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...
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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 |
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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 & 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. 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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 - 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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> |
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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 |