J. Wagers, M. G. Manz et al., “Biology of hematopoietic stem cells and progenitors: implications for clinical application,” Annual Review of Immunology, vol. 21, pp. 759–806, 2003.
[4]  A. E. Bishop, L. D. K. Buttery, and J. M. Polak, “Haematopoietic stem cells,” Journal of Pathology, vol. 197, no. 4, pp. 430–440, 2002.
[5]  J. A. Shizuru, R. S. Negrin, and I. L. Weissman, “Hematopoietic stem and progenitor cells: clinical and preclinical regeneration of the hematolymphoid system,” Annual Review of Medicine, vol. 56, pp. 509–538, 2005.
[6]  R. G. Hawley, “Progress toward vector design for hematopoietic stem cell gene therapy,” Current Gene Therapy, vol. 1, no. 1, pp. 1–17, 2001.
[7]  S. Siena, R. Schiavo, P. Pedrazzoli, and C. Carlo-Stella, “Therapeutic relevance of CD34+ cell dose in blood cell transplantation for cancer therapy,” Journal of Clinical Oncology, vol. 18, no. 6, pp. 1360–1377, 2000.
[8]  L. B. To, D. N. Haylock, P. J. Simmons, and C. A. Juttner, “The biology and clinical uses of blood stem cells,” Blood, vol. 89, no. 7, pp. 2233–2258, 1997.
[9]  D. R. Sutherland, L. Anderson, M. Keeney, R. Nayar, and I. Chin-Yee, “The ISHAGE guidelines for CD34+ cell determination by flow cytometry,” Journal of Hematotherapy and Stem Cell Research, vol. 5, no. 3, pp. 213–226, 1996.
[10]  S. Massberg and U. H. von Andrian, “Novel trafficking routes for hematopoietic stem and progenitor cells,” Annals of the New York Academy of Sciences, vol. 1176, pp. 87–93, 2009.
[11]  A. Spradling, D. Drummond-Barbosa, and T. Kai, “Stem cells find their niche,” Nature, vol. 414, no. 6859, pp. 98–104, 2001.
[12]  I. Petit, M. Szyper-Kravitz, A. Nagler et al., “G-CSF induces stem cell mobilization by decreasing bone marrow SDF-1 and up-regulating CXCR4,” Nature Immunology, vol. 3, no. 7, pp. 687–694, 2002.
[13]  W. I. Bensinger, T. H. Price, D. C. Dale et al., “The effects of daily recombinant human granulocyte colony-stimulating factor administration on normal granulocyte donors undergoing leukapheresis,” Blood, vol. 81, no. 7, pp. 1883–1889, 1993.
[14]  P. Anderlini, D. Przepiorka, J. Lauppe et al., “Collection of peripheral blood stem cells from normal donors 60 years of age or older,” British Journal of Haematology, vol. 97, no. 2, pp. 485–487, 1997.
[15]  T. Lapidot, A. Dar, and O. Kollet, “How do stem cells find their way home?” Blood, vol. 106, no. 6, pp. 1901–1910, 2005.
[16]  H. Baldomero, M. Gratwohl, A. Gratwohl et al., “The EBMT activity survey 2009: trends over the past 5 years,” Bone Marrow Transplantation, vol. 46, no. 4, pp. 485–501, 2011.
[17]  A. Gratwohl and H. Baldomero, “Trends of hematopoietic stem cell transplantation in the third millennium,” Current Opinion in Hematology, vol. 16, no. 6, pp. 420–426, 2009.
[18]  Y. Cohen and A. Nagler, “Umbilical cord blood transplantation—how, when and for whom?” Blood Reviews, vol. 18, no. 3, pp. 167–179, 2004.
[19]  W. Bensinger, F. Appelbaum, S. Rowley et al., “Factors that influence collection and engraftment of autologous peripheral-blood stem cells,” Journal of Clinical Oncology, vol. 13, no. 10, pp. 2547–2555, 1995.
[20]  K. R. Desikan, G. Tricot, N. C. Munshi et al., “Preceding chemotherapy, tumour load and age influence engraftment in multiple myeloma patients mobilized with granulocyte colony-stimulating factor alone,” British Journal of Haematology, vol. 112, no. 1, pp. 242–247, 2001.
[21]  C. H. Weaver, B. Hazelton, R. Birch et al., “An analysis of engraftment kinetics as a function of the CD34+ content of peripheral blood progenitor cell collections in 692 patients after the administration of myeloablative chemotherapy,” Blood, vol. 86, no. 10, pp. 3961–3969, 1995.
[22]  N. Ketterer, G. Salles, M. Raba et al., “High CD34+ cell counts decrease hematologic toxicity of autologous peripheral blood progenitor cell transplantation,” Blood, vol. 91, no. 9, pp. 3148–3155, 1998.
[23]  S. Giralt, E. A. Stadtmauer, J. L. Harousseau et al., “International myeloma working group (IMWG) consensus statement and guidelines regarding the current status of stem cell collection and high-dose therapy for multiple myeloma and the role of plerixafor (AMD 3100),” Leukemia, vol. 23, no. 10, pp. 1904–1912, 2009.
[24]  J. M. Sancho, M. Morgades, J. R. Grifols et al., “Predictive factors for poor peripheral blood stem cell mobilization and peak CD34+ cell count to guide pre-emptive or immediate rescue mobilization,” Cytotherapy, vol. 14, no. 7, pp. 823–829, 2012.
[25]  S. Fu and J. Liesveld, “Mobilization of hematopoietic stem cells,” Blood Reviews, vol. 14, no. 4, pp. 205–218, 2000.

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