Detection of chimerism and early engraftment after allogeneic peripheral blood stem cell or bone marrow transplantation by short tandem repeats

Chimerism can be monitored after HLA‐matched allogeneic bone marrow transplantation (BMT) or allogeneic peripheral blood stem cell transplantation (PBSCT) by detecting polymorphisms in short tandem repeats (STR). The purpose of our study was to document early complete chimerism in BMT and PBSCT reci...

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Veröffentlicht in:American journal of hematology 1996-08, Vol.52 (4), p.281-287
Hauptverfasser: Frankel, W., Chan, A., Corringham, R.E. T., Shepherd, S., Rearden, A., Wang‐Rodriguez, J.
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container_end_page 287
container_issue 4
container_start_page 281
container_title American journal of hematology
container_volume 52
creator Frankel, W.
Chan, A.
Corringham, R.E. T.
Shepherd, S.
Rearden, A.
Wang‐Rodriguez, J.
description Chimerism can be monitored after HLA‐matched allogeneic bone marrow transplantation (BMT) or allogeneic peripheral blood stem cell transplantation (PBSCT) by detecting polymorphisms in short tandem repeats (STR). The purpose of our study was to document early complete chimerism in BMT and PBSCT recipients using STR, and to determine whether the initial WBC recovery correlated with the days required to attain complete chimerism. A total of 5 patients (2 PBSCT and 3 BMT) were followed by STR after transplantation. Peripheral blood obtained prior to transplantation was used to determine the 2 most informative STR probes for each donor/recipient pair. STR were amplified by polymerase chain reaction (PCR) with 8 commercial probes, and PCR products were visualized with silver staining. Peripheral blood was evaluated daily post‐transplantation for WBC counts and to identify the presence of mixed or full chimerism by STR. The sensitivity of the STR technique varied from 0.05 to 1%, depending on the probe. Full chimerism was documented between day 9 and 14 in PBSCT recipients and on day 14 and 16 in BMT recipients. The initial rise in WBC occurred within 3 days of the onset of full chimerism, indicating that full chimerism is a more sensitive indicator of early engraftment. Periodic recipient monitoring using STR after complete chimerism identifies those patients who revert to mixed chimeras. The STR method may be useful in future studies to determine the significance of early engraftment and the clinical implications of sustained complete chimerism or mixed chimerism. © 1996 Wiley‐Liss, Inc.
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T. ; Shepherd, S. ; Rearden, A. ; Wang‐Rodriguez, J.</creator><creatorcontrib>Frankel, W. ; Chan, A. ; Corringham, R.E. T. ; Shepherd, S. ; Rearden, A. ; Wang‐Rodriguez, J.</creatorcontrib><description>Chimerism can be monitored after HLA‐matched allogeneic bone marrow transplantation (BMT) or allogeneic peripheral blood stem cell transplantation (PBSCT) by detecting polymorphisms in short tandem repeats (STR). The purpose of our study was to document early complete chimerism in BMT and PBSCT recipients using STR, and to determine whether the initial WBC recovery correlated with the days required to attain complete chimerism. A total of 5 patients (2 PBSCT and 3 BMT) were followed by STR after transplantation. Peripheral blood obtained prior to transplantation was used to determine the 2 most informative STR probes for each donor/recipient pair. STR were amplified by polymerase chain reaction (PCR) with 8 commercial probes, and PCR products were visualized with silver staining. 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Graft versus host reaction ; chimerism ; DNA - analysis ; DNA Probes ; Graft vs Host Disease ; Hematopoietic Stem Cell Transplantation ; HLA ; Humans ; Leukemia, Myeloid, Acute - therapy ; Leukocyte Count ; Lymphoma, Non-Hodgkin - therapy ; Medical sciences ; Middle Aged ; Multiple Myeloma - therapy ; Polymerase Chain Reaction ; Precursor Cell Lymphoblastic Leukemia-Lymphoma - therapy ; Repetitive Sequences, Nucleic Acid ; short tandem repeats ; Silver Staining ; Transfusions. Complications. Transfusion reactions. 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T.</creatorcontrib><creatorcontrib>Shepherd, S.</creatorcontrib><creatorcontrib>Rearden, A.</creatorcontrib><creatorcontrib>Wang‐Rodriguez, J.</creatorcontrib><title>Detection of chimerism and early engraftment after allogeneic peripheral blood stem cell or bone marrow transplantation by short tandem repeats</title><title>American journal of hematology</title><addtitle>Am J Hematol</addtitle><description>Chimerism can be monitored after HLA‐matched allogeneic bone marrow transplantation (BMT) or allogeneic peripheral blood stem cell transplantation (PBSCT) by detecting polymorphisms in short tandem repeats (STR). The purpose of our study was to document early complete chimerism in BMT and PBSCT recipients using STR, and to determine whether the initial WBC recovery correlated with the days required to attain complete chimerism. A total of 5 patients (2 PBSCT and 3 BMT) were followed by STR after transplantation. Peripheral blood obtained prior to transplantation was used to determine the 2 most informative STR probes for each donor/recipient pair. STR were amplified by polymerase chain reaction (PCR) with 8 commercial probes, and PCR products were visualized with silver staining. Peripheral blood was evaluated daily post‐transplantation for WBC counts and to identify the presence of mixed or full chimerism by STR. The sensitivity of the STR technique varied from 0.05 to 1%, depending on the probe. Full chimerism was documented between day 9 and 14 in PBSCT recipients and on day 14 and 16 in BMT recipients. The initial rise in WBC occurred within 3 days of the onset of full chimerism, indicating that full chimerism is a more sensitive indicator of early engraftment. Periodic recipient monitoring using STR after complete chimerism identifies those patients who revert to mixed chimeras. The STR method may be useful in future studies to determine the significance of early engraftment and the clinical implications of sustained complete chimerism or mixed chimerism. © 1996 Wiley‐Liss, Inc.</description><subject>Adult</subject><subject>allogeneic bone marrow transplantation</subject><subject>Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy</subject><subject>Biological and medical sciences</subject><subject>Bone Marrow Transplantation</subject><subject>Bone marrow, stem cells transplantation. Graft versus host reaction</subject><subject>chimerism</subject><subject>DNA - analysis</subject><subject>DNA Probes</subject><subject>Graft vs Host Disease</subject><subject>Hematopoietic Stem Cell Transplantation</subject><subject>HLA</subject><subject>Humans</subject><subject>Leukemia, Myeloid, Acute - therapy</subject><subject>Leukocyte Count</subject><subject>Lymphoma, Non-Hodgkin - therapy</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Multiple Myeloma - therapy</subject><subject>Polymerase Chain Reaction</subject><subject>Precursor Cell Lymphoblastic Leukemia-Lymphoma - therapy</subject><subject>Repetitive Sequences, Nucleic Acid</subject><subject>short tandem repeats</subject><subject>Silver Staining</subject><subject>Transfusions. Complications. Transfusion reactions. 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T.</creator><creator>Shepherd, S.</creator><creator>Rearden, A.</creator><creator>Wang‐Rodriguez, J.</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><general>Wiley-Liss</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>199608</creationdate><title>Detection of chimerism and early engraftment after allogeneic peripheral blood stem cell or bone marrow transplantation by short tandem repeats</title><author>Frankel, W. ; Chan, A. ; Corringham, R.E. T. ; Shepherd, S. ; Rearden, A. ; Wang‐Rodriguez, J.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5317-47b56916e5815798b6900d75171056015c8fcf99a6357077005331cf71b651c73</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1996</creationdate><topic>Adult</topic><topic>allogeneic bone marrow transplantation</topic><topic>Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy</topic><topic>Biological and medical sciences</topic><topic>Bone Marrow Transplantation</topic><topic>Bone marrow, stem cells transplantation. Graft versus host reaction</topic><topic>chimerism</topic><topic>DNA - analysis</topic><topic>DNA Probes</topic><topic>Graft vs Host Disease</topic><topic>Hematopoietic Stem Cell Transplantation</topic><topic>HLA</topic><topic>Humans</topic><topic>Leukemia, Myeloid, Acute - therapy</topic><topic>Leukocyte Count</topic><topic>Lymphoma, Non-Hodgkin - therapy</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Multiple Myeloma - therapy</topic><topic>Polymerase Chain Reaction</topic><topic>Precursor Cell Lymphoblastic Leukemia-Lymphoma - therapy</topic><topic>Repetitive Sequences, Nucleic Acid</topic><topic>short tandem repeats</topic><topic>Silver Staining</topic><topic>Transfusions. Complications. Transfusion reactions. Cell and gene therapy</topic><topic>Transplantation Chimera</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Frankel, W.</creatorcontrib><creatorcontrib>Chan, A.</creatorcontrib><creatorcontrib>Corringham, R.E. T.</creatorcontrib><creatorcontrib>Shepherd, S.</creatorcontrib><creatorcontrib>Rearden, A.</creatorcontrib><creatorcontrib>Wang‐Rodriguez, J.</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>American journal of hematology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Frankel, W.</au><au>Chan, A.</au><au>Corringham, R.E. T.</au><au>Shepherd, S.</au><au>Rearden, A.</au><au>Wang‐Rodriguez, J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Detection of chimerism and early engraftment after allogeneic peripheral blood stem cell or bone marrow transplantation by short tandem repeats</atitle><jtitle>American journal of hematology</jtitle><addtitle>Am J Hematol</addtitle><date>1996-08</date><risdate>1996</risdate><volume>52</volume><issue>4</issue><spage>281</spage><epage>287</epage><pages>281-287</pages><issn>0361-8609</issn><eissn>1096-8652</eissn><coden>AJHEDD</coden><abstract>Chimerism can be monitored after HLA‐matched allogeneic bone marrow transplantation (BMT) or allogeneic peripheral blood stem cell transplantation (PBSCT) by detecting polymorphisms in short tandem repeats (STR). The purpose of our study was to document early complete chimerism in BMT and PBSCT recipients using STR, and to determine whether the initial WBC recovery correlated with the days required to attain complete chimerism. A total of 5 patients (2 PBSCT and 3 BMT) were followed by STR after transplantation. Peripheral blood obtained prior to transplantation was used to determine the 2 most informative STR probes for each donor/recipient pair. STR were amplified by polymerase chain reaction (PCR) with 8 commercial probes, and PCR products were visualized with silver staining. Peripheral blood was evaluated daily post‐transplantation for WBC counts and to identify the presence of mixed or full chimerism by STR. The sensitivity of the STR technique varied from 0.05 to 1%, depending on the probe. Full chimerism was documented between day 9 and 14 in PBSCT recipients and on day 14 and 16 in BMT recipients. The initial rise in WBC occurred within 3 days of the onset of full chimerism, indicating that full chimerism is a more sensitive indicator of early engraftment. Periodic recipient monitoring using STR after complete chimerism identifies those patients who revert to mixed chimeras. The STR method may be useful in future studies to determine the significance of early engraftment and the clinical implications of sustained complete chimerism or mixed chimerism. © 1996 Wiley‐Liss, Inc.</abstract><cop>New York</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>8701946</pmid><doi>10.1002/(SICI)1096-8652(199608)52:4&lt;281::AID-AJH7&gt;3.0.CO;2-O</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record>
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subjects Adult
allogeneic bone marrow transplantation
Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy
Biological and medical sciences
Bone Marrow Transplantation
Bone marrow, stem cells transplantation. Graft versus host reaction
chimerism
DNA - analysis
DNA Probes
Graft vs Host Disease
Hematopoietic Stem Cell Transplantation
HLA
Humans
Leukemia, Myeloid, Acute - therapy
Leukocyte Count
Lymphoma, Non-Hodgkin - therapy
Medical sciences
Middle Aged
Multiple Myeloma - therapy
Polymerase Chain Reaction
Precursor Cell Lymphoblastic Leukemia-Lymphoma - therapy
Repetitive Sequences, Nucleic Acid
short tandem repeats
Silver Staining
Transfusions. Complications. Transfusion reactions. Cell and gene therapy
Transplantation Chimera
title Detection of chimerism and early engraftment after allogeneic peripheral blood stem cell or bone marrow transplantation by short tandem repeats
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