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Thymic recovery after allogeneic hematopoietic cell transplantation with non-myeloablative conditioning is limited to patients younger than 60 years of age
Long-term immune recovery in older patients given hematopoietic cell transplantation after non-myeloablative conditioning remains poorly understood. This prompted us to investigate long-term lymphocyte reconstitution and thymic function in 80 patients given allogeneic peripheral blood stem cells aft...
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Published in: | Haematologica (Roma) 2011-02, Vol.96 (2), p.298-306 |
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creator | CASTERMANS, Emilie HANNON, Muriel SANDMAIER, Brenda M STORB, Rainer BEGUIN, Yves BARON, Frédéric DUTRIEUX, Jacques HUMBLET-BARON, Stephanie SEIDEL, Laurence CHEYNIER, Remi WILLEMS, Evelyne GOTHOT, André VANBELLINGHEN, Jean-François GEENEN, Vincent |
description | Long-term immune recovery in older patients given hematopoietic cell transplantation after non-myeloablative conditioning remains poorly understood. This prompted us to investigate long-term lymphocyte reconstitution and thymic function in 80 patients given allogeneic peripheral blood stem cells after non-myeloablative conditioning.
Median age at transplant was 57 years (range 10-71). Conditioning regimen consisted of 2 Gy total body irradiation (TBI) with (n=46) or without (n=20) added fludarabine, 4 Gy TBI with fludarabine (n=6), or cyclophosphamide plus fludarabine (n=8). Stem cell sources were unmanipulated (n=56), CD8-depleted (n=19), or CD34-selected (n=5) peripheral blood stem cells. Immune recovery was assessed by signal-joint T-cell receptor excision circle quantification and flow cytometry.
Signal-joint T-cell receptor excision circle levels increased from day 100 to one and two years after transplantation in patients under 50 years of age (n=23; P=0.02 and P=0.04, respectively), and in those aged 51-60 years (n=35; P=0.17 and P=0.06, respectively), but not in patients aged over 60 (n=22; P=0.3 and P=0.3, respectively). Similarly, CD4(+)CD45RA(+) (naïve) T-cell counts increased from day 100 to one and two years after transplantation in patients aged 50 years and under 50 (P=0.002 and P=0.02, respectively), and in those aged 51-60 (P=0.4 and P=0.001, respectively), but less so in patients aged over 60 (P=0.3 and P=0.06, respectively). In multivariate analyses, older patient age (P |
doi_str_mv | 10.3324/haematol.2010.029702 |
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Median age at transplant was 57 years (range 10-71). Conditioning regimen consisted of 2 Gy total body irradiation (TBI) with (n=46) or without (n=20) added fludarabine, 4 Gy TBI with fludarabine (n=6), or cyclophosphamide plus fludarabine (n=8). Stem cell sources were unmanipulated (n=56), CD8-depleted (n=19), or CD34-selected (n=5) peripheral blood stem cells. Immune recovery was assessed by signal-joint T-cell receptor excision circle quantification and flow cytometry.
Signal-joint T-cell receptor excision circle levels increased from day 100 to one and two years after transplantation in patients under 50 years of age (n=23; P=0.02 and P=0.04, respectively), and in those aged 51-60 years (n=35; P=0.17 and P=0.06, respectively), but not in patients aged over 60 (n=22; P=0.3 and P=0.3, respectively). Similarly, CD4(+)CD45RA(+) (naïve) T-cell counts increased from day 100 to one and two years after transplantation in patients aged 50 years and under 50 (P=0.002 and P=0.02, respectively), and in those aged 51-60 (P=0.4 and P=0.001, respectively), but less so in patients aged over 60 (P=0.3 and P=0.06, respectively). In multivariate analyses, older patient age (P<0.001), extensive chronic GVHD (P<0.001), and prior (resolved) extensive chronic graft-versus-host disease (P=0.008) were associated with low signal-joint T-cell receptor excision circle levels one year or more after HCT.
In summary, our data suggest that thymic neo-generation of T cells occurred from day 100 onwards in patients under 60 while signal-joint T-cell receptor excision circle levels remained low for patients aged over 60. Further, chronic graft-versus-host disease had a dramatic impact on thymic function, as observed previously in patients given grafts after myeloablative conditioning.</description><identifier>ISSN: 0390-6078</identifier><identifier>EISSN: 1592-8721</identifier><identifier>DOI: 10.3324/haematol.2010.029702</identifier><identifier>PMID: 20934996</identifier><language>eng</language><publisher>Pavia: Ferrata Storti Foundation</publisher><subject>Adolescent ; Adult ; Aged ; Antineoplastic Combined Chemotherapy Protocols - therapeutic use ; Biological and medical sciences ; Child ; Chronic Disease ; Cyclophosphamide - administration & dosage ; Female ; Graft vs Host Disease - immunology ; Graft vs Host Disease - prevention & control ; Hematologic and hematopoietic diseases ; Hematopoietic Stem Cell Transplantation ; Humans ; Life Sciences ; Male ; Medical sciences ; Middle Aged ; Original ; Prognosis ; Receptors, Antigen, T-Cell - metabolism ; Survival Rate ; T-Lymphocytes - immunology ; T-Lymphocytes - metabolism ; Thymus Gland - immunology ; Thymus Gland - metabolism ; Transplantation Conditioning ; Transplantation, Homologous ; Vidarabine - administration & dosage ; Vidarabine - analogs & derivatives ; Whole-Body Irradiation ; Young Adult</subject><ispartof>Haematologica (Roma), 2011-02, Vol.96 (2), p.298-306</ispartof><rights>2015 INIST-CNRS</rights><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><rights>Copyright© Ferrata Storti Foundation</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c567t-759c52ffaf8f6d5e00eed411fd8add617b74b2e7262308e3cc8701776362dceb3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3031699/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3031699/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=24070744$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/20934996$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://hal.science/hal-04008253$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>CASTERMANS, Emilie</creatorcontrib><creatorcontrib>HANNON, Muriel</creatorcontrib><creatorcontrib>SANDMAIER, Brenda M</creatorcontrib><creatorcontrib>STORB, Rainer</creatorcontrib><creatorcontrib>BEGUIN, Yves</creatorcontrib><creatorcontrib>BARON, Frédéric</creatorcontrib><creatorcontrib>DUTRIEUX, Jacques</creatorcontrib><creatorcontrib>HUMBLET-BARON, Stephanie</creatorcontrib><creatorcontrib>SEIDEL, Laurence</creatorcontrib><creatorcontrib>CHEYNIER, Remi</creatorcontrib><creatorcontrib>WILLEMS, Evelyne</creatorcontrib><creatorcontrib>GOTHOT, André</creatorcontrib><creatorcontrib>VANBELLINGHEN, Jean-François</creatorcontrib><creatorcontrib>GEENEN, Vincent</creatorcontrib><title>Thymic recovery after allogeneic hematopoietic cell transplantation with non-myeloablative conditioning is limited to patients younger than 60 years of age</title><title>Haematologica (Roma)</title><addtitle>Haematologica</addtitle><description>Long-term immune recovery in older patients given hematopoietic cell transplantation after non-myeloablative conditioning remains poorly understood. This prompted us to investigate long-term lymphocyte reconstitution and thymic function in 80 patients given allogeneic peripheral blood stem cells after non-myeloablative conditioning.
Median age at transplant was 57 years (range 10-71). Conditioning regimen consisted of 2 Gy total body irradiation (TBI) with (n=46) or without (n=20) added fludarabine, 4 Gy TBI with fludarabine (n=6), or cyclophosphamide plus fludarabine (n=8). Stem cell sources were unmanipulated (n=56), CD8-depleted (n=19), or CD34-selected (n=5) peripheral blood stem cells. Immune recovery was assessed by signal-joint T-cell receptor excision circle quantification and flow cytometry.
Signal-joint T-cell receptor excision circle levels increased from day 100 to one and two years after transplantation in patients under 50 years of age (n=23; P=0.02 and P=0.04, respectively), and in those aged 51-60 years (n=35; P=0.17 and P=0.06, respectively), but not in patients aged over 60 (n=22; P=0.3 and P=0.3, respectively). Similarly, CD4(+)CD45RA(+) (naïve) T-cell counts increased from day 100 to one and two years after transplantation in patients aged 50 years and under 50 (P=0.002 and P=0.02, respectively), and in those aged 51-60 (P=0.4 and P=0.001, respectively), but less so in patients aged over 60 (P=0.3 and P=0.06, respectively). In multivariate analyses, older patient age (P<0.001), extensive chronic GVHD (P<0.001), and prior (resolved) extensive chronic graft-versus-host disease (P=0.008) were associated with low signal-joint T-cell receptor excision circle levels one year or more after HCT.
In summary, our data suggest that thymic neo-generation of T cells occurred from day 100 onwards in patients under 60 while signal-joint T-cell receptor excision circle levels remained low for patients aged over 60. Further, chronic graft-versus-host disease had a dramatic impact on thymic function, as observed previously in patients given grafts after myeloablative conditioning.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Aged</subject><subject>Antineoplastic Combined Chemotherapy Protocols - therapeutic use</subject><subject>Biological and medical sciences</subject><subject>Child</subject><subject>Chronic Disease</subject><subject>Cyclophosphamide - administration & dosage</subject><subject>Female</subject><subject>Graft vs Host Disease - immunology</subject><subject>Graft vs Host Disease - prevention & control</subject><subject>Hematologic and hematopoietic diseases</subject><subject>Hematopoietic Stem Cell Transplantation</subject><subject>Humans</subject><subject>Life Sciences</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Original</subject><subject>Prognosis</subject><subject>Receptors, Antigen, T-Cell - metabolism</subject><subject>Survival Rate</subject><subject>T-Lymphocytes - immunology</subject><subject>T-Lymphocytes - metabolism</subject><subject>Thymus Gland - immunology</subject><subject>Thymus Gland - metabolism</subject><subject>Transplantation Conditioning</subject><subject>Transplantation, Homologous</subject><subject>Vidarabine - administration & dosage</subject><subject>Vidarabine - analogs & derivatives</subject><subject>Whole-Body Irradiation</subject><subject>Young Adult</subject><issn>0390-6078</issn><issn>1592-8721</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>DOA</sourceid><recordid>eNpdks1u1DAUhSMEokPhDRDyhgWLFMdO7HiDVFVAK1ViU9aW41wnrhx7ZLszyrPwsng6_aGsLJ977nf9c6rqY4PPKCXt11nBonJwZwQXCRPBMXlVbZpOkLrnpHldbTAVuGaY9yfVu5RuMSZYCP62OikrbYVgm-rPzbwuVqMIOuwgrkiZDBEp58IEHkplvh-zDRZy2WlwDuWofNo65bPKNni0t3lGPvh6WcEFNbgi7wDp4Ed7MFg_IZuQs4vNMKIc0LY4wOeE1nDnpzIwz8ojhtEKKiYUDFITvK_eGOUSfHhYT6vfP77fXFzW179-Xl2cX9e6YzzXvBO6I8Yo0xs2doAxwNg2jRl7NY6s4QNvBwKcMEJxD1TrnuOGc0YZGTUM9LS6OnLHoG7lNtpFxVUGZeW9EOIkVSyXdyC5YaSl3GCheWt0pwYiVNFG0pcSg8L6dmRt74YFCt6Xx3IvoC8r3s5yCjtJMW2YEAXw5QiY_2u7PL-WBw23GPeko7umeNujV8eQUgTz1NBgeQiJfAyJPIREHkNS2j79e8anpsdUFMPnB4NKWjlTvlvb9OxrMce8bZ99s53mvY0g01KSU7BE7vd7wSSRRPT0L0kj2XI</recordid><startdate>20110201</startdate><enddate>20110201</enddate><creator>CASTERMANS, Emilie</creator><creator>HANNON, Muriel</creator><creator>SANDMAIER, Brenda M</creator><creator>STORB, Rainer</creator><creator>BEGUIN, Yves</creator><creator>BARON, Frédéric</creator><creator>DUTRIEUX, Jacques</creator><creator>HUMBLET-BARON, Stephanie</creator><creator>SEIDEL, Laurence</creator><creator>CHEYNIER, Remi</creator><creator>WILLEMS, Evelyne</creator><creator>GOTHOT, André</creator><creator>VANBELLINGHEN, Jean-François</creator><creator>GEENEN, Vincent</creator><general>Ferrata Storti Foundation</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>1XC</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20110201</creationdate><title>Thymic recovery after allogeneic hematopoietic cell transplantation with non-myeloablative conditioning is limited to patients younger than 60 years of age</title><author>CASTERMANS, Emilie ; HANNON, Muriel ; SANDMAIER, Brenda M ; STORB, Rainer ; BEGUIN, Yves ; BARON, Frédéric ; DUTRIEUX, Jacques ; HUMBLET-BARON, Stephanie ; SEIDEL, Laurence ; CHEYNIER, Remi ; WILLEMS, Evelyne ; GOTHOT, André ; VANBELLINGHEN, Jean-François ; GEENEN, Vincent</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c567t-759c52ffaf8f6d5e00eed411fd8add617b74b2e7262308e3cc8701776362dceb3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Aged</topic><topic>Antineoplastic Combined Chemotherapy Protocols - therapeutic use</topic><topic>Biological and medical sciences</topic><topic>Child</topic><topic>Chronic Disease</topic><topic>Cyclophosphamide - administration & dosage</topic><topic>Female</topic><topic>Graft vs Host Disease - immunology</topic><topic>Graft vs Host Disease - prevention & control</topic><topic>Hematologic and hematopoietic diseases</topic><topic>Hematopoietic Stem Cell Transplantation</topic><topic>Humans</topic><topic>Life Sciences</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Original</topic><topic>Prognosis</topic><topic>Receptors, Antigen, T-Cell - metabolism</topic><topic>Survival Rate</topic><topic>T-Lymphocytes - immunology</topic><topic>T-Lymphocytes - metabolism</topic><topic>Thymus Gland - immunology</topic><topic>Thymus Gland - metabolism</topic><topic>Transplantation Conditioning</topic><topic>Transplantation, Homologous</topic><topic>Vidarabine - administration & dosage</topic><topic>Vidarabine - analogs & derivatives</topic><topic>Whole-Body Irradiation</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>CASTERMANS, Emilie</creatorcontrib><creatorcontrib>HANNON, Muriel</creatorcontrib><creatorcontrib>SANDMAIER, Brenda M</creatorcontrib><creatorcontrib>STORB, Rainer</creatorcontrib><creatorcontrib>BEGUIN, Yves</creatorcontrib><creatorcontrib>BARON, Frédéric</creatorcontrib><creatorcontrib>DUTRIEUX, Jacques</creatorcontrib><creatorcontrib>HUMBLET-BARON, Stephanie</creatorcontrib><creatorcontrib>SEIDEL, Laurence</creatorcontrib><creatorcontrib>CHEYNIER, Remi</creatorcontrib><creatorcontrib>WILLEMS, Evelyne</creatorcontrib><creatorcontrib>GOTHOT, André</creatorcontrib><creatorcontrib>VANBELLINGHEN, Jean-François</creatorcontrib><creatorcontrib>GEENEN, Vincent</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>Hyper Article en Ligne (HAL)</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Haematologica (Roma)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>CASTERMANS, Emilie</au><au>HANNON, Muriel</au><au>SANDMAIER, Brenda M</au><au>STORB, Rainer</au><au>BEGUIN, Yves</au><au>BARON, Frédéric</au><au>DUTRIEUX, Jacques</au><au>HUMBLET-BARON, Stephanie</au><au>SEIDEL, Laurence</au><au>CHEYNIER, Remi</au><au>WILLEMS, Evelyne</au><au>GOTHOT, André</au><au>VANBELLINGHEN, Jean-François</au><au>GEENEN, Vincent</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Thymic recovery after allogeneic hematopoietic cell transplantation with non-myeloablative conditioning is limited to patients younger than 60 years of age</atitle><jtitle>Haematologica (Roma)</jtitle><addtitle>Haematologica</addtitle><date>2011-02-01</date><risdate>2011</risdate><volume>96</volume><issue>2</issue><spage>298</spage><epage>306</epage><pages>298-306</pages><issn>0390-6078</issn><eissn>1592-8721</eissn><abstract>Long-term immune recovery in older patients given hematopoietic cell transplantation after non-myeloablative conditioning remains poorly understood. This prompted us to investigate long-term lymphocyte reconstitution and thymic function in 80 patients given allogeneic peripheral blood stem cells after non-myeloablative conditioning.
Median age at transplant was 57 years (range 10-71). Conditioning regimen consisted of 2 Gy total body irradiation (TBI) with (n=46) or without (n=20) added fludarabine, 4 Gy TBI with fludarabine (n=6), or cyclophosphamide plus fludarabine (n=8). Stem cell sources were unmanipulated (n=56), CD8-depleted (n=19), or CD34-selected (n=5) peripheral blood stem cells. Immune recovery was assessed by signal-joint T-cell receptor excision circle quantification and flow cytometry.
Signal-joint T-cell receptor excision circle levels increased from day 100 to one and two years after transplantation in patients under 50 years of age (n=23; P=0.02 and P=0.04, respectively), and in those aged 51-60 years (n=35; P=0.17 and P=0.06, respectively), but not in patients aged over 60 (n=22; P=0.3 and P=0.3, respectively). Similarly, CD4(+)CD45RA(+) (naïve) T-cell counts increased from day 100 to one and two years after transplantation in patients aged 50 years and under 50 (P=0.002 and P=0.02, respectively), and in those aged 51-60 (P=0.4 and P=0.001, respectively), but less so in patients aged over 60 (P=0.3 and P=0.06, respectively). In multivariate analyses, older patient age (P<0.001), extensive chronic GVHD (P<0.001), and prior (resolved) extensive chronic graft-versus-host disease (P=0.008) were associated with low signal-joint T-cell receptor excision circle levels one year or more after HCT.
In summary, our data suggest that thymic neo-generation of T cells occurred from day 100 onwards in patients under 60 while signal-joint T-cell receptor excision circle levels remained low for patients aged over 60. Further, chronic graft-versus-host disease had a dramatic impact on thymic function, as observed previously in patients given grafts after myeloablative conditioning.</abstract><cop>Pavia</cop><pub>Ferrata Storti Foundation</pub><pmid>20934996</pmid><doi>10.3324/haematol.2010.029702</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adolescent Adult Aged Antineoplastic Combined Chemotherapy Protocols - therapeutic use Biological and medical sciences Child Chronic Disease Cyclophosphamide - administration & dosage Female Graft vs Host Disease - immunology Graft vs Host Disease - prevention & control Hematologic and hematopoietic diseases Hematopoietic Stem Cell Transplantation Humans Life Sciences Male Medical sciences Middle Aged Original Prognosis Receptors, Antigen, T-Cell - metabolism Survival Rate T-Lymphocytes - immunology T-Lymphocytes - metabolism Thymus Gland - immunology Thymus Gland - metabolism Transplantation Conditioning Transplantation, Homologous Vidarabine - administration & dosage Vidarabine - analogs & derivatives Whole-Body Irradiation Young Adult |
title | Thymic recovery after allogeneic hematopoietic cell transplantation with non-myeloablative conditioning is limited to patients younger than 60 years of age |
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