Polyclonal hematopoiesis with variable telomere shortening in human long-term allogeneic marrow graft recipients

Author:

Mathioudakis George1,Storb Rainer1,McSweeney Peter A.1,Torok-Storb Beverly1,Lansdorp Peter M.1,Brümmendorf Tim H.1,Gass M. John1,Bryant Eileen M.1,Storek Jan1,Flowers Mary E. D.1,Gooley Ted1,Nash Richard A.1

Affiliation:

1. From the Fred Hutchinson Cancer Research Center and the University of Washington School of Medicine, Seattle, WA; and The Terry Fox Laboratory, Vancouver, BC, Canada.

Abstract

Abstract Donor-derived hematopoiesis was assessed in 17 patients who received allogeneic marrow grafts from HLA-matched siblings between 1971 and 1980. Complete blood counts were normal or near normal in all patients except one. Chimerism analyses, using either dual-color XY-chromosome fluorescence in situ hybridization (FISH) or analysis of variable number tandem repeat loci, indicated that 15 out of 16 patients had greater than 97% donor-derived hematopoiesis, whereas 1 patient had indeterminate chimerism. All 12 recipients of grafts from female donors exhibited polyclonal hematopoiesis by X-linked clonal analysis with the use of molecular probes. Of the 17 recipients, 9 exhibited a less than 1.0-kilobase shortening of granulocyte telomere length compared with their respective donors, according to terminal restriction fragment analysis or flow-FISH with a fluorescein-labeled peptide nucleic acid probe. These data suggest that under standard transplantation conditions, the stem cell proliferative potential is not compromised during hematopoietic reconstitution.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

Reference28 articles.

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