Autologous bone marrow Th cells can support multiple myeloma cell proliferation in vitro and in xenografted mice
Multiple myeloma (MM) is a plasma cell malignancy where MM cell growth is supported by the bone marrow (BM) microenvironment with poorly defined cellular and molecular mechanisms. MM cells express CD40, a receptor known to activate autocrine secretion of cytokines and elicit proliferation. Activated...
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creator | Wang, D Fløisand, Y Myklebust, C V Bürgler, S Parente-Ribes, A Hofgaard, P O Bogen, B Taskén, K Tjønnfjord, G E Schjesvold, F Dalgaard, J Tveita, A Munthe, L A |
description | Multiple myeloma (MM) is a plasma cell malignancy where MM cell growth is supported by the bone marrow (BM) microenvironment with poorly defined cellular and molecular mechanisms. MM cells express CD40, a receptor known to activate autocrine secretion of cytokines and elicit proliferation. Activated T helper (Th) cells express CD40 ligand (CD40L) and BM Th cells are significantly increased in MM patients. We hypothesized that activated BM Th cells could support MM cell growth. We here found that activated autologous BM Th cells supported MM cell growth in a contact- and CD40L-dependent manner
in vitro.
MM cells had retained the ability to activate Th cells that reciprocated and stimulated MM cell proliferation. Autologous BM Th cells supported MM cell growth in xenografted mice and were found in close contact with MM cells. MM cells secreted chemokines that attracted Th cells, secretion was augmented by CD40-stimulation. Within 14 days of culture of whole BM aspirates in autologous serum, MM cells and Th cells mutually stimulated each other, and MM cells required Th cells for further expansion
in vitro
and in mice. The results suggest that Th cells may support the expansion of MM cells in patients. |
doi_str_mv | 10.1038/leu.2017.69 |
format | Article |
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in vitro.
MM cells had retained the ability to activate Th cells that reciprocated and stimulated MM cell proliferation. Autologous BM Th cells supported MM cell growth in xenografted mice and were found in close contact with MM cells. MM cells secreted chemokines that attracted Th cells, secretion was augmented by CD40-stimulation. Within 14 days of culture of whole BM aspirates in autologous serum, MM cells and Th cells mutually stimulated each other, and MM cells required Th cells for further expansion
in vitro
and in mice. The results suggest that Th cells may support the expansion of MM cells in patients.</description><identifier>ISSN: 0887-6924</identifier><identifier>EISSN: 1476-5551</identifier><identifier>DOI: 10.1038/leu.2017.69</identifier><identifier>PMID: 28232741</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>631/67 ; 631/67/1990/804 ; Aged ; Animals ; Antigen Presentation ; Autocrine signalling ; Autografts ; Bone marrow ; Bone Marrow Transplantation - adverse effects ; Cancer Research ; Care and treatment ; CD40 antigen ; CD40 Antigens - immunology ; CD40 Ligand - immunology ; CD40L protein ; Cell culture ; Cell Division ; Cell growth ; Cell proliferation ; Chemokines ; Chemokines - secretion ; Chemotaxis, Leukocyte ; Coculture Techniques ; Critical Care Medicine ; Cytokines ; Cytokines - secretion ; Development and progression ; Graft Survival - immunology ; Health aspects ; Helper cells ; Hematology ; Heterografts ; Humans ; Intensive ; Internal Medicine ; Lymphocyte Activation ; Lymphocytes T ; Malignancy ; Medicine ; Medicine & Public Health ; Mice ; Mice, Inbred NOD ; Mice, SCID ; Microenvironments ; Middle Aged ; Molecular modelling ; Multiple myeloma ; Multiple Myeloma - pathology ; Multiple Myeloma - secretion ; Multiple Myeloma - therapy ; Oncology ; original-article ; Patients ; T cells ; T-Lymphocytes, Helper-Inducer - immunology ; T-Lymphocytes, Helper-Inducer - transplantation ; Transplantation, Autologous - adverse effects ; Tumor Escape - immunology ; Tumor Microenvironment ; Xenografts</subject><ispartof>Leukemia, 2017-10, Vol.31 (10), p.2114-2121</ispartof><rights>Macmillan Publishers Limited, part of Springer Nature. 2017</rights><rights>COPYRIGHT 2017 Nature Publishing Group</rights><rights>Copyright Nature Publishing Group Oct 2017</rights><rights>Macmillan Publishers Limited, part of Springer Nature. 2017.</rights><rights>info:eu-repo/semantics/openAccess</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c504t-8bbe5560f057bfedb937418efef4fb134fdaadaafc265eb4c1eeae6f621f29323</citedby><cites>FETCH-LOGICAL-c504t-8bbe5560f057bfedb937418efef4fb134fdaadaafc265eb4c1eeae6f621f29323</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/leu.2017.69$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1038/leu.2017.69$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>230,314,776,780,881,26544,27901,27902,41464,42533,51294</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28232741$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Wang, D</creatorcontrib><creatorcontrib>Fløisand, Y</creatorcontrib><creatorcontrib>Myklebust, C V</creatorcontrib><creatorcontrib>Bürgler, S</creatorcontrib><creatorcontrib>Parente-Ribes, A</creatorcontrib><creatorcontrib>Hofgaard, P O</creatorcontrib><creatorcontrib>Bogen, B</creatorcontrib><creatorcontrib>Taskén, K</creatorcontrib><creatorcontrib>Tjønnfjord, G E</creatorcontrib><creatorcontrib>Schjesvold, F</creatorcontrib><creatorcontrib>Dalgaard, J</creatorcontrib><creatorcontrib>Tveita, A</creatorcontrib><creatorcontrib>Munthe, L A</creatorcontrib><title>Autologous bone marrow Th cells can support multiple myeloma cell proliferation in vitro and in xenografted mice</title><title>Leukemia</title><addtitle>Leukemia</addtitle><addtitle>Leukemia</addtitle><description>Multiple myeloma (MM) is a plasma cell malignancy where MM cell growth is supported by the bone marrow (BM) microenvironment with poorly defined cellular and molecular mechanisms. MM cells express CD40, a receptor known to activate autocrine secretion of cytokines and elicit proliferation. Activated T helper (Th) cells express CD40 ligand (CD40L) and BM Th cells are significantly increased in MM patients. We hypothesized that activated BM Th cells could support MM cell growth. We here found that activated autologous BM Th cells supported MM cell growth in a contact- and CD40L-dependent manner
in vitro.
MM cells had retained the ability to activate Th cells that reciprocated and stimulated MM cell proliferation. Autologous BM Th cells supported MM cell growth in xenografted mice and were found in close contact with MM cells. MM cells secreted chemokines that attracted Th cells, secretion was augmented by CD40-stimulation. Within 14 days of culture of whole BM aspirates in autologous serum, MM cells and Th cells mutually stimulated each other, and MM cells required Th cells for further expansion
in vitro
and in mice. The results suggest that Th cells may support the expansion of MM cells in patients.</description><subject>631/67</subject><subject>631/67/1990/804</subject><subject>Aged</subject><subject>Animals</subject><subject>Antigen Presentation</subject><subject>Autocrine signalling</subject><subject>Autografts</subject><subject>Bone marrow</subject><subject>Bone Marrow Transplantation - adverse effects</subject><subject>Cancer Research</subject><subject>Care and treatment</subject><subject>CD40 antigen</subject><subject>CD40 Antigens - immunology</subject><subject>CD40 Ligand - immunology</subject><subject>CD40L protein</subject><subject>Cell culture</subject><subject>Cell Division</subject><subject>Cell growth</subject><subject>Cell proliferation</subject><subject>Chemokines</subject><subject>Chemokines - secretion</subject><subject>Chemotaxis, Leukocyte</subject><subject>Coculture Techniques</subject><subject>Critical Care Medicine</subject><subject>Cytokines</subject><subject>Cytokines - secretion</subject><subject>Development and progression</subject><subject>Graft Survival - immunology</subject><subject>Health aspects</subject><subject>Helper cells</subject><subject>Hematology</subject><subject>Heterografts</subject><subject>Humans</subject><subject>Intensive</subject><subject>Internal Medicine</subject><subject>Lymphocyte Activation</subject><subject>Lymphocytes T</subject><subject>Malignancy</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Mice</subject><subject>Mice, Inbred NOD</subject><subject>Mice, SCID</subject><subject>Microenvironments</subject><subject>Middle Aged</subject><subject>Molecular modelling</subject><subject>Multiple myeloma</subject><subject>Multiple Myeloma - pathology</subject><subject>Multiple Myeloma - secretion</subject><subject>Multiple Myeloma - therapy</subject><subject>Oncology</subject><subject>original-article</subject><subject>Patients</subject><subject>T cells</subject><subject>T-Lymphocytes, Helper-Inducer - immunology</subject><subject>T-Lymphocytes, Helper-Inducer - transplantation</subject><subject>Transplantation, Autologous - adverse effects</subject><subject>Tumor Escape - immunology</subject><subject>Tumor Microenvironment</subject><subject>Xenografts</subject><issn>0887-6924</issn><issn>1476-5551</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><sourceid>3HK</sourceid><recordid>eNp9kl1vFCEUhidGY7fVK--VxMSY6K7AAMNcbpr6kTTxpl4TZuawS8PACIzafy_TbZvWNAYSAjzn6z2nql4RvCG4lp8czBuKSbMR7ZNqRVgj1pxz8rRaYSmbtWgpO6qOU7rEePkUz6sjKmlNG0ZW1bSdc3BhF-aEuuABjTrG8Btd7FEPziXUa4_SPE0hZjTOLtvJFegKXBj1NYKmGJw1EHW2wSPr0S-bY0DaD8vlD_iwi9pkGNBoe3hRPTPaJXh5c55UPz6fXZx-XZ9___LtdHu-7jlmeS27DjgX2GDedAaGrq1LvhIMGGY6UjMzaF226ang0LGeAGgQRlBiaFvT-qR6c_DbR5uy9cqHqBXBklMlGGGkEO8PRCng5wwpq9GmpSLtocihiGwol1iKpqBv_0Evwxx9yV9RQTiva1z_lyItE0VwVtA7aqcdKOtNyFH3S2i15bhpMcHXETePUGUNUFQsjTK2vD8weHfPYA_a5X0Kbl6akh6CH26FCSlFMGqKtnT9qoijloFSZaDUMlBKtIV-fVPT3I0w3LG3E1SAjwcglS-_g3iv6Ef8_QUp2tKW</recordid><startdate>20171001</startdate><enddate>20171001</enddate><creator>Wang, D</creator><creator>Fløisand, Y</creator><creator>Myklebust, C V</creator><creator>Bürgler, S</creator><creator>Parente-Ribes, A</creator><creator>Hofgaard, P O</creator><creator>Bogen, B</creator><creator>Taskén, K</creator><creator>Tjønnfjord, G E</creator><creator>Schjesvold, F</creator><creator>Dalgaard, J</creator><creator>Tveita, A</creator><creator>Munthe, L A</creator><general>Nature Publishing Group UK</general><general>Nature Publishing Group</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>3V.</scope><scope>7QL</scope><scope>7RV</scope><scope>7T5</scope><scope>7T7</scope><scope>7TM</scope><scope>7TO</scope><scope>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</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>C1K</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>KB0</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>M7P</scope><scope>NAPCQ</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>3HK</scope></search><sort><creationdate>20171001</creationdate><title>Autologous bone marrow Th cells can support multiple myeloma cell proliferation in vitro and in xenografted mice</title><author>Wang, D ; Fløisand, Y ; Myklebust, C V ; Bürgler, S ; Parente-Ribes, A ; Hofgaard, P O ; Bogen, B ; Taskén, K ; Tjønnfjord, G E ; Schjesvold, F ; Dalgaard, J ; Tveita, A ; Munthe, L A</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c504t-8bbe5560f057bfedb937418efef4fb134fdaadaafc265eb4c1eeae6f621f29323</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>631/67</topic><topic>631/67/1990/804</topic><topic>Aged</topic><topic>Animals</topic><topic>Antigen Presentation</topic><topic>Autocrine signalling</topic><topic>Autografts</topic><topic>Bone marrow</topic><topic>Bone Marrow Transplantation - adverse effects</topic><topic>Cancer Research</topic><topic>Care and treatment</topic><topic>CD40 antigen</topic><topic>CD40 Antigens - immunology</topic><topic>CD40 Ligand - immunology</topic><topic>CD40L protein</topic><topic>Cell culture</topic><topic>Cell Division</topic><topic>Cell growth</topic><topic>Cell proliferation</topic><topic>Chemokines</topic><topic>Chemokines - secretion</topic><topic>Chemotaxis, Leukocyte</topic><topic>Coculture Techniques</topic><topic>Critical Care Medicine</topic><topic>Cytokines</topic><topic>Cytokines - secretion</topic><topic>Development and progression</topic><topic>Graft Survival - immunology</topic><topic>Health aspects</topic><topic>Helper cells</topic><topic>Hematology</topic><topic>Heterografts</topic><topic>Humans</topic><topic>Intensive</topic><topic>Internal Medicine</topic><topic>Lymphocyte Activation</topic><topic>Lymphocytes T</topic><topic>Malignancy</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Mice</topic><topic>Mice, Inbred NOD</topic><topic>Mice, SCID</topic><topic>Microenvironments</topic><topic>Middle Aged</topic><topic>Molecular modelling</topic><topic>Multiple myeloma</topic><topic>Multiple Myeloma - pathology</topic><topic>Multiple Myeloma - secretion</topic><topic>Multiple Myeloma - therapy</topic><topic>Oncology</topic><topic>original-article</topic><topic>Patients</topic><topic>T cells</topic><topic>T-Lymphocytes, Helper-Inducer - immunology</topic><topic>T-Lymphocytes, Helper-Inducer - transplantation</topic><topic>Transplantation, Autologous - adverse effects</topic><topic>Tumor Escape - immunology</topic><topic>Tumor Microenvironment</topic><topic>Xenografts</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wang, D</creatorcontrib><creatorcontrib>Fløisand, Y</creatorcontrib><creatorcontrib>Myklebust, C V</creatorcontrib><creatorcontrib>Bürgler, S</creatorcontrib><creatorcontrib>Parente-Ribes, A</creatorcontrib><creatorcontrib>Hofgaard, P O</creatorcontrib><creatorcontrib>Bogen, B</creatorcontrib><creatorcontrib>Taskén, K</creatorcontrib><creatorcontrib>Tjønnfjord, G E</creatorcontrib><creatorcontrib>Schjesvold, F</creatorcontrib><creatorcontrib>Dalgaard, J</creatorcontrib><creatorcontrib>Tveita, A</creatorcontrib><creatorcontrib>Munthe, L A</creatorcontrib><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>Bacteriology Abstracts (Microbiology B)</collection><collection>Nursing & Allied Health Database</collection><collection>Immunology Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Nucleic Acids Abstracts</collection><collection>Oncogenes and Growth Factors 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>Public Health Database</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>Environmental Sciences and Pollution Management</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>Nursing & Allied Health Database (Alumni Edition)</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>Nursing & Allied Health Premium</collection><collection>Biotechnology and BioEngineering Abstracts</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>MEDLINE - Academic</collection><collection>NORA - Norwegian Open Research Archives</collection><jtitle>Leukemia</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wang, D</au><au>Fløisand, Y</au><au>Myklebust, C V</au><au>Bürgler, S</au><au>Parente-Ribes, A</au><au>Hofgaard, P O</au><au>Bogen, B</au><au>Taskén, K</au><au>Tjønnfjord, G E</au><au>Schjesvold, F</au><au>Dalgaard, J</au><au>Tveita, A</au><au>Munthe, L A</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Autologous bone marrow Th cells can support multiple myeloma cell proliferation in vitro and in xenografted mice</atitle><jtitle>Leukemia</jtitle><stitle>Leukemia</stitle><addtitle>Leukemia</addtitle><date>2017-10-01</date><risdate>2017</risdate><volume>31</volume><issue>10</issue><spage>2114</spage><epage>2121</epage><pages>2114-2121</pages><issn>0887-6924</issn><eissn>1476-5551</eissn><abstract>Multiple myeloma (MM) is a plasma cell malignancy where MM cell growth is supported by the bone marrow (BM) microenvironment with poorly defined cellular and molecular mechanisms. MM cells express CD40, a receptor known to activate autocrine secretion of cytokines and elicit proliferation. Activated T helper (Th) cells express CD40 ligand (CD40L) and BM Th cells are significantly increased in MM patients. We hypothesized that activated BM Th cells could support MM cell growth. We here found that activated autologous BM Th cells supported MM cell growth in a contact- and CD40L-dependent manner
in vitro.
MM cells had retained the ability to activate Th cells that reciprocated and stimulated MM cell proliferation. Autologous BM Th cells supported MM cell growth in xenografted mice and were found in close contact with MM cells. MM cells secreted chemokines that attracted Th cells, secretion was augmented by CD40-stimulation. Within 14 days of culture of whole BM aspirates in autologous serum, MM cells and Th cells mutually stimulated each other, and MM cells required Th cells for further expansion
in vitro
and in mice. The results suggest that Th cells may support the expansion of MM cells in patients.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>28232741</pmid><doi>10.1038/leu.2017.69</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
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subjects | 631/67 631/67/1990/804 Aged Animals Antigen Presentation Autocrine signalling Autografts Bone marrow Bone Marrow Transplantation - adverse effects Cancer Research Care and treatment CD40 antigen CD40 Antigens - immunology CD40 Ligand - immunology CD40L protein Cell culture Cell Division Cell growth Cell proliferation Chemokines Chemokines - secretion Chemotaxis, Leukocyte Coculture Techniques Critical Care Medicine Cytokines Cytokines - secretion Development and progression Graft Survival - immunology Health aspects Helper cells Hematology Heterografts Humans Intensive Internal Medicine Lymphocyte Activation Lymphocytes T Malignancy Medicine Medicine & Public Health Mice Mice, Inbred NOD Mice, SCID Microenvironments Middle Aged Molecular modelling Multiple myeloma Multiple Myeloma - pathology Multiple Myeloma - secretion Multiple Myeloma - therapy Oncology original-article Patients T cells T-Lymphocytes, Helper-Inducer - immunology T-Lymphocytes, Helper-Inducer - transplantation Transplantation, Autologous - adverse effects Tumor Escape - immunology Tumor Microenvironment Xenografts |
title | Autologous bone marrow Th cells can support multiple myeloma cell proliferation in vitro and in xenografted mice |
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