Generation of functional CLL-specific cord blood CTL using CD40-ligated CLL APC

Though remissions have been observed following allo-HSCT for the treatment of CLL, many CLL patients are ineligible for transplant due to the lack of HLA-compatible donors. The use of umbilical cord blood (UCB) permits transplantation of many patients who lack HLA-compatible donors due to reduced re...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:PloS one 2012-12, Vol.7 (12), p.e51390-e51390
Hauptverfasser: Decker, William K, Shah, Nina, Xing, Dongxia, Lapushin, Ruth, Li, Sufang, Robinson, Simon N, Yang, Hong, Parmar, Simrit, Halpert, Matthew M, Keating, Michael J, Gribben, John G, Molldrem, Jeffrey J, Shpall, Elizabeth J, Wierda, William G
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page e51390
container_issue 12
container_start_page e51390
container_title PloS one
container_volume 7
creator Decker, William K
Shah, Nina
Xing, Dongxia
Lapushin, Ruth
Li, Sufang
Robinson, Simon N
Yang, Hong
Parmar, Simrit
Halpert, Matthew M
Keating, Michael J
Gribben, John G
Molldrem, Jeffrey J
Shpall, Elizabeth J
Wierda, William G
description Though remissions have been observed following allo-HSCT for the treatment of CLL, many CLL patients are ineligible for transplant due to the lack of HLA-compatible donors. The use of umbilical cord blood (UCB) permits transplantation of many patients who lack HLA-compatible donors due to reduced requirements for stringent HLA matching between graft and recipient; however, disease relapse remains a concern with this modality. The generation of CLL-specific CTL from UCB T-cells, primed and expanded against the leukemic clone, might enhance the GVL effect and improve outcomes with UCB transplantation. Here we report the generation of functional, CLL-specific CTL using CD40-ligated CLL cells to prime partially-HLA matched UCB T-cells. Functionality and specificity were demonstrated by immune synapse assay, IFN-γ ELISpot, multi-parametric intracellular cytokine flow cytometry, and (51)Cr release assay. The use of patient-specific, non-CLL controls demonstrated the generation of both alloantigen and CLL-specific responses. Subsequently, we developed a clinically-applicable procedure permitting separation of alloreactive CTL from leukemia-specific CTL. Leukemia-specific CTL were able to mediate in vivo killing of CLL in humanized mice without concurrent or subsequent development of xenoGVHD. Our results demonstrate that generation of CLL-specific effectors from UCB is feasible and practical, and the results support further exploration of this strategy as a treatment modality for CLL.
doi_str_mv 10.1371/journal.pone.0051390
format Article
fullrecord <record><control><sourceid>gale_plos_</sourceid><recordid>TN_cdi_plos_journals_1327184099</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><galeid>A477066290</galeid><doaj_id>oai_doaj_org_article_755950a4c5214302be9eb8cac96b0847</doaj_id><sourcerecordid>A477066290</sourcerecordid><originalsourceid>FETCH-LOGICAL-c692t-47834b327ae1bc9608cc1997fb200a05e7ffe23fdc5f1a5d816e9b731b6d76a13</originalsourceid><addsrcrecordid>eNqNkl2L1DAUhoso7rr6D0QLgrgXHfPVpLkRhuquAwMjunob0jTpZMg0s00r-u9Nne4ylb2QXCScPOc9OSdvkryEYAExg-93fuha6RYH3-oFADnEHDxKziHHKKMI4Mcn57PkWQi7COGC0qfJGcKoILQozpPNtW51J3vr29Sb1AytGs_SpeV6nYWDVtZYlSrf1WnlvK_T8madDsG2TVp-JCBztpG9rkc8XX4pnydPjHRBv5j2i-T71aeb8nO23lyvyuU6U5SjPiOswKTCiEkNK8UpKJSCnDNTIQAkyDUzRiNsapUbKPO6gFTzimFY0ZpRCfFF8vqoe3A-iGkWQcAoCQsCOI_E6kjUXu7EobN72f0WXlrxN-C7Rsiut8ppwfKc50ASlSNIMECV5roqlIwPq0BBWNT6MFUbqr2ulW77TrqZ6PymtVvR-J8C54hSCKLAu0mg87eDDr3Y26C0c7LVfojvRrE3BgkgEX3zD_pwdxPVyNiAbY2PddUoKpaEMUAp4mPZxQNUXLXeWxWNY2yMzxIuZwmR6fWvvpFDCGL17ev_s5sfc_btCbvV0vXb4N0wei3MQXIEVedD6LS5HzIEYvT93TTE6Hsx-T6mvTr9oPukO6PjP-6N-b4</addsrcrecordid><sourcetype>Open Website</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1327184099</pqid></control><display><type>article</type><title>Generation of functional CLL-specific cord blood CTL using CD40-ligated CLL APC</title><source>MEDLINE</source><source>DOAJ Directory of Open Access Journals</source><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><source>PubMed Central</source><source>Free Full-Text Journals in Chemistry</source><source>Public Library of Science (PLoS)</source><creator>Decker, William K ; Shah, Nina ; Xing, Dongxia ; Lapushin, Ruth ; Li, Sufang ; Robinson, Simon N ; Yang, Hong ; Parmar, Simrit ; Halpert, Matthew M ; Keating, Michael J ; Gribben, John G ; Molldrem, Jeffrey J ; Shpall, Elizabeth J ; Wierda, William G</creator><creatorcontrib>Decker, William K ; Shah, Nina ; Xing, Dongxia ; Lapushin, Ruth ; Li, Sufang ; Robinson, Simon N ; Yang, Hong ; Parmar, Simrit ; Halpert, Matthew M ; Keating, Michael J ; Gribben, John G ; Molldrem, Jeffrey J ; Shpall, Elizabeth J ; Wierda, William G</creatorcontrib><description>Though remissions have been observed following allo-HSCT for the treatment of CLL, many CLL patients are ineligible for transplant due to the lack of HLA-compatible donors. The use of umbilical cord blood (UCB) permits transplantation of many patients who lack HLA-compatible donors due to reduced requirements for stringent HLA matching between graft and recipient; however, disease relapse remains a concern with this modality. The generation of CLL-specific CTL from UCB T-cells, primed and expanded against the leukemic clone, might enhance the GVL effect and improve outcomes with UCB transplantation. Here we report the generation of functional, CLL-specific CTL using CD40-ligated CLL cells to prime partially-HLA matched UCB T-cells. Functionality and specificity were demonstrated by immune synapse assay, IFN-γ ELISpot, multi-parametric intracellular cytokine flow cytometry, and (51)Cr release assay. The use of patient-specific, non-CLL controls demonstrated the generation of both alloantigen and CLL-specific responses. Subsequently, we developed a clinically-applicable procedure permitting separation of alloreactive CTL from leukemia-specific CTL. Leukemia-specific CTL were able to mediate in vivo killing of CLL in humanized mice without concurrent or subsequent development of xenoGVHD. Our results demonstrate that generation of CLL-specific effectors from UCB is feasible and practical, and the results support further exploration of this strategy as a treatment modality for CLL.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0051390</identifier><identifier>PMID: 23284688</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Adult ; Animals ; Antigen-Presenting Cells - immunology ; Antigen-Presenting Cells - metabolism ; Antigens ; Antigens, Neoplasm - immunology ; Biology ; Blood ; Cancer ; CD40 antigen ; CD40 Antigens - immunology ; CD40 Antigens - metabolism ; Chromium radioisotopes ; Chronic illnesses ; Chronic lymphatic leukemia ; Chronic lymphocytic leukemia ; Cord blood ; Cytometry ; Cytotoxicity ; Donors ; Enzyme-linked immunosorbent assay ; Feasibility Studies ; Fetal Blood - immunology ; Flow cytometry ; Histocompatibility antigen HLA ; HLA Antigens - immunology ; Humans ; Immunological Synapses - immunology ; Immunology ; Interferon ; Killing ; Leukemia ; Leukemia, Lymphocytic, Chronic, B-Cell - immunology ; Lymphocytes ; Lymphocytes T ; Medicine ; Mice ; Patients ; Stem cell transplantation ; Stem cells ; String matching ; Synapses ; T cell receptors ; T cells ; T-Lymphocytes - immunology ; Transplantation ; Transplants &amp; implants ; Umbilical cord ; γ-Interferon</subject><ispartof>PloS one, 2012-12, Vol.7 (12), p.e51390-e51390</ispartof><rights>COPYRIGHT 2012 Public Library of Science</rights><rights>2012 Decker et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License: https://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2012 Decker et al 2012 Decker et al</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c692t-47834b327ae1bc9608cc1997fb200a05e7ffe23fdc5f1a5d816e9b731b6d76a13</citedby><cites>FETCH-LOGICAL-c692t-47834b327ae1bc9608cc1997fb200a05e7ffe23fdc5f1a5d816e9b731b6d76a13</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3526610/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3526610/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,860,881,2096,2915,23845,27901,27902,53766,53768,79343,79344</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23284688$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Decker, William K</creatorcontrib><creatorcontrib>Shah, Nina</creatorcontrib><creatorcontrib>Xing, Dongxia</creatorcontrib><creatorcontrib>Lapushin, Ruth</creatorcontrib><creatorcontrib>Li, Sufang</creatorcontrib><creatorcontrib>Robinson, Simon N</creatorcontrib><creatorcontrib>Yang, Hong</creatorcontrib><creatorcontrib>Parmar, Simrit</creatorcontrib><creatorcontrib>Halpert, Matthew M</creatorcontrib><creatorcontrib>Keating, Michael J</creatorcontrib><creatorcontrib>Gribben, John G</creatorcontrib><creatorcontrib>Molldrem, Jeffrey J</creatorcontrib><creatorcontrib>Shpall, Elizabeth J</creatorcontrib><creatorcontrib>Wierda, William G</creatorcontrib><title>Generation of functional CLL-specific cord blood CTL using CD40-ligated CLL APC</title><title>PloS one</title><addtitle>PLoS One</addtitle><description>Though remissions have been observed following allo-HSCT for the treatment of CLL, many CLL patients are ineligible for transplant due to the lack of HLA-compatible donors. The use of umbilical cord blood (UCB) permits transplantation of many patients who lack HLA-compatible donors due to reduced requirements for stringent HLA matching between graft and recipient; however, disease relapse remains a concern with this modality. The generation of CLL-specific CTL from UCB T-cells, primed and expanded against the leukemic clone, might enhance the GVL effect and improve outcomes with UCB transplantation. Here we report the generation of functional, CLL-specific CTL using CD40-ligated CLL cells to prime partially-HLA matched UCB T-cells. Functionality and specificity were demonstrated by immune synapse assay, IFN-γ ELISpot, multi-parametric intracellular cytokine flow cytometry, and (51)Cr release assay. The use of patient-specific, non-CLL controls demonstrated the generation of both alloantigen and CLL-specific responses. Subsequently, we developed a clinically-applicable procedure permitting separation of alloreactive CTL from leukemia-specific CTL. Leukemia-specific CTL were able to mediate in vivo killing of CLL in humanized mice without concurrent or subsequent development of xenoGVHD. Our results demonstrate that generation of CLL-specific effectors from UCB is feasible and practical, and the results support further exploration of this strategy as a treatment modality for CLL.</description><subject>Adult</subject><subject>Animals</subject><subject>Antigen-Presenting Cells - immunology</subject><subject>Antigen-Presenting Cells - metabolism</subject><subject>Antigens</subject><subject>Antigens, Neoplasm - immunology</subject><subject>Biology</subject><subject>Blood</subject><subject>Cancer</subject><subject>CD40 antigen</subject><subject>CD40 Antigens - immunology</subject><subject>CD40 Antigens - metabolism</subject><subject>Chromium radioisotopes</subject><subject>Chronic illnesses</subject><subject>Chronic lymphatic leukemia</subject><subject>Chronic lymphocytic leukemia</subject><subject>Cord blood</subject><subject>Cytometry</subject><subject>Cytotoxicity</subject><subject>Donors</subject><subject>Enzyme-linked immunosorbent assay</subject><subject>Feasibility Studies</subject><subject>Fetal Blood - immunology</subject><subject>Flow cytometry</subject><subject>Histocompatibility antigen HLA</subject><subject>HLA Antigens - immunology</subject><subject>Humans</subject><subject>Immunological Synapses - immunology</subject><subject>Immunology</subject><subject>Interferon</subject><subject>Killing</subject><subject>Leukemia</subject><subject>Leukemia, Lymphocytic, Chronic, B-Cell - immunology</subject><subject>Lymphocytes</subject><subject>Lymphocytes T</subject><subject>Medicine</subject><subject>Mice</subject><subject>Patients</subject><subject>Stem cell transplantation</subject><subject>Stem cells</subject><subject>String matching</subject><subject>Synapses</subject><subject>T cell receptors</subject><subject>T cells</subject><subject>T-Lymphocytes - immunology</subject><subject>Transplantation</subject><subject>Transplants &amp; implants</subject><subject>Umbilical cord</subject><subject>γ-Interferon</subject><issn>1932-6203</issn><issn>1932-6203</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><sourceid>DOA</sourceid><recordid>eNqNkl2L1DAUhoso7rr6D0QLgrgXHfPVpLkRhuquAwMjunob0jTpZMg0s00r-u9Nne4ylb2QXCScPOc9OSdvkryEYAExg-93fuha6RYH3-oFADnEHDxKziHHKKMI4Mcn57PkWQi7COGC0qfJGcKoILQozpPNtW51J3vr29Sb1AytGs_SpeV6nYWDVtZYlSrf1WnlvK_T8madDsG2TVp-JCBztpG9rkc8XX4pnydPjHRBv5j2i-T71aeb8nO23lyvyuU6U5SjPiOswKTCiEkNK8UpKJSCnDNTIQAkyDUzRiNsapUbKPO6gFTzimFY0ZpRCfFF8vqoe3A-iGkWQcAoCQsCOI_E6kjUXu7EobN72f0WXlrxN-C7Rsiut8ppwfKc50ASlSNIMECV5roqlIwPq0BBWNT6MFUbqr2ulW77TrqZ6PymtVvR-J8C54hSCKLAu0mg87eDDr3Y26C0c7LVfojvRrE3BgkgEX3zD_pwdxPVyNiAbY2PddUoKpaEMUAp4mPZxQNUXLXeWxWNY2yMzxIuZwmR6fWvvpFDCGL17ev_s5sfc_btCbvV0vXb4N0wei3MQXIEVedD6LS5HzIEYvT93TTE6Hsx-T6mvTr9oPukO6PjP-6N-b4</recordid><startdate>20121219</startdate><enddate>20121219</enddate><creator>Decker, William K</creator><creator>Shah, Nina</creator><creator>Xing, Dongxia</creator><creator>Lapushin, Ruth</creator><creator>Li, Sufang</creator><creator>Robinson, Simon N</creator><creator>Yang, Hong</creator><creator>Parmar, Simrit</creator><creator>Halpert, Matthew M</creator><creator>Keating, Michael J</creator><creator>Gribben, John G</creator><creator>Molldrem, Jeffrey J</creator><creator>Shpall, Elizabeth J</creator><creator>Wierda, William G</creator><general>Public Library of Science</general><general>Public Library of Science (PLoS)</general><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>IOV</scope><scope>ISR</scope><scope>3V.</scope><scope>7QG</scope><scope>7QL</scope><scope>7QO</scope><scope>7RV</scope><scope>7SN</scope><scope>7SS</scope><scope>7T5</scope><scope>7TG</scope><scope>7TM</scope><scope>7U9</scope><scope>7X2</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABJCF</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>ARAPS</scope><scope>ATCPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>D1I</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>KB.</scope><scope>KB0</scope><scope>KL.</scope><scope>L6V</scope><scope>LK8</scope><scope>M0K</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>M7P</scope><scope>M7S</scope><scope>NAPCQ</scope><scope>P5Z</scope><scope>P62</scope><scope>P64</scope><scope>PATMY</scope><scope>PDBOC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>PTHSS</scope><scope>PYCSY</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20121219</creationdate><title>Generation of functional CLL-specific cord blood CTL using CD40-ligated CLL APC</title><author>Decker, William K ; Shah, Nina ; Xing, Dongxia ; Lapushin, Ruth ; Li, Sufang ; Robinson, Simon N ; Yang, Hong ; Parmar, Simrit ; Halpert, Matthew M ; Keating, Michael J ; Gribben, John G ; Molldrem, Jeffrey J ; Shpall, Elizabeth J ; Wierda, William G</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c692t-47834b327ae1bc9608cc1997fb200a05e7ffe23fdc5f1a5d816e9b731b6d76a13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Adult</topic><topic>Animals</topic><topic>Antigen-Presenting Cells - immunology</topic><topic>Antigen-Presenting Cells - metabolism</topic><topic>Antigens</topic><topic>Antigens, Neoplasm - immunology</topic><topic>Biology</topic><topic>Blood</topic><topic>Cancer</topic><topic>CD40 antigen</topic><topic>CD40 Antigens - immunology</topic><topic>CD40 Antigens - metabolism</topic><topic>Chromium radioisotopes</topic><topic>Chronic illnesses</topic><topic>Chronic lymphatic leukemia</topic><topic>Chronic lymphocytic leukemia</topic><topic>Cord blood</topic><topic>Cytometry</topic><topic>Cytotoxicity</topic><topic>Donors</topic><topic>Enzyme-linked immunosorbent assay</topic><topic>Feasibility Studies</topic><topic>Fetal Blood - immunology</topic><topic>Flow cytometry</topic><topic>Histocompatibility antigen HLA</topic><topic>HLA Antigens - immunology</topic><topic>Humans</topic><topic>Immunological Synapses - immunology</topic><topic>Immunology</topic><topic>Interferon</topic><topic>Killing</topic><topic>Leukemia</topic><topic>Leukemia, Lymphocytic, Chronic, B-Cell - immunology</topic><topic>Lymphocytes</topic><topic>Lymphocytes T</topic><topic>Medicine</topic><topic>Mice</topic><topic>Patients</topic><topic>Stem cell transplantation</topic><topic>Stem cells</topic><topic>String matching</topic><topic>Synapses</topic><topic>T cell receptors</topic><topic>T cells</topic><topic>T-Lymphocytes - immunology</topic><topic>Transplantation</topic><topic>Transplants &amp; implants</topic><topic>Umbilical cord</topic><topic>γ-Interferon</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Decker, William K</creatorcontrib><creatorcontrib>Shah, Nina</creatorcontrib><creatorcontrib>Xing, Dongxia</creatorcontrib><creatorcontrib>Lapushin, Ruth</creatorcontrib><creatorcontrib>Li, Sufang</creatorcontrib><creatorcontrib>Robinson, Simon N</creatorcontrib><creatorcontrib>Yang, Hong</creatorcontrib><creatorcontrib>Parmar, Simrit</creatorcontrib><creatorcontrib>Halpert, Matthew M</creatorcontrib><creatorcontrib>Keating, Michael J</creatorcontrib><creatorcontrib>Gribben, John G</creatorcontrib><creatorcontrib>Molldrem, Jeffrey J</creatorcontrib><creatorcontrib>Shpall, Elizabeth J</creatorcontrib><creatorcontrib>Wierda, William G</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Gale In Context: Opposing Viewpoints</collection><collection>Gale In Context: Science</collection><collection>ProQuest Central (Corporate)</collection><collection>Animal Behavior Abstracts</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Biotechnology Research Abstracts</collection><collection>Nursing &amp; Allied Health Database</collection><collection>Ecology Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Immunology Abstracts</collection><collection>Meteorological &amp; Geoastrophysical Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Agricultural Science Collection</collection><collection>Health &amp; Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Technology 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>Materials Science &amp; Engineering Collection</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest One Sustainability</collection><collection>ProQuest Central UK/Ireland</collection><collection>Advanced Technologies &amp; Aerospace Collection</collection><collection>Agricultural &amp; Environmental Science Collection</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Technology Collection</collection><collection>Natural Science Collection</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Materials Science Collection</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 &amp; Medical Complete (Alumni)</collection><collection>Materials Science Database</collection><collection>Nursing &amp; Allied Health Database (Alumni Edition)</collection><collection>Meteorological &amp; Geoastrophysical Abstracts - Academic</collection><collection>ProQuest Engineering Collection</collection><collection>ProQuest Biological Science Collection</collection><collection>Agricultural Science Database</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biological Science Database</collection><collection>Engineering Database</collection><collection>Nursing &amp; Allied Health Premium</collection><collection>Advanced Technologies &amp; Aerospace Database</collection><collection>ProQuest Advanced Technologies &amp; Aerospace Collection</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Environmental Science Database</collection><collection>Materials Science Collection</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>Engineering Collection</collection><collection>Environmental Science Collection</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>PloS one</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Decker, William K</au><au>Shah, Nina</au><au>Xing, Dongxia</au><au>Lapushin, Ruth</au><au>Li, Sufang</au><au>Robinson, Simon N</au><au>Yang, Hong</au><au>Parmar, Simrit</au><au>Halpert, Matthew M</au><au>Keating, Michael J</au><au>Gribben, John G</au><au>Molldrem, Jeffrey J</au><au>Shpall, Elizabeth J</au><au>Wierda, William G</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Generation of functional CLL-specific cord blood CTL using CD40-ligated CLL APC</atitle><jtitle>PloS one</jtitle><addtitle>PLoS One</addtitle><date>2012-12-19</date><risdate>2012</risdate><volume>7</volume><issue>12</issue><spage>e51390</spage><epage>e51390</epage><pages>e51390-e51390</pages><issn>1932-6203</issn><eissn>1932-6203</eissn><abstract>Though remissions have been observed following allo-HSCT for the treatment of CLL, many CLL patients are ineligible for transplant due to the lack of HLA-compatible donors. The use of umbilical cord blood (UCB) permits transplantation of many patients who lack HLA-compatible donors due to reduced requirements for stringent HLA matching between graft and recipient; however, disease relapse remains a concern with this modality. The generation of CLL-specific CTL from UCB T-cells, primed and expanded against the leukemic clone, might enhance the GVL effect and improve outcomes with UCB transplantation. Here we report the generation of functional, CLL-specific CTL using CD40-ligated CLL cells to prime partially-HLA matched UCB T-cells. Functionality and specificity were demonstrated by immune synapse assay, IFN-γ ELISpot, multi-parametric intracellular cytokine flow cytometry, and (51)Cr release assay. The use of patient-specific, non-CLL controls demonstrated the generation of both alloantigen and CLL-specific responses. Subsequently, we developed a clinically-applicable procedure permitting separation of alloreactive CTL from leukemia-specific CTL. Leukemia-specific CTL were able to mediate in vivo killing of CLL in humanized mice without concurrent or subsequent development of xenoGVHD. Our results demonstrate that generation of CLL-specific effectors from UCB is feasible and practical, and the results support further exploration of this strategy as a treatment modality for CLL.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>23284688</pmid><doi>10.1371/journal.pone.0051390</doi><tpages>e51390</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 1932-6203
ispartof PloS one, 2012-12, Vol.7 (12), p.e51390-e51390
issn 1932-6203
1932-6203
language eng
recordid cdi_plos_journals_1327184099
source MEDLINE; DOAJ Directory of Open Access Journals; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; PubMed Central; Free Full-Text Journals in Chemistry; Public Library of Science (PLoS)
subjects Adult
Animals
Antigen-Presenting Cells - immunology
Antigen-Presenting Cells - metabolism
Antigens
Antigens, Neoplasm - immunology
Biology
Blood
Cancer
CD40 antigen
CD40 Antigens - immunology
CD40 Antigens - metabolism
Chromium radioisotopes
Chronic illnesses
Chronic lymphatic leukemia
Chronic lymphocytic leukemia
Cord blood
Cytometry
Cytotoxicity
Donors
Enzyme-linked immunosorbent assay
Feasibility Studies
Fetal Blood - immunology
Flow cytometry
Histocompatibility antigen HLA
HLA Antigens - immunology
Humans
Immunological Synapses - immunology
Immunology
Interferon
Killing
Leukemia
Leukemia, Lymphocytic, Chronic, B-Cell - immunology
Lymphocytes
Lymphocytes T
Medicine
Mice
Patients
Stem cell transplantation
Stem cells
String matching
Synapses
T cell receptors
T cells
T-Lymphocytes - immunology
Transplantation
Transplants & implants
Umbilical cord
γ-Interferon
title Generation of functional CLL-specific cord blood CTL using CD40-ligated CLL APC
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-04T01%3A54%3A17IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_plos_&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Generation%20of%20functional%20CLL-specific%20cord%20blood%20CTL%20using%20CD40-ligated%20CLL%20APC&rft.jtitle=PloS%20one&rft.au=Decker,%20William%20K&rft.date=2012-12-19&rft.volume=7&rft.issue=12&rft.spage=e51390&rft.epage=e51390&rft.pages=e51390-e51390&rft.issn=1932-6203&rft.eissn=1932-6203&rft_id=info:doi/10.1371/journal.pone.0051390&rft_dat=%3Cgale_plos_%3EA477066290%3C/gale_plos_%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1327184099&rft_id=info:pmid/23284688&rft_galeid=A477066290&rft_doaj_id=oai_doaj_org_article_755950a4c5214302be9eb8cac96b0847&rfr_iscdi=true