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Augmentation of Donor Bone Marrow Engraftment in Histoincompatible Murine Recipients by Granulocyte/Macrophage Colony-Stimulating Factor
Blood, 1988-02, Vol.71 (2), p.320-328
Blazar, Bruce R.
Widmer, Michael B.
Soderling, Christine C.B.
Urdal, David L.
Gillis, Steven
Robison, Leslie L.
Vallera, Daniel A.
1988
Volltextzugriff (PDF)
Details
Autor(en) / Beteiligte
Blazar, Bruce R.
Widmer, Michael B.
Soderling, Christine C.B.
Urdal, David L.
Gillis, Steven
Robison, Leslie L.
Vallera, Daniel A.
Titel
Augmentation of Donor Bone Marrow Engraftment in Histoincompatible Murine Recipients by Granulocyte/Macrophage Colony-Stimulating Factor
Ist Teil von
Blood, 1988-02, Vol.71 (2), p.320-328
Ort / Verlag
Washington, DC: Elsevier Inc
Erscheinungsjahr
1988
Quelle
MEDLINE
Beschreibungen/Notizen
T cell depletion of donor bone marrow can prevent graft v host disease (GVHD) in human and murine marrow graft recipients. However, engraftment in the recipient may be compromised as a consequence of donor marrow T cell depletion. The effect of recombinant murine granulocyte/ macrophage colony-stimulating factor (rmu GM-CSF) on engraftment and hematologic reconstitution was evaluated in a murine allogeneic bone marrow transplantation (BMT) model involving T cell depletion of marrow. Before transplantation into irradiated mice differing at major and minor histocompatibility loci, rmu GM-CSF was preincubated with T cell-depleted donor marrow. When low degrees of engraftment were noted in control recipients, treatment of donor marrow with high concentrations of rmu GM-CSF led to enhanced engraftment. Ex vivo donor graft incubation with rmu GM-CSF or a single in vivo injection of rmu GM-CSF were both effective means of promoting engraftment. When the engraftment rate in control recipients was high, rmu GM-CSF did not have an identifiable effect. Only slight increases in hematologic recovery were detected regardless of the rate of engraftment. Neither post-BMT survival nor marrow stem cell capacity was affected by rmu GM-CSF incubation. Furthermore, growth factor administration did not have a significant effect on the incidence of GVHD in recipients of non-T cell-depleted bone marrow/ splenocyte preparations. In vitro natural killer-mediated target cell lysis was not altered by incubation of effector cells with rmu GM-CSF. These results demonstrate the potential of ex vivo rmu GM-CSF treatment of donor marrow to facilitate engraftment across extensive histocompatibility barriers.©1988 by Grune & Stratton, Inc. 0006-4971/88/7102-0002S3.00/0
Sprache
Englisch
Identifikatoren
ISSN: 0006-4971
eISSN: 1528-0020
DOI: 10.1182/blood.V71.2.320.320
Titel-ID: cdi_proquest_miscellaneous_78084601
Format
–
Schlagworte
Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy
,
Animals
,
Biological and medical sciences
,
Bone Marrow Transplantation
,
Bone marrow, stem cells transplantation. Graft versus host reaction
,
Colony-Stimulating Factors - therapeutic use
,
Graft vs Host Disease - etiology
,
Graft vs Host Disease - immunology
,
Granulocyte-Macrophage Colony-Stimulating Factor
,
Growth Substances - therapeutic use
,
Hematopoietic Stem Cells - drug effects
,
In Vitro Techniques
,
Killer Cells, Natural - immunology
,
Medical sciences
,
Mice
,
Mice, Inbred Strains
,
Recombinant Proteins - therapeutic use
,
T-Lymphocytes - immunology
,
Time Factors
,
Transfusions. Complications. Transfusion reactions. Cell and gene therapy
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