Clinical and immunologic outcomes following haplocompatible donor lymphocyte infusions
We retrospectively analyzed the characteristics of 16 consecutive pediatric patients who received one or more G-CSF-mobilized donor lymphocyte infusions (DLI) following a T-cell-depleted haplocompatible hematopoietic SCT (HSCT) to enhance immune recovery and/or treat an infection. The median time fr...
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Veröffentlicht in: | Bone marrow transplantation (Basingstoke) 2009-12, Vol.44 (12), p.805-812 |
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creator | Dvorak, C C Gilman, A L Horn, B Jaroscak, J Dunn, E A Baxter-Lowe, L A Cowan, M J |
description | We retrospectively analyzed the characteristics of 16 consecutive pediatric patients who received one or more G-CSF-mobilized donor lymphocyte infusions (DLI) following a T-cell-depleted haplocompatible hematopoietic SCT (HSCT) to enhance immune recovery and/or treat an infection. The median time from HSCT to administration of first DLI was 12 weeks and the median dose of DLI administered was 3 × 10
4
/kg (range, 2.5–6 × 10
4
/kg). The incidence of Grade I–II acute GVHD was 19% (95% confidence interval (CI), 6–44%), and there were no cases of Grade III–IV acute GVHD. Chronic GVHD developed in 13% (95% CI, 2–37%) of patients. In surviving patients who did not undergo a second stem cell infusion, T-cell numbers and function increased to a protective level in a median of 3 months (range, 2–12.5 months) following the first DLI administration. In patients given DLI for treatment of an infection, 75% (95% CI, 46–92%) cleared their infection after a median of 9 weeks (range, 1–27 weeks). In patients with CMV infection, the development of CMV-specific T cells was observed following DLI. The 1-year overall survival following haplocompatible DLI was 71% (95% CI, 59–83%), with a median follow-up of 16 months from the first DLI. |
doi_str_mv | 10.1038/bmt.2009.87 |
format | Article |
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4
/kg (range, 2.5–6 × 10
4
/kg). The incidence of Grade I–II acute GVHD was 19% (95% confidence interval (CI), 6–44%), and there were no cases of Grade III–IV acute GVHD. Chronic GVHD developed in 13% (95% CI, 2–37%) of patients. In surviving patients who did not undergo a second stem cell infusion, T-cell numbers and function increased to a protective level in a median of 3 months (range, 2–12.5 months) following the first DLI administration. In patients given DLI for treatment of an infection, 75% (95% CI, 46–92%) cleared their infection after a median of 9 weeks (range, 1–27 weeks). In patients with CMV infection, the development of CMV-specific T cells was observed following DLI. The 1-year overall survival following haplocompatible DLI was 71% (95% CI, 59–83%), with a median follow-up of 16 months from the first DLI.</description><identifier>ISSN: 0268-3369</identifier><identifier>EISSN: 1476-5365</identifier><identifier>DOI: 10.1038/bmt.2009.87</identifier><identifier>PMID: 19421175</identifier><identifier>CODEN: BMTRE9</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>Acute Disease ; Adolescent ; Adult ; Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy ; Biological and medical sciences ; Blood Donors ; Bone marrow, stem cells transplantation. Graft versus host reaction ; Cell Biology ; Child ; Child, Preschool ; Chronic Disease ; Confidence intervals ; Cytomegalovirus ; Cytomegalovirus - immunology ; Cytomegalovirus Infections - immunology ; Cytomegalovirus Infections - mortality ; Disease-Free Survival ; Female ; Graft vs Host Disease - blood ; Graft vs Host Disease - immunology ; Graft vs Host Disease - mortality ; Graft-versus-host reaction ; Granulocyte colony-stimulating factor ; Haplotypes ; Health aspects ; Hematologic Neoplasms - blood ; Hematologic Neoplasms - immunology ; Hematologic Neoplasms - mortality ; Hematologic Neoplasms - therapy ; Hematology ; Hematopoietic Stem Cell Transplantation ; Hematopoietic stem cells ; Humans ; Immune response ; Infant ; Infection ; Infections ; Internal Medicine ; Lymphocyte Transfusion ; Lymphocytes ; Lymphocytes T ; Male ; Medical sciences ; Medicine ; Medicine & Public Health ; original-article ; Patients ; Pediatrics ; Physiological aspects ; Prevention ; Public Health ; Recovery of Function - immunology ; Retrospective Studies ; Risk factors ; Severe Combined Immunodeficiency - blood ; Severe Combined Immunodeficiency - immunology ; Severe Combined Immunodeficiency - mortality ; Severe Combined Immunodeficiency - therapy ; Stem cell transplantation ; Stem Cells ; Survival Rate ; Time Factors ; Transfusions. Complications. Transfusion reactions. Cell and gene therapy ; Transplantation ; Transplantation, Homologous</subject><ispartof>Bone marrow transplantation (Basingstoke), 2009-12, Vol.44 (12), p.805-812</ispartof><rights>Macmillan Publishers Limited 2009</rights><rights>2015 INIST-CNRS</rights><rights>COPYRIGHT 2009 Nature Publishing Group</rights><rights>Copyright Nature Publishing Group Dec 2009</rights><rights>Macmillan Publishers Limited 2009.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c509t-3005099bc251ff66c2d2f8b0ad6f93f7d79ba06f87af2d24771dd4add9e802663</citedby><cites>FETCH-LOGICAL-c509t-3005099bc251ff66c2d2f8b0ad6f93f7d79ba06f87af2d24771dd4add9e802663</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1038/bmt.2009.87$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1038/bmt.2009.87$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,776,780,27901,27902,41464,42533,51294</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=22308376$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19421175$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Dvorak, C C</creatorcontrib><creatorcontrib>Gilman, A L</creatorcontrib><creatorcontrib>Horn, B</creatorcontrib><creatorcontrib>Jaroscak, J</creatorcontrib><creatorcontrib>Dunn, E A</creatorcontrib><creatorcontrib>Baxter-Lowe, L A</creatorcontrib><creatorcontrib>Cowan, M J</creatorcontrib><title>Clinical and immunologic outcomes following haplocompatible donor lymphocyte infusions</title><title>Bone marrow transplantation (Basingstoke)</title><addtitle>Bone Marrow Transplant</addtitle><addtitle>Bone Marrow Transplant</addtitle><description>We retrospectively analyzed the characteristics of 16 consecutive pediatric patients who received one or more G-CSF-mobilized donor lymphocyte infusions (DLI) following a T-cell-depleted haplocompatible hematopoietic SCT (HSCT) to enhance immune recovery and/or treat an infection. The median time from HSCT to administration of first DLI was 12 weeks and the median dose of DLI administered was 3 × 10
4
/kg (range, 2.5–6 × 10
4
/kg). The incidence of Grade I–II acute GVHD was 19% (95% confidence interval (CI), 6–44%), and there were no cases of Grade III–IV acute GVHD. Chronic GVHD developed in 13% (95% CI, 2–37%) of patients. In surviving patients who did not undergo a second stem cell infusion, T-cell numbers and function increased to a protective level in a median of 3 months (range, 2–12.5 months) following the first DLI administration. In patients given DLI for treatment of an infection, 75% (95% CI, 46–92%) cleared their infection after a median of 9 weeks (range, 1–27 weeks). In patients with CMV infection, the development of CMV-specific T cells was observed following DLI. The 1-year overall survival following haplocompatible DLI was 71% (95% CI, 59–83%), with a median follow-up of 16 months from the first DLI.</description><subject>Acute Disease</subject><subject>Adolescent</subject><subject>Adult</subject><subject>Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy</subject><subject>Biological and medical sciences</subject><subject>Blood Donors</subject><subject>Bone marrow, stem cells transplantation. Graft versus host reaction</subject><subject>Cell Biology</subject><subject>Child</subject><subject>Child, Preschool</subject><subject>Chronic Disease</subject><subject>Confidence intervals</subject><subject>Cytomegalovirus</subject><subject>Cytomegalovirus - immunology</subject><subject>Cytomegalovirus Infections - immunology</subject><subject>Cytomegalovirus Infections - mortality</subject><subject>Disease-Free Survival</subject><subject>Female</subject><subject>Graft vs Host Disease - blood</subject><subject>Graft vs Host Disease - immunology</subject><subject>Graft vs Host Disease - mortality</subject><subject>Graft-versus-host reaction</subject><subject>Granulocyte colony-stimulating factor</subject><subject>Haplotypes</subject><subject>Health aspects</subject><subject>Hematologic Neoplasms - blood</subject><subject>Hematologic Neoplasms - immunology</subject><subject>Hematologic Neoplasms - mortality</subject><subject>Hematologic Neoplasms - therapy</subject><subject>Hematology</subject><subject>Hematopoietic Stem Cell Transplantation</subject><subject>Hematopoietic stem cells</subject><subject>Humans</subject><subject>Immune response</subject><subject>Infant</subject><subject>Infection</subject><subject>Infections</subject><subject>Internal Medicine</subject><subject>Lymphocyte Transfusion</subject><subject>Lymphocytes</subject><subject>Lymphocytes T</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>original-article</subject><subject>Patients</subject><subject>Pediatrics</subject><subject>Physiological aspects</subject><subject>Prevention</subject><subject>Public Health</subject><subject>Recovery of Function - immunology</subject><subject>Retrospective Studies</subject><subject>Risk factors</subject><subject>Severe Combined Immunodeficiency - blood</subject><subject>Severe Combined Immunodeficiency - immunology</subject><subject>Severe Combined Immunodeficiency - mortality</subject><subject>Severe Combined Immunodeficiency - therapy</subject><subject>Stem cell transplantation</subject><subject>Stem Cells</subject><subject>Survival Rate</subject><subject>Time Factors</subject><subject>Transfusions. Complications. Transfusion reactions. Cell and gene therapy</subject><subject>Transplantation</subject><subject>Transplantation, Homologous</subject><issn>0268-3369</issn><issn>1476-5365</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNp90cur1DAUB-Agine8unIvRVEX2jGPNo_lZfAFF9yo25DmMZNLmtSkRea_N2UGB0RdBXI-zsnJD4CnCG4RJPzdMM5bDKHYcnYPbFDHaNsT2t8HG4gpbwmh4go8KuUOQtR1sH8IrpDoMEKs34Dvu-Cj1yo0KprGj-MSU0h7r5u0zDqNtjQuhZB--rhvDmoKqV5OavZDsI1JMeUmHMfpkPRxto2Pbik-xfIYPHAqFPvkfF6Dbx_ef919am-_fPy8u7ltdQ_F3BII6ykGjXvkHKUaG-z4AJWhThDHDBODgtRxplwtdYwhYzpljLC8LkfJNXh96jvl9GOxZZajL9qGoKJNS5GMdBj2nMIqX_1XYkQIFpxU-OIPeJeWHOsWEtMOY8g5F1U9_6dClFKIBL3M3Ktg5cGqMB9KCsu8fpG8wajna0NW4ZsT1DmVkq2TU_ajykeJoFxDljVkuYYs-aqfnWcvw2jNxZ5TreDlGahSo3VZRe3Lb4cxgZyw9X1vT67UUtzbfFnib3N_ASbAvQM</recordid><startdate>20091201</startdate><enddate>20091201</enddate><creator>Dvorak, C C</creator><creator>Gilman, A L</creator><creator>Horn, B</creator><creator>Jaroscak, J</creator><creator>Dunn, E A</creator><creator>Baxter-Lowe, L A</creator><creator>Cowan, M J</creator><general>Nature Publishing Group UK</general><general>Nature Publishing Group</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>3V.</scope><scope>7QO</scope><scope>7QP</scope><scope>7T5</scope><scope>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>M7P</scope><scope>P64</scope><scope>PHGZM</scope><scope>PHGZT</scope><scope>PJZUB</scope><scope>PKEHL</scope><scope>PPXIY</scope><scope>PQEST</scope><scope>PQGLB</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope></search><sort><creationdate>20091201</creationdate><title>Clinical and immunologic outcomes following haplocompatible donor lymphocyte infusions</title><author>Dvorak, C C ; Gilman, A L ; Horn, B ; Jaroscak, J ; Dunn, E A ; Baxter-Lowe, L A ; Cowan, M J</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c509t-3005099bc251ff66c2d2f8b0ad6f93f7d79ba06f87af2d24771dd4add9e802663</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Acute Disease</topic><topic>Adolescent</topic><topic>Adult</topic><topic>Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy</topic><topic>Biological and medical sciences</topic><topic>Blood Donors</topic><topic>Bone marrow, stem cells transplantation. Graft versus host reaction</topic><topic>Cell Biology</topic><topic>Child</topic><topic>Child, Preschool</topic><topic>Chronic Disease</topic><topic>Confidence intervals</topic><topic>Cytomegalovirus</topic><topic>Cytomegalovirus - immunology</topic><topic>Cytomegalovirus Infections - immunology</topic><topic>Cytomegalovirus Infections - mortality</topic><topic>Disease-Free Survival</topic><topic>Female</topic><topic>Graft vs Host Disease - blood</topic><topic>Graft vs Host Disease - immunology</topic><topic>Graft vs Host Disease - mortality</topic><topic>Graft-versus-host reaction</topic><topic>Granulocyte colony-stimulating factor</topic><topic>Haplotypes</topic><topic>Health aspects</topic><topic>Hematologic Neoplasms - blood</topic><topic>Hematologic Neoplasms - immunology</topic><topic>Hematologic Neoplasms - mortality</topic><topic>Hematologic Neoplasms - therapy</topic><topic>Hematology</topic><topic>Hematopoietic Stem Cell Transplantation</topic><topic>Hematopoietic stem cells</topic><topic>Humans</topic><topic>Immune response</topic><topic>Infant</topic><topic>Infection</topic><topic>Infections</topic><topic>Internal Medicine</topic><topic>Lymphocyte Transfusion</topic><topic>Lymphocytes</topic><topic>Lymphocytes T</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>original-article</topic><topic>Patients</topic><topic>Pediatrics</topic><topic>Physiological aspects</topic><topic>Prevention</topic><topic>Public Health</topic><topic>Recovery of Function - immunology</topic><topic>Retrospective Studies</topic><topic>Risk factors</topic><topic>Severe Combined Immunodeficiency - blood</topic><topic>Severe Combined Immunodeficiency - immunology</topic><topic>Severe Combined Immunodeficiency - mortality</topic><topic>Severe Combined Immunodeficiency - therapy</topic><topic>Stem cell transplantation</topic><topic>Stem Cells</topic><topic>Survival Rate</topic><topic>Time Factors</topic><topic>Transfusions. Complications. Transfusion reactions. Cell and gene therapy</topic><topic>Transplantation</topic><topic>Transplantation, Homologous</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Dvorak, C C</creatorcontrib><creatorcontrib>Gilman, A L</creatorcontrib><creatorcontrib>Horn, B</creatorcontrib><creatorcontrib>Jaroscak, J</creatorcontrib><creatorcontrib>Dunn, E A</creatorcontrib><creatorcontrib>Baxter-Lowe, L A</creatorcontrib><creatorcontrib>Cowan, M 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>ProQuest Central (Corporate)</collection><collection>Biotechnology Research Abstracts</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Immunology Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biological Science Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>ProQuest Central (New)</collection><collection>ProQuest One Academic (New)</collection><collection>ProQuest Health & Medical Research Collection</collection><collection>ProQuest One Academic Middle East (New)</collection><collection>ProQuest One Health & Nursing</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Applied & Life Sciences</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><jtitle>Bone marrow transplantation (Basingstoke)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Dvorak, C C</au><au>Gilman, A L</au><au>Horn, B</au><au>Jaroscak, J</au><au>Dunn, E A</au><au>Baxter-Lowe, L A</au><au>Cowan, M J</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Clinical and immunologic outcomes following haplocompatible donor lymphocyte infusions</atitle><jtitle>Bone marrow transplantation (Basingstoke)</jtitle><stitle>Bone Marrow Transplant</stitle><addtitle>Bone Marrow Transplant</addtitle><date>2009-12-01</date><risdate>2009</risdate><volume>44</volume><issue>12</issue><spage>805</spage><epage>812</epage><pages>805-812</pages><issn>0268-3369</issn><eissn>1476-5365</eissn><coden>BMTRE9</coden><abstract>We retrospectively analyzed the characteristics of 16 consecutive pediatric patients who received one or more G-CSF-mobilized donor lymphocyte infusions (DLI) following a T-cell-depleted haplocompatible hematopoietic SCT (HSCT) to enhance immune recovery and/or treat an infection. The median time from HSCT to administration of first DLI was 12 weeks and the median dose of DLI administered was 3 × 10
4
/kg (range, 2.5–6 × 10
4
/kg). The incidence of Grade I–II acute GVHD was 19% (95% confidence interval (CI), 6–44%), and there were no cases of Grade III–IV acute GVHD. Chronic GVHD developed in 13% (95% CI, 2–37%) of patients. In surviving patients who did not undergo a second stem cell infusion, T-cell numbers and function increased to a protective level in a median of 3 months (range, 2–12.5 months) following the first DLI administration. In patients given DLI for treatment of an infection, 75% (95% CI, 46–92%) cleared their infection after a median of 9 weeks (range, 1–27 weeks). In patients with CMV infection, the development of CMV-specific T cells was observed following DLI. The 1-year overall survival following haplocompatible DLI was 71% (95% CI, 59–83%), with a median follow-up of 16 months from the first DLI.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>19421175</pmid><doi>10.1038/bmt.2009.87</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Acute Disease Adolescent Adult Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy Biological and medical sciences Blood Donors Bone marrow, stem cells transplantation. Graft versus host reaction Cell Biology Child Child, Preschool Chronic Disease Confidence intervals Cytomegalovirus Cytomegalovirus - immunology Cytomegalovirus Infections - immunology Cytomegalovirus Infections - mortality Disease-Free Survival Female Graft vs Host Disease - blood Graft vs Host Disease - immunology Graft vs Host Disease - mortality Graft-versus-host reaction Granulocyte colony-stimulating factor Haplotypes Health aspects Hematologic Neoplasms - blood Hematologic Neoplasms - immunology Hematologic Neoplasms - mortality Hematologic Neoplasms - therapy Hematology Hematopoietic Stem Cell Transplantation Hematopoietic stem cells Humans Immune response Infant Infection Infections Internal Medicine Lymphocyte Transfusion Lymphocytes Lymphocytes T Male Medical sciences Medicine Medicine & Public Health original-article Patients Pediatrics Physiological aspects Prevention Public Health Recovery of Function - immunology Retrospective Studies Risk factors Severe Combined Immunodeficiency - blood Severe Combined Immunodeficiency - immunology Severe Combined Immunodeficiency - mortality Severe Combined Immunodeficiency - therapy Stem cell transplantation Stem Cells Survival Rate Time Factors Transfusions. Complications. Transfusion reactions. Cell and gene therapy Transplantation Transplantation, Homologous |
title | Clinical and immunologic outcomes following haplocompatible donor lymphocyte infusions |
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