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The histone deacetylase inhibitor, romidepsin, suppresses cellular immune functions of cutaneous T-cell lymphoma patients
Romidepsin is the second histone deacetylase inhibitor (HDACi) approved for the treatment of advanced stages of cutaneous T‐cell lymphoma (CTCL). Recent in vitro data suggest that HDACis suppress immune function although these findings have not been confirmed in patients. Thus, we serially examined...
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Published in: | American journal of hematology 2012-04, Vol.87 (4), p.354-360 |
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creator | Kelly-Sell, Michael J. Kim, Youn H. Straus, Suzanne Benoit, Bernice Harrison, Cameron Sutherland, Katherine Armstrong, Randall Weng, Wen-Kai Showe, Louise C. Wysocka, Maria Rook, Alain H. |
description | Romidepsin is the second histone deacetylase inhibitor (HDACi) approved for the treatment of advanced stages of cutaneous T‐cell lymphoma (CTCL). Recent in vitro data suggest that HDACis suppress immune function although these findings have not been confirmed in patients. Thus, we serially examined the cellular immune function of eight CTCL patients undergoing treatment with three cycles of romidepsin. We measured the patients' natural killer (NK) and dendritic cell (DC) function and performed an in vitro terminal deoxynucleotidyl transferase dUTP nick end labeling assay to measure cellular apoptosis. Patients' NK cell cytolytic activity decreased from baseline to the third cycle of treatment (P = 0.018) but stimulation with a toll‐like receptor (TLR) agonist increased this activity (P = 0.018). At baseline, a TLR agonist could both activate patients' DC (P = 0.043) and stimulate interleukin‐12 protein production (P = 0.043) but both were suppressed after the first cycle of romidepsin. Finally, we observed increased specificity for romidepsin‐induced CD4+ tumor cell apoptosis and dose‐dependent increases in cellular apoptosis of healthy cells in multiple lineages (P < 0.05). These findings raise concern that HDACis suppress immune function in CTCL patients and they support the concurrent use of multiple immune stimulatory agents to preserve the host immune response. Am. J. Hematol. 2012. © 2012 Wiley Periodicals, Inc. |
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Recent in vitro data suggest that HDACis suppress immune function although these findings have not been confirmed in patients. Thus, we serially examined the cellular immune function of eight CTCL patients undergoing treatment with three cycles of romidepsin. We measured the patients' natural killer (NK) and dendritic cell (DC) function and performed an in vitro terminal deoxynucleotidyl transferase dUTP nick end labeling assay to measure cellular apoptosis. Patients' NK cell cytolytic activity decreased from baseline to the third cycle of treatment (P = 0.018) but stimulation with a toll‐like receptor (TLR) agonist increased this activity (P = 0.018). At baseline, a TLR agonist could both activate patients' DC (P = 0.043) and stimulate interleukin‐12 protein production (P = 0.043) but both were suppressed after the first cycle of romidepsin. Finally, we observed increased specificity for romidepsin‐induced CD4+ tumor cell apoptosis and dose‐dependent increases in cellular apoptosis of healthy cells in multiple lineages (P < 0.05). These findings raise concern that HDACis suppress immune function in CTCL patients and they support the concurrent use of multiple immune stimulatory agents to preserve the host immune response. Am. J. Hematol. 2012. © 2012 Wiley Periodicals, Inc.</description><identifier>ISSN: 0361-8609</identifier><identifier>EISSN: 1096-8652</identifier><identifier>DOI: 10.1002/ajh.23112</identifier><identifier>PMID: 22367792</identifier><identifier>CODEN: AJHEDD</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Adjuvants, Immunologic - therapeutic use ; Apoptosis - drug effects ; Biological and medical sciences ; Cells, Cultured - drug effects ; Cells, Cultured - immunology ; Cytotoxicity, Immunologic - drug effects ; Depression, Chemical ; Depsipeptides - adverse effects ; Depsipeptides - pharmacology ; Depsipeptides - therapeutic use ; Drug Screening Assays, Antitumor ; Hematologic and hematopoietic diseases ; Hematology ; Histone Deacetylase Inhibitors - adverse effects ; Histone Deacetylase Inhibitors - pharmacology ; Histone Deacetylase Inhibitors - therapeutic use ; Humans ; Imidazoles - pharmacology ; Immunity, Cellular - drug effects ; In Vitro Techniques ; Interferon-alpha - pharmacology ; Interleukin-12 - pharmacology ; Killer Cells, Natural - drug effects ; Leukocytes, Mononuclear - drug effects ; Leukocytes, Mononuclear - immunology ; Lymphocyte Count ; Lysosomal-Associated Membrane Protein 1 - analysis ; Medical sciences ; Neoplasm Proteins - antagonists & inhibitors ; Quinolines - pharmacology ; Sezary Syndrome - drug therapy ; Sezary Syndrome - immunology ; Skin Neoplasms - drug therapy ; Skin Neoplasms - immunology ; T-Lymphocytes, Regulatory - drug effects ; Toll-Like Receptor 7 - agonists ; Toll-Like Receptor 8 - agonists</subject><ispartof>American journal of hematology, 2012-04, Vol.87 (4), p.354-360</ispartof><rights>Copyright © 2012 Wiley Periodicals, Inc.</rights><rights>2015 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5102-daa92eee3a51bb91f3c98b251af37ae3c05947cff3ff87e7cb39cea53d8561683</citedby><cites>FETCH-LOGICAL-c5102-daa92eee3a51bb91f3c98b251af37ae3c05947cff3ff87e7cb39cea53d8561683</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=25646431$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22367792$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kelly-Sell, Michael J.</creatorcontrib><creatorcontrib>Kim, Youn H.</creatorcontrib><creatorcontrib>Straus, Suzanne</creatorcontrib><creatorcontrib>Benoit, Bernice</creatorcontrib><creatorcontrib>Harrison, Cameron</creatorcontrib><creatorcontrib>Sutherland, Katherine</creatorcontrib><creatorcontrib>Armstrong, Randall</creatorcontrib><creatorcontrib>Weng, Wen-Kai</creatorcontrib><creatorcontrib>Showe, Louise C.</creatorcontrib><creatorcontrib>Wysocka, Maria</creatorcontrib><creatorcontrib>Rook, Alain H.</creatorcontrib><title>The histone deacetylase inhibitor, romidepsin, suppresses cellular immune functions of cutaneous T-cell lymphoma patients</title><title>American journal of hematology</title><addtitle>Am. J. Hematol</addtitle><description>Romidepsin is the second histone deacetylase inhibitor (HDACi) approved for the treatment of advanced stages of cutaneous T‐cell lymphoma (CTCL). Recent in vitro data suggest that HDACis suppress immune function although these findings have not been confirmed in patients. Thus, we serially examined the cellular immune function of eight CTCL patients undergoing treatment with three cycles of romidepsin. We measured the patients' natural killer (NK) and dendritic cell (DC) function and performed an in vitro terminal deoxynucleotidyl transferase dUTP nick end labeling assay to measure cellular apoptosis. Patients' NK cell cytolytic activity decreased from baseline to the third cycle of treatment (P = 0.018) but stimulation with a toll‐like receptor (TLR) agonist increased this activity (P = 0.018). At baseline, a TLR agonist could both activate patients' DC (P = 0.043) and stimulate interleukin‐12 protein production (P = 0.043) but both were suppressed after the first cycle of romidepsin. Finally, we observed increased specificity for romidepsin‐induced CD4+ tumor cell apoptosis and dose‐dependent increases in cellular apoptosis of healthy cells in multiple lineages (P < 0.05). These findings raise concern that HDACis suppress immune function in CTCL patients and they support the concurrent use of multiple immune stimulatory agents to preserve the host immune response. Am. J. 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J. Hematol</addtitle><date>2012-04</date><risdate>2012</risdate><volume>87</volume><issue>4</issue><spage>354</spage><epage>360</epage><pages>354-360</pages><issn>0361-8609</issn><eissn>1096-8652</eissn><coden>AJHEDD</coden><abstract>Romidepsin is the second histone deacetylase inhibitor (HDACi) approved for the treatment of advanced stages of cutaneous T‐cell lymphoma (CTCL). Recent in vitro data suggest that HDACis suppress immune function although these findings have not been confirmed in patients. Thus, we serially examined the cellular immune function of eight CTCL patients undergoing treatment with three cycles of romidepsin. We measured the patients' natural killer (NK) and dendritic cell (DC) function and performed an in vitro terminal deoxynucleotidyl transferase dUTP nick end labeling assay to measure cellular apoptosis. Patients' NK cell cytolytic activity decreased from baseline to the third cycle of treatment (P = 0.018) but stimulation with a toll‐like receptor (TLR) agonist increased this activity (P = 0.018). At baseline, a TLR agonist could both activate patients' DC (P = 0.043) and stimulate interleukin‐12 protein production (P = 0.043) but both were suppressed after the first cycle of romidepsin. Finally, we observed increased specificity for romidepsin‐induced CD4+ tumor cell apoptosis and dose‐dependent increases in cellular apoptosis of healthy cells in multiple lineages (P < 0.05). These findings raise concern that HDACis suppress immune function in CTCL patients and they support the concurrent use of multiple immune stimulatory agents to preserve the host immune response. Am. J. Hematol. 2012. © 2012 Wiley Periodicals, Inc.</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>22367792</pmid><doi>10.1002/ajh.23112</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adjuvants, Immunologic - therapeutic use Apoptosis - drug effects Biological and medical sciences Cells, Cultured - drug effects Cells, Cultured - immunology Cytotoxicity, Immunologic - drug effects Depression, Chemical Depsipeptides - adverse effects Depsipeptides - pharmacology Depsipeptides - therapeutic use Drug Screening Assays, Antitumor Hematologic and hematopoietic diseases Hematology Histone Deacetylase Inhibitors - adverse effects Histone Deacetylase Inhibitors - pharmacology Histone Deacetylase Inhibitors - therapeutic use Humans Imidazoles - pharmacology Immunity, Cellular - drug effects In Vitro Techniques Interferon-alpha - pharmacology Interleukin-12 - pharmacology Killer Cells, Natural - drug effects Leukocytes, Mononuclear - drug effects Leukocytes, Mononuclear - immunology Lymphocyte Count Lysosomal-Associated Membrane Protein 1 - analysis Medical sciences Neoplasm Proteins - antagonists & inhibitors Quinolines - pharmacology Sezary Syndrome - drug therapy Sezary Syndrome - immunology Skin Neoplasms - drug therapy Skin Neoplasms - immunology T-Lymphocytes, Regulatory - drug effects Toll-Like Receptor 7 - agonists Toll-Like Receptor 8 - agonists |
title | The histone deacetylase inhibitor, romidepsin, suppresses cellular immune functions of cutaneous T-cell lymphoma patients |
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