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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Veröffentlicht in:Leukemia 2017-10, Vol.31 (10), p.2114-2121
Hauptverfasser: 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
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container_end_page 2121
container_issue 10
container_start_page 2114
container_title Leukemia
container_volume 31
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
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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. 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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. 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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 &amp; 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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. 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identifier ISSN: 0887-6924
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issn 0887-6924
1476-5551
language eng
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source MEDLINE; NORA - Norwegian Open Research Archives; Nature Journals Online; SpringerLink Journals - AutoHoldings
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
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-06T00%3A01%3A20IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_crist&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Autologous%20bone%20marrow%20Th%20cells%20can%20support%20multiple%20myeloma%20cell%20proliferation%20in%20vitro%20and%20in%20xenografted%20mice&rft.jtitle=Leukemia&rft.au=Wang,%20D&rft.date=2017-10-01&rft.volume=31&rft.issue=10&rft.spage=2114&rft.epage=2121&rft.pages=2114-2121&rft.issn=0887-6924&rft.eissn=1476-5551&rft_id=info:doi/10.1038/leu.2017.69&rft_dat=%3Cgale_crist%3EA507901067%3C/gale_crist%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1946274455&rft_id=info:pmid/28232741&rft_galeid=A507901067&rfr_iscdi=true