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Tytuł pozycji:

Evaluation of leukaemic contamination in peripheral blood stem cell harvests by reverse transcriptase polymerase chain reaction.

Tytuł:
Evaluation of leukaemic contamination in peripheral blood stem cell harvests by reverse transcriptase polymerase chain reaction.
Autorzy:
Nagafuji K; First Department of Internal Medicine, Faculty of Medicine, Kyushu University, Fukuoka, Japan.
Harada M
Takamatsu Y
Eto T
Teshima T
Kamura T
Okamura T
Hayashi S
Akashi K
Murakawa M
et. al.
Źródło:
British journal of haematology [Br J Haematol] 1993 Nov; Vol. 85 (3), pp. 578-83.
Typ publikacji:
Comparative Study; Journal Article; Research Support, Non-U.S. Gov't
Język:
English
Imprint Name(s):
Publication: Oxford : Wiley-Blackwell
Original Publication: Oxford : Blackwell Scientific Publications
MeSH Terms:
Blood Transfusion, Autologous*
Hematopoietic Stem Cell Transplantation*
Leukemia/*blood
Neoplastic Stem Cells/*pathology
Adult ; Base Sequence ; Bone Marrow/pathology ; Female ; Humans ; Leukemia/therapy ; Male ; Middle Aged ; Molecular Sequence Data ; Polymerase Chain Reaction ; RNA, Messenger/analysis ; RNA, Neoplasm/analysis ; RNA-Directed DNA Polymerase
Substance Nomenclature:
0 (RNA, Messenger)
0 (RNA, Neoplasm)
EC 2.7.7.49 (RNA-Directed DNA Polymerase)
Entry Date(s):
Date Created: 19931101 Date Completed: 19940422 Latest Revision: 20190705
Update Code:
20240104
DOI:
10.1111/j.1365-2141.1993.tb03351.x
PMID:
7510991
Czasopismo naukowe
A major issue in autologous blood stem cell transplantation (ABSCT) for leukaemia is whether peripheral blood stem cell (PBSC) harvests are less contaminated with leukaemic cells than bone marrow mononuclear cells (BMMNC). We compared leukaemic contamination in PBSC harvests and BMMNC, obtained simultaneously, by using reverse transcriptase polymerase chain reaction (RT-PCR) of leukaemia-specific chimaeric messenger RNA (mRNA), in three patients with Philadelphia chromosome (Ph)-positive acute lymphoblastic leukaemia (ALL), one with Ph-positive acute myelogenous leukaemia (AML), and two with acute promyelocytic leukaemia (APL). Our two-step PCR method employed 'nested primers' in the second step and can detect one leukaemic blast diluted into 10(6) HL-60 cells. In three of four patients with Ph-positive ALL and AML we detected leukaemic contamination in both PBSC harvests and BMMNC. In the remaining patient with ALL, both PBSC harvests and BMMNC were PCR-negative. Both PBSC harvests and BMMNC from one patient with APL were PCR-positive. In contrast, PBSC harvests from another patient with APL, whose BMMNC could not be obtained because of bone marrow necrosis, were PCR-positive after the first course of consolidation chemotherapy, but became PCR-negative after the second course. The present study does not support the hypothesis that PBSC harvests are less contaminated by leukaemic cells than BMMNC, but suggests that PBSC harvests are contaminated when BMMNC are contaminated.

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