Long-term engraftment and clonal dominance of donor-derived del(20q) hematopoietic cells after allogeneic stem cell transplantation [3]

Blood

Volumn 107, Issue 4, 2006, Pages 1732-1733

  Mielcarek, Marco ^a   Bryant, Eileen ^b   Loken, Michael ^b   Zaucha, Jan Maciej ^b   Torok Storb, Beverly ^b   Storb, Rainer ^b  

^a Fred Hutchinson Cancer Research Center   (United States)

^b NONE

Author keywords

[No Author keywords available]

Indexed keywords

CYCLOPHOSPHAMIDE; CYCLOSPORIN; METHOTREXATE;

ADULT; ALLOGENEIC STEM CELL TRANSPLANTATION; B LYMPHOCYTE; BONE MARROW CELL; CASE REPORT; CELL CLONE; CHROMOSOME ANALYSIS; CHROMOSOME DELETION; CHROMOSOME DELETION 20; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; FOLLOW UP; GRAFT VERSUS HOST REACTION; HEMATOPOIETIC CELL; HLA MATCHING; HUMAN; HUMAN CELL; IMMUNOPROPHYLAXIS; IMMUNOSUPPRESSIVE TREATMENT; LETTER; LIVING DONOR; LYMPHOID CELL; MYELODYSPLASTIC SYNDROME; PRIORITY JOURNAL; RECIPIENT; REFRACTORY ANEMIA; REMISSION; SIBLING; T CELL LYMPHOMA; T LYMPHOCYTE; VARIABLE NUMBER OF TANDEM REPEAT; WHOLE BODY RADIATION;

EID: 32644441021     PISSN: 00064971     EISSN: 00064971     Source Type: Journal    
DOI: 10.1182/blood-2005-09-3781     Document Type: Letter

References (5)

1. Mielcarek M, Bryant E, Loken M, Torok-Storb B, Storb R. Haemopoietic reconstitution by donor-derived myelodysplastic progenitor cells after haemopoietic stem cell transplantation. Br J Haematol. 1999;105:361-365.
2. White NJ, Nacheva E, Asimakopoulos FA, Bloxham D, Paul B, Green AR. Deletion of chromosome 20q in myelodysplasia can occur in a multipotent precursor of both myeloid cells and B cells. Blood. 1994;83:2809-2816.
3. van Lom K, Hagemeijer A, Smit E, Hahlen K, Groeneveld K, Lowenberg B. Cytogenetic clonality analysis in myelodysplastic syndrome: monosomy 7 can be demonstrated in the myeloid and in the lymphoid lineage. Leukemia. 1995;9: 1818-1821.
4. van Kamp H, Fibbe WE, Jansen RP, et al. Clonal involvement of granulocytes and monocytes, but not of T and B lymphocytes and natural killer cells in patients with myelodysplasia: analysis by X-linked restriction fragment length polymorphisms and polymerase chain reaction of the phosphoglycerate kinase gene. Blood. 1992;80:1774-1780.
5. Kibbelaar RE, van Kamp H, Dreef EJ, et al. Combined immunophenotyping and DNA in situ hybridization to study lineage involvement in patients with myelodysplastic syndromes. Blood. 1992;79:1823-1828.