Direct visualization of cytomegalovirus-specific T-cell reconstitution after allogeneic stem cell transplantation
Cytomegalovirus (CMV) remains an important cause of morbidity and mortality after allogeneic stem cell transplantation (SCT), but cytotoxic T lymphocytes (CTL) may play a critical role in controlling CMV reactivation. Fluorescent HLA-peptide tetramers containing immunodominant peptides from CMV were...
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Veröffentlicht in: | Blood 2001-03, Vol.97 (5), p.1232-1240 |
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description | Cytomegalovirus (CMV) remains an important cause of morbidity and mortality after allogeneic stem cell transplantation (SCT), but cytotoxic T lymphocytes (CTL) may play a critical role in controlling CMV reactivation. Fluorescent HLA-peptide tetramers containing immunodominant peptides from CMV were used to prospectively monitor the recovery of CMV CTL in recipients of allogeneic transplants from siblings (n = 13) or unrelated donors (n = 11). In patients given allografts from a sibling when both the patient and donor were seropositive for CMV before SCT, recovery of CMV-specific CTL was rapid and reached up to 21% of all CD8+ T cells. Early reconstitution of CMV-specific immunity was not observed if either the donor or recipient was seronegative for CMV. In recipients of transplants from volunteer unrelated donors, recovery of CMV-specific CTL was delayed in comparison to that in recipients of transplants from siblings and no CTL were observed within the first 100 days after SCT. CTL numbers were increased after episodes of CMV reactivation but were suppressed by prednisolone therapy. Recovery of CMV-specific CTL to levels greater than 10 × 106/L was associated with protection from CMV disease. It was concluded that use of HLA-peptide tetramers to quantify CMV CTL is valuable for studying T-cell responses after allogeneic SCT. It should allow prediction of CMV reactivation in individual patients and assist in the development of adoptive T-cell immunotherapy. |
doi_str_mv | 10.1182/blood.V97.5.1232 |
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Fluorescent HLA-peptide tetramers containing immunodominant peptides from CMV were used to prospectively monitor the recovery of CMV CTL in recipients of allogeneic transplants from siblings (n = 13) or unrelated donors (n = 11). In patients given allografts from a sibling when both the patient and donor were seropositive for CMV before SCT, recovery of CMV-specific CTL was rapid and reached up to 21% of all CD8+ T cells. Early reconstitution of CMV-specific immunity was not observed if either the donor or recipient was seronegative for CMV. In recipients of transplants from volunteer unrelated donors, recovery of CMV-specific CTL was delayed in comparison to that in recipients of transplants from siblings and no CTL were observed within the first 100 days after SCT. CTL numbers were increased after episodes of CMV reactivation but were suppressed by prednisolone therapy. Recovery of CMV-specific CTL to levels greater than 10 × 106/L was associated with protection from CMV disease. It was concluded that use of HLA-peptide tetramers to quantify CMV CTL is valuable for studying T-cell responses after allogeneic SCT. It should allow prediction of CMV reactivation in individual patients and assist in the development of adoptive T-cell immunotherapy.</description><identifier>ISSN: 0006-4971</identifier><identifier>EISSN: 1528-0020</identifier><identifier>DOI: 10.1182/blood.V97.5.1232</identifier><identifier>PMID: 11222365</identifier><language>eng</language><publisher>Washington, DC: Elsevier Inc</publisher><subject>Adolescent ; Adult ; Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy ; Anti-Inflammatory Agents - administration & dosage ; Antigens, Viral - blood ; Biological and medical sciences ; Bone marrow, stem cells transplantation. Graft versus host reaction ; Cohort Studies ; Cytomegalovirus - drug effects ; Cytomegalovirus - growth & development ; Cytomegalovirus - immunology ; Cytomegalovirus Infections - drug therapy ; Cytomegalovirus Infections - etiology ; Female ; Hematopoietic Stem Cell Transplantation - adverse effects ; Humans ; Lymphocyte Count ; Male ; Medical sciences ; Middle Aged ; Molecular Probes ; Phosphoproteins - blood ; Prednisolone - administration & dosage ; Prospective Studies ; T-Lymphocytes, Cytotoxic - cytology ; T-Lymphocytes, Cytotoxic - immunology ; T-Lymphocytes, Cytotoxic - virology ; Time Factors ; Transfusions. Complications. Transfusion reactions. Cell and gene therapy ; Transplantation, Homologous - adverse effects ; Viral Matrix Proteins - blood ; Virus Activation - immunology</subject><ispartof>Blood, 2001-03, Vol.97 (5), p.1232-1240</ispartof><rights>2001 American Society of Hematology</rights><rights>2001 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c464t-c394f7ea2c80108d170dc4a16e985ca0751726f493f782fac2860994b29b6c013</citedby><cites>FETCH-LOGICAL-c464t-c394f7ea2c80108d170dc4a16e985ca0751726f493f782fac2860994b29b6c013</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=1004966$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/11222365$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Cwynarski, Kate</creatorcontrib><creatorcontrib>Ainsworth, Jenni</creatorcontrib><creatorcontrib>Cobbold, Mark</creatorcontrib><creatorcontrib>Wagner, Simon</creatorcontrib><creatorcontrib>Mahendra, Prem</creatorcontrib><creatorcontrib>Apperley, Jane</creatorcontrib><creatorcontrib>Goldman, John</creatorcontrib><creatorcontrib>Craddock, Charles</creatorcontrib><creatorcontrib>Moss, Paul A.H.</creatorcontrib><title>Direct visualization of cytomegalovirus-specific T-cell reconstitution after allogeneic stem cell transplantation</title><title>Blood</title><addtitle>Blood</addtitle><description>Cytomegalovirus (CMV) remains an important cause of morbidity and mortality after allogeneic stem cell transplantation (SCT), but cytotoxic T lymphocytes (CTL) may play a critical role in controlling CMV reactivation. Fluorescent HLA-peptide tetramers containing immunodominant peptides from CMV were used to prospectively monitor the recovery of CMV CTL in recipients of allogeneic transplants from siblings (n = 13) or unrelated donors (n = 11). In patients given allografts from a sibling when both the patient and donor were seropositive for CMV before SCT, recovery of CMV-specific CTL was rapid and reached up to 21% of all CD8+ T cells. Early reconstitution of CMV-specific immunity was not observed if either the donor or recipient was seronegative for CMV. In recipients of transplants from volunteer unrelated donors, recovery of CMV-specific CTL was delayed in comparison to that in recipients of transplants from siblings and no CTL were observed within the first 100 days after SCT. CTL numbers were increased after episodes of CMV reactivation but were suppressed by prednisolone therapy. Recovery of CMV-specific CTL to levels greater than 10 × 106/L was associated with protection from CMV disease. It was concluded that use of HLA-peptide tetramers to quantify CMV CTL is valuable for studying T-cell responses after allogeneic SCT. It should allow prediction of CMV reactivation in individual patients and assist in the development of adoptive T-cell immunotherapy.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy</subject><subject>Anti-Inflammatory Agents - administration & dosage</subject><subject>Antigens, Viral - blood</subject><subject>Biological and medical sciences</subject><subject>Bone marrow, stem cells transplantation. Graft versus host reaction</subject><subject>Cohort Studies</subject><subject>Cytomegalovirus - drug effects</subject><subject>Cytomegalovirus - growth & development</subject><subject>Cytomegalovirus - immunology</subject><subject>Cytomegalovirus Infections - drug therapy</subject><subject>Cytomegalovirus Infections - etiology</subject><subject>Female</subject><subject>Hematopoietic Stem Cell Transplantation - adverse effects</subject><subject>Humans</subject><subject>Lymphocyte Count</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Molecular Probes</subject><subject>Phosphoproteins - blood</subject><subject>Prednisolone - administration & dosage</subject><subject>Prospective Studies</subject><subject>T-Lymphocytes, Cytotoxic - cytology</subject><subject>T-Lymphocytes, Cytotoxic - immunology</subject><subject>T-Lymphocytes, Cytotoxic - virology</subject><subject>Time Factors</subject><subject>Transfusions. Complications. Transfusion reactions. Cell and gene therapy</subject><subject>Transplantation, Homologous - adverse effects</subject><subject>Viral Matrix Proteins - blood</subject><subject>Virus Activation - immunology</subject><issn>0006-4971</issn><issn>1528-0020</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2001</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kUFv1DAQhS0EokvhzqnKAfWWZew4jt0b2paCVIlL4Wp5nXHlyom3trNS-fVksyuVS09z-d7T0zeEfKawplSyr9sQY7_-o7p1u6asYW_IirZM1gAM3pIVAIiaq46ekQ85PwJQ3rD2PTmjlDHWiHZFnq59Qluqvc-TCf6vKT6OVXSVfS5xwAcT4t6nKdd5h9Y7b6v72mII1ZyKYy6-TEvCuIKpMiHEBxxxxnLBoVrIksyYd8GMZSn_SN45EzJ-Ot1z8vv7zf3mR3336_bn5ttdbbngpbaN4q5Dw6wECrKnHfSWGypQydYa6FraMeG4alwnmTOWSQFK8S1TW2GBNufk8ti7S_Fpwlz04PNhkBkxTll3IFoq5QGEI2hTzDmh07vkB5OeNQV90KwXzXrWrFt90DxHLk7d03bA_iVw8joDX06AydYENyuwPv9XDFwJMWNXRwxnEXuPSWfrcbTYL1_RffSvj_gHTXydAA</recordid><startdate>20010301</startdate><enddate>20010301</enddate><creator>Cwynarski, Kate</creator><creator>Ainsworth, Jenni</creator><creator>Cobbold, Mark</creator><creator>Wagner, Simon</creator><creator>Mahendra, Prem</creator><creator>Apperley, Jane</creator><creator>Goldman, John</creator><creator>Craddock, Charles</creator><creator>Moss, Paul A.H.</creator><general>Elsevier Inc</general><general>The Americain Society of Hematology</general><scope>6I.</scope><scope>AAFTH</scope><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>20010301</creationdate><title>Direct visualization of cytomegalovirus-specific T-cell reconstitution after allogeneic stem cell transplantation</title><author>Cwynarski, Kate ; Ainsworth, Jenni ; Cobbold, Mark ; Wagner, Simon ; Mahendra, Prem ; Apperley, Jane ; Goldman, John ; Craddock, Charles ; Moss, Paul A.H.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c464t-c394f7ea2c80108d170dc4a16e985ca0751726f493f782fac2860994b29b6c013</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2001</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy</topic><topic>Anti-Inflammatory Agents - administration & dosage</topic><topic>Antigens, Viral - blood</topic><topic>Biological and medical sciences</topic><topic>Bone marrow, stem cells transplantation. Graft versus host reaction</topic><topic>Cohort Studies</topic><topic>Cytomegalovirus - drug effects</topic><topic>Cytomegalovirus - growth & development</topic><topic>Cytomegalovirus - immunology</topic><topic>Cytomegalovirus Infections - drug therapy</topic><topic>Cytomegalovirus Infections - etiology</topic><topic>Female</topic><topic>Hematopoietic Stem Cell Transplantation - adverse effects</topic><topic>Humans</topic><topic>Lymphocyte Count</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Molecular Probes</topic><topic>Phosphoproteins - blood</topic><topic>Prednisolone - administration & dosage</topic><topic>Prospective Studies</topic><topic>T-Lymphocytes, Cytotoxic - cytology</topic><topic>T-Lymphocytes, Cytotoxic - immunology</topic><topic>T-Lymphocytes, Cytotoxic - virology</topic><topic>Time Factors</topic><topic>Transfusions. Complications. Transfusion reactions. Cell and gene therapy</topic><topic>Transplantation, Homologous - adverse effects</topic><topic>Viral Matrix Proteins - blood</topic><topic>Virus Activation - immunology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Cwynarski, Kate</creatorcontrib><creatorcontrib>Ainsworth, Jenni</creatorcontrib><creatorcontrib>Cobbold, Mark</creatorcontrib><creatorcontrib>Wagner, Simon</creatorcontrib><creatorcontrib>Mahendra, Prem</creatorcontrib><creatorcontrib>Apperley, Jane</creatorcontrib><creatorcontrib>Goldman, John</creatorcontrib><creatorcontrib>Craddock, Charles</creatorcontrib><creatorcontrib>Moss, Paul A.H.</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><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>Blood</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Cwynarski, Kate</au><au>Ainsworth, Jenni</au><au>Cobbold, Mark</au><au>Wagner, Simon</au><au>Mahendra, Prem</au><au>Apperley, Jane</au><au>Goldman, John</au><au>Craddock, Charles</au><au>Moss, Paul A.H.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Direct visualization of cytomegalovirus-specific T-cell reconstitution after allogeneic stem cell transplantation</atitle><jtitle>Blood</jtitle><addtitle>Blood</addtitle><date>2001-03-01</date><risdate>2001</risdate><volume>97</volume><issue>5</issue><spage>1232</spage><epage>1240</epage><pages>1232-1240</pages><issn>0006-4971</issn><eissn>1528-0020</eissn><abstract>Cytomegalovirus (CMV) remains an important cause of morbidity and mortality after allogeneic stem cell transplantation (SCT), but cytotoxic T lymphocytes (CTL) may play a critical role in controlling CMV reactivation. Fluorescent HLA-peptide tetramers containing immunodominant peptides from CMV were used to prospectively monitor the recovery of CMV CTL in recipients of allogeneic transplants from siblings (n = 13) or unrelated donors (n = 11). In patients given allografts from a sibling when both the patient and donor were seropositive for CMV before SCT, recovery of CMV-specific CTL was rapid and reached up to 21% of all CD8+ T cells. Early reconstitution of CMV-specific immunity was not observed if either the donor or recipient was seronegative for CMV. In recipients of transplants from volunteer unrelated donors, recovery of CMV-specific CTL was delayed in comparison to that in recipients of transplants from siblings and no CTL were observed within the first 100 days after SCT. CTL numbers were increased after episodes of CMV reactivation but were suppressed by prednisolone therapy. Recovery of CMV-specific CTL to levels greater than 10 × 106/L was associated with protection from CMV disease. It was concluded that use of HLA-peptide tetramers to quantify CMV CTL is valuable for studying T-cell responses after allogeneic SCT. It should allow prediction of CMV reactivation in individual patients and assist in the development of adoptive T-cell immunotherapy.</abstract><cop>Washington, DC</cop><pub>Elsevier Inc</pub><pmid>11222365</pmid><doi>10.1182/blood.V97.5.1232</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adolescent Adult Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy Anti-Inflammatory Agents - administration & dosage Antigens, Viral - blood Biological and medical sciences Bone marrow, stem cells transplantation. Graft versus host reaction Cohort Studies Cytomegalovirus - drug effects Cytomegalovirus - growth & development Cytomegalovirus - immunology Cytomegalovirus Infections - drug therapy Cytomegalovirus Infections - etiology Female Hematopoietic Stem Cell Transplantation - adverse effects Humans Lymphocyte Count Male Medical sciences Middle Aged Molecular Probes Phosphoproteins - blood Prednisolone - administration & dosage Prospective Studies T-Lymphocytes, Cytotoxic - cytology T-Lymphocytes, Cytotoxic - immunology T-Lymphocytes, Cytotoxic - virology Time Factors Transfusions. Complications. Transfusion reactions. Cell and gene therapy Transplantation, Homologous - adverse effects Viral Matrix Proteins - blood Virus Activation - immunology |
title | Direct visualization of cytomegalovirus-specific T-cell reconstitution after allogeneic stem cell transplantation |
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