author_facet Erlecke, Jörn
Hartmann, Isabell
Hoffmann, Martin
Kroll, Torsten
Starke, Heike
Heller, Anita
Gloria, Alexander
Sayer, Herbert G
Johannes, Tilman
Claussen, Uwe
Liehr, Thomas
Loncarevic, Ivan F
Erlecke, Jörn
Hartmann, Isabell
Hoffmann, Martin
Kroll, Torsten
Starke, Heike
Heller, Anita
Gloria, Alexander
Sayer, Herbert G
Johannes, Tilman
Claussen, Uwe
Liehr, Thomas
Loncarevic, Ivan F
author Erlecke, Jörn
Hartmann, Isabell
Hoffmann, Martin
Kroll, Torsten
Starke, Heike
Heller, Anita
Gloria, Alexander
Sayer, Herbert G
Johannes, Tilman
Claussen, Uwe
Liehr, Thomas
Loncarevic, Ivan F
spellingShingle Erlecke, Jörn
Hartmann, Isabell
Hoffmann, Martin
Kroll, Torsten
Starke, Heike
Heller, Anita
Gloria, Alexander
Sayer, Herbert G
Johannes, Tilman
Claussen, Uwe
Liehr, Thomas
Loncarevic, Ivan F
Molecular Cytogenetics
Automated detection of residual cells after sex-mismatched stem-cell transplantation – evidence for presence of disease-marker negative residual cells
Biochemistry (medical)
Genetics (clinical)
Genetics
Molecular Biology
Molecular Medicine
Biochemistry
author_sort erlecke, jörn
spelling Erlecke, Jörn Hartmann, Isabell Hoffmann, Martin Kroll, Torsten Starke, Heike Heller, Anita Gloria, Alexander Sayer, Herbert G Johannes, Tilman Claussen, Uwe Liehr, Thomas Loncarevic, Ivan F 1755-8166 Springer Science and Business Media LLC Biochemistry (medical) Genetics (clinical) Genetics Molecular Biology Molecular Medicine Biochemistry http://dx.doi.org/10.1186/1755-8166-2-12 <jats:title>Abstract</jats:title> <jats:sec> <jats:title>Background</jats:title> <jats:p>A new chimerism analysis based on automated interphase fluorescence in situ hybridization (FISH) evaluation was established to detect residual cells after allogene sex-mismatched bone marrow or blood stem-cell transplantation.</jats:p> <jats:p>Cells of 58 patients were characterized as disease-associated due to presence of a bcr/abl-gene-fusion or a trisomy 8 and/or a simultaneous hybridization of gonosome-specific centromeric probes. The automatic slide scanning platform Metafer with its module MetaCyte was used to analyse 3,000 cells per sample.</jats:p> </jats:sec> <jats:sec> <jats:title>Results</jats:title> <jats:p>Overall 454 assays of 58 patients were analyzed. 13 of 58 patients showed residual recipient cells at one stage of more than 4% and 12 of 58 showed residual recipient cells less than 4%, respectively. As to be expected, patients of the latter group were associated with a higher survival rate (48 vs. 34 month). In only two of seven patients with disease-marker positive residual cells between 0.1–1.3% a relapse was observed. Besides, disease-marker negative residual cells were found in two patients without relapse at a rate of 2.8% and 3.3%, respectively.</jats:p> </jats:sec> <jats:sec> <jats:title>Conclusion</jats:title> <jats:p>The definite origin and meaning of disease-marker negative residual cells is still unclear. Overall, with the presented automatic chimerism analysis of interphase FISH slides, a sensitive method for detection of disease-marker positive residual cells is on hand.</jats:p> </jats:sec> Automated detection of residual cells after sex-mismatched stem-cell transplantation – evidence for presence of disease-marker negative residual cells Molecular Cytogenetics
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title Automated detection of residual cells after sex-mismatched stem-cell transplantation – evidence for presence of disease-marker negative residual cells
title_unstemmed Automated detection of residual cells after sex-mismatched stem-cell transplantation – evidence for presence of disease-marker negative residual cells
title_full Automated detection of residual cells after sex-mismatched stem-cell transplantation – evidence for presence of disease-marker negative residual cells
title_fullStr Automated detection of residual cells after sex-mismatched stem-cell transplantation – evidence for presence of disease-marker negative residual cells
title_full_unstemmed Automated detection of residual cells after sex-mismatched stem-cell transplantation – evidence for presence of disease-marker negative residual cells
title_short Automated detection of residual cells after sex-mismatched stem-cell transplantation – evidence for presence of disease-marker negative residual cells
title_sort automated detection of residual cells after sex-mismatched stem-cell transplantation – evidence for presence of disease-marker negative residual cells
topic Biochemistry (medical)
Genetics (clinical)
Genetics
Molecular Biology
Molecular Medicine
Biochemistry
url http://dx.doi.org/10.1186/1755-8166-2-12
publishDate 2009
physical
description <jats:title>Abstract</jats:title> <jats:sec> <jats:title>Background</jats:title> <jats:p>A new chimerism analysis based on automated interphase fluorescence in situ hybridization (FISH) evaluation was established to detect residual cells after allogene sex-mismatched bone marrow or blood stem-cell transplantation.</jats:p> <jats:p>Cells of 58 patients were characterized as disease-associated due to presence of a bcr/abl-gene-fusion or a trisomy 8 and/or a simultaneous hybridization of gonosome-specific centromeric probes. The automatic slide scanning platform Metafer with its module MetaCyte was used to analyse 3,000 cells per sample.</jats:p> </jats:sec> <jats:sec> <jats:title>Results</jats:title> <jats:p>Overall 454 assays of 58 patients were analyzed. 13 of 58 patients showed residual recipient cells at one stage of more than 4% and 12 of 58 showed residual recipient cells less than 4%, respectively. As to be expected, patients of the latter group were associated with a higher survival rate (48 vs. 34 month). In only two of seven patients with disease-marker positive residual cells between 0.1–1.3% a relapse was observed. Besides, disease-marker negative residual cells were found in two patients without relapse at a rate of 2.8% and 3.3%, respectively.</jats:p> </jats:sec> <jats:sec> <jats:title>Conclusion</jats:title> <jats:p>The definite origin and meaning of disease-marker negative residual cells is still unclear. Overall, with the presented automatic chimerism analysis of interphase FISH slides, a sensitive method for detection of disease-marker positive residual cells is on hand.</jats:p> </jats:sec>
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author Erlecke, Jörn, Hartmann, Isabell, Hoffmann, Martin, Kroll, Torsten, Starke, Heike, Heller, Anita, Gloria, Alexander, Sayer, Herbert G, Johannes, Tilman, Claussen, Uwe, Liehr, Thomas, Loncarevic, Ivan F
author_facet Erlecke, Jörn, Hartmann, Isabell, Hoffmann, Martin, Kroll, Torsten, Starke, Heike, Heller, Anita, Gloria, Alexander, Sayer, Herbert G, Johannes, Tilman, Claussen, Uwe, Liehr, Thomas, Loncarevic, Ivan F, Erlecke, Jörn, Hartmann, Isabell, Hoffmann, Martin, Kroll, Torsten, Starke, Heike, Heller, Anita, Gloria, Alexander, Sayer, Herbert G, Johannes, Tilman, Claussen, Uwe, Liehr, Thomas, Loncarevic, Ivan F
author_sort erlecke, jörn
container_issue 1
container_start_page 0
container_title Molecular Cytogenetics
container_volume 2
description <jats:title>Abstract</jats:title> <jats:sec> <jats:title>Background</jats:title> <jats:p>A new chimerism analysis based on automated interphase fluorescence in situ hybridization (FISH) evaluation was established to detect residual cells after allogene sex-mismatched bone marrow or blood stem-cell transplantation.</jats:p> <jats:p>Cells of 58 patients were characterized as disease-associated due to presence of a bcr/abl-gene-fusion or a trisomy 8 and/or a simultaneous hybridization of gonosome-specific centromeric probes. The automatic slide scanning platform Metafer with its module MetaCyte was used to analyse 3,000 cells per sample.</jats:p> </jats:sec> <jats:sec> <jats:title>Results</jats:title> <jats:p>Overall 454 assays of 58 patients were analyzed. 13 of 58 patients showed residual recipient cells at one stage of more than 4% and 12 of 58 showed residual recipient cells less than 4%, respectively. As to be expected, patients of the latter group were associated with a higher survival rate (48 vs. 34 month). In only two of seven patients with disease-marker positive residual cells between 0.1–1.3% a relapse was observed. Besides, disease-marker negative residual cells were found in two patients without relapse at a rate of 2.8% and 3.3%, respectively.</jats:p> </jats:sec> <jats:sec> <jats:title>Conclusion</jats:title> <jats:p>The definite origin and meaning of disease-marker negative residual cells is still unclear. Overall, with the presented automatic chimerism analysis of interphase FISH slides, a sensitive method for detection of disease-marker positive residual cells is on hand.</jats:p> </jats:sec>
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spelling Erlecke, Jörn Hartmann, Isabell Hoffmann, Martin Kroll, Torsten Starke, Heike Heller, Anita Gloria, Alexander Sayer, Herbert G Johannes, Tilman Claussen, Uwe Liehr, Thomas Loncarevic, Ivan F 1755-8166 Springer Science and Business Media LLC Biochemistry (medical) Genetics (clinical) Genetics Molecular Biology Molecular Medicine Biochemistry http://dx.doi.org/10.1186/1755-8166-2-12 <jats:title>Abstract</jats:title> <jats:sec> <jats:title>Background</jats:title> <jats:p>A new chimerism analysis based on automated interphase fluorescence in situ hybridization (FISH) evaluation was established to detect residual cells after allogene sex-mismatched bone marrow or blood stem-cell transplantation.</jats:p> <jats:p>Cells of 58 patients were characterized as disease-associated due to presence of a bcr/abl-gene-fusion or a trisomy 8 and/or a simultaneous hybridization of gonosome-specific centromeric probes. The automatic slide scanning platform Metafer with its module MetaCyte was used to analyse 3,000 cells per sample.</jats:p> </jats:sec> <jats:sec> <jats:title>Results</jats:title> <jats:p>Overall 454 assays of 58 patients were analyzed. 13 of 58 patients showed residual recipient cells at one stage of more than 4% and 12 of 58 showed residual recipient cells less than 4%, respectively. As to be expected, patients of the latter group were associated with a higher survival rate (48 vs. 34 month). In only two of seven patients with disease-marker positive residual cells between 0.1–1.3% a relapse was observed. Besides, disease-marker negative residual cells were found in two patients without relapse at a rate of 2.8% and 3.3%, respectively.</jats:p> </jats:sec> <jats:sec> <jats:title>Conclusion</jats:title> <jats:p>The definite origin and meaning of disease-marker negative residual cells is still unclear. Overall, with the presented automatic chimerism analysis of interphase FISH slides, a sensitive method for detection of disease-marker positive residual cells is on hand.</jats:p> </jats:sec> Automated detection of residual cells after sex-mismatched stem-cell transplantation – evidence for presence of disease-marker negative residual cells Molecular Cytogenetics
spellingShingle Erlecke, Jörn, Hartmann, Isabell, Hoffmann, Martin, Kroll, Torsten, Starke, Heike, Heller, Anita, Gloria, Alexander, Sayer, Herbert G, Johannes, Tilman, Claussen, Uwe, Liehr, Thomas, Loncarevic, Ivan F, Molecular Cytogenetics, Automated detection of residual cells after sex-mismatched stem-cell transplantation – evidence for presence of disease-marker negative residual cells, Biochemistry (medical), Genetics (clinical), Genetics, Molecular Biology, Molecular Medicine, Biochemistry
title Automated detection of residual cells after sex-mismatched stem-cell transplantation – evidence for presence of disease-marker negative residual cells
title_full Automated detection of residual cells after sex-mismatched stem-cell transplantation – evidence for presence of disease-marker negative residual cells
title_fullStr Automated detection of residual cells after sex-mismatched stem-cell transplantation – evidence for presence of disease-marker negative residual cells
title_full_unstemmed Automated detection of residual cells after sex-mismatched stem-cell transplantation – evidence for presence of disease-marker negative residual cells
title_short Automated detection of residual cells after sex-mismatched stem-cell transplantation – evidence for presence of disease-marker negative residual cells
title_sort automated detection of residual cells after sex-mismatched stem-cell transplantation – evidence for presence of disease-marker negative residual cells
title_unstemmed Automated detection of residual cells after sex-mismatched stem-cell transplantation – evidence for presence of disease-marker negative residual cells
topic Biochemistry (medical), Genetics (clinical), Genetics, Molecular Biology, Molecular Medicine, Biochemistry
url http://dx.doi.org/10.1186/1755-8166-2-12