Loading…
Mesenchymal stromal cells and their derivatives – putative therapeutics in the management of autoimmune pancreatitis
Autoimmune pancreatitis, a derivative of chronic pancreatitis, frequently causes acute episodes with clinical symptoms parallel to those of acute pancreatitis. Corticosteroids are effective in the treatment of 90% of autoimmune pancreatitis cases, but for the remaining 10%, options are limited. Due...
Saved in:
Published in: | FEBS open bio 2020-06, Vol.10 (6), p.969-978 |
---|---|
Main Authors: | , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | cdi_FETCH-LOGICAL-c5626-6c7633fd9aaa6bbf497fbc3d2064d572932126921d1683e558fb71a1768449b33 |
---|---|
cites | cdi_FETCH-LOGICAL-c5626-6c7633fd9aaa6bbf497fbc3d2064d572932126921d1683e558fb71a1768449b33 |
container_end_page | 978 |
container_issue | 6 |
container_start_page | 969 |
container_title | FEBS open bio |
container_volume | 10 |
creator | Goodman, Robbie R. Davies, John E. |
description | Autoimmune pancreatitis, a derivative of chronic pancreatitis, frequently causes acute episodes with clinical symptoms parallel to those of acute pancreatitis. Corticosteroids are effective in the treatment of 90% of autoimmune pancreatitis cases, but for the remaining 10%, options are limited. Due to their significant immunomodulatory capabilities, mesenchymal stromal cells (MSCs) have been proposed as a novel treatment strategy for various immune and inflammatory pathologies including those with autoimmune origins. Here, we not only highlight the most recent MSC live‐cell experiments to address acute pancreatitis, but also discuss the opportunities afforded by the emergence of the newly identified field of MSC necrobiology. We conclude that the putative employment of MSC derivatives provides a newer and simpler therapeutic approach that could have significant advantages over the use of cells themselves.
Autoimmune pancreatitis frequently causes acute episodes with clinical symptoms parallel to those of acute pancreatitis. Due to their significant immunomodulatory capabilities, mesenchymal stromal cells (MSCs) have been proposed as a novel treatment strategy for various immune and inflammatory pathologies including those with autoimmune origins. Here, we not only highlight the most recent MSC live‐cell experiments to address acute pancreatitis, but also discuss the opportunities afforded by the emergence of the newly identified field of MSC necrobiology. |
doi_str_mv | 10.1002/2211-5463.12866 |
format | article |
fullrecord | <record><control><sourceid>proquest_doaj_</sourceid><recordid>TN_cdi_doaj_primary_oai_doaj_org_article_642627db6ca148d7936a197a11c8c02d</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><doaj_id>oai_doaj_org_article_642627db6ca148d7936a197a11c8c02d</doaj_id><sourcerecordid>2394261104</sourcerecordid><originalsourceid>FETCH-LOGICAL-c5626-6c7633fd9aaa6bbf497fbc3d2064d572932126921d1683e558fb71a1768449b33</originalsourceid><addsrcrecordid>eNqFks9u1DAQxiMEolXpmRuyxIXLtv4XO74gQdVCpSIucLYmtrPrVRIHO9lqb7wDb8iT4GzKquWCfbBn5pufxtZXFK8JviAY00tKCVmVXLALQishnhWnx8zzR_eT4jylLc5LYCIwflmcMJo3F_K02H1xyfVms--gRWmMYT6Na9uEoLdo3DgfkXXR72D0O5fQ75-_0DCNh2guRxjcNHqTkO_nGHXQw9p1rh9RaBBMY_BdN_UODdCb6HLj6NOr4kUDbXLnD-dZ8f3m-tvV59Xd10-3Vx_uVqYUVKyEkYKxxioAEHXdcCWb2jBLseC2lFQxSqhQlFgiKubKsmpqSYBIUXGuasbOituFawNs9RB9B3GvA3h9SIS41hDz9K3TglNBpa2FAcIrKxUTQJQEQkxlMLWZ9X5hDVPdOWvyCyO0T6BPK73f6HXYaZnBipQZ8O4BEMOPyaVRdz7Nfw29C1PSlKk8AyGYZ-nbf6TbMMU-f5WmHEulsCSz6nJRmRhSiq45DkOwni2iZxPo2QT6YJHc8ebxG476v4bIArEI7n3r9v_j6Zvrj3wh_wG4N8dq</addsrcrecordid><sourcetype>Open Website</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2407990714</pqid></control><display><type>article</type><title>Mesenchymal stromal cells and their derivatives – putative therapeutics in the management of autoimmune pancreatitis</title><source>Wiley-Blackwell Open Access Collection</source><source>Publicly Available Content Database</source><source>PubMed Central</source><creator>Goodman, Robbie R. ; Davies, John E.</creator><creatorcontrib>Goodman, Robbie R. ; Davies, John E.</creatorcontrib><description>Autoimmune pancreatitis, a derivative of chronic pancreatitis, frequently causes acute episodes with clinical symptoms parallel to those of acute pancreatitis. Corticosteroids are effective in the treatment of 90% of autoimmune pancreatitis cases, but for the remaining 10%, options are limited. Due to their significant immunomodulatory capabilities, mesenchymal stromal cells (MSCs) have been proposed as a novel treatment strategy for various immune and inflammatory pathologies including those with autoimmune origins. Here, we not only highlight the most recent MSC live‐cell experiments to address acute pancreatitis, but also discuss the opportunities afforded by the emergence of the newly identified field of MSC necrobiology. We conclude that the putative employment of MSC derivatives provides a newer and simpler therapeutic approach that could have significant advantages over the use of cells themselves.
Autoimmune pancreatitis frequently causes acute episodes with clinical symptoms parallel to those of acute pancreatitis. Due to their significant immunomodulatory capabilities, mesenchymal stromal cells (MSCs) have been proposed as a novel treatment strategy for various immune and inflammatory pathologies including those with autoimmune origins. Here, we not only highlight the most recent MSC live‐cell experiments to address acute pancreatitis, but also discuss the opportunities afforded by the emergence of the newly identified field of MSC necrobiology.</description><identifier>ISSN: 2211-5463</identifier><identifier>EISSN: 2211-5463</identifier><identifier>DOI: 10.1002/2211-5463.12866</identifier><identifier>PMID: 32323467</identifier><language>eng</language><publisher>England: John Wiley & Sons, Inc</publisher><subject>acute episodes ; anti‐inflammatory ; autoimmune pancreatitis ; Bone marrow ; Clinical trials ; Corticosteroids ; Cytokines ; Diabetes ; Disease ; Edema ; Genotype & phenotype ; Immunomodulation ; Inflammation ; Licenses ; Mesenchymal stem cells ; mesenchymal stromal cells ; Mesenchyme ; MSC derivatives ; MSC necrobiology ; Pancreatitis ; Regulatory approval ; Review ; Stem cells ; Stromal cells ; Tumor necrosis factor-TNF ; Vascular endothelial growth factor</subject><ispartof>FEBS open bio, 2020-06, Vol.10 (6), p.969-978</ispartof><rights>2020 The Authors. Published by FEBS Press and John Wiley & Sons Ltd.</rights><rights>2020. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5626-6c7633fd9aaa6bbf497fbc3d2064d572932126921d1683e558fb71a1768449b33</citedby><cites>FETCH-LOGICAL-c5626-6c7633fd9aaa6bbf497fbc3d2064d572932126921d1683e558fb71a1768449b33</cites><orcidid>0000-0002-8733-0082</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2407990714/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2407990714?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,11562,25753,27924,27925,37012,37013,44590,46052,46476,53791,53793,75126</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32323467$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Goodman, Robbie R.</creatorcontrib><creatorcontrib>Davies, John E.</creatorcontrib><title>Mesenchymal stromal cells and their derivatives – putative therapeutics in the management of autoimmune pancreatitis</title><title>FEBS open bio</title><addtitle>FEBS Open Bio</addtitle><description>Autoimmune pancreatitis, a derivative of chronic pancreatitis, frequently causes acute episodes with clinical symptoms parallel to those of acute pancreatitis. Corticosteroids are effective in the treatment of 90% of autoimmune pancreatitis cases, but for the remaining 10%, options are limited. Due to their significant immunomodulatory capabilities, mesenchymal stromal cells (MSCs) have been proposed as a novel treatment strategy for various immune and inflammatory pathologies including those with autoimmune origins. Here, we not only highlight the most recent MSC live‐cell experiments to address acute pancreatitis, but also discuss the opportunities afforded by the emergence of the newly identified field of MSC necrobiology. We conclude that the putative employment of MSC derivatives provides a newer and simpler therapeutic approach that could have significant advantages over the use of cells themselves.
Autoimmune pancreatitis frequently causes acute episodes with clinical symptoms parallel to those of acute pancreatitis. Due to their significant immunomodulatory capabilities, mesenchymal stromal cells (MSCs) have been proposed as a novel treatment strategy for various immune and inflammatory pathologies including those with autoimmune origins. Here, we not only highlight the most recent MSC live‐cell experiments to address acute pancreatitis, but also discuss the opportunities afforded by the emergence of the newly identified field of MSC necrobiology.</description><subject>acute episodes</subject><subject>anti‐inflammatory</subject><subject>autoimmune pancreatitis</subject><subject>Bone marrow</subject><subject>Clinical trials</subject><subject>Corticosteroids</subject><subject>Cytokines</subject><subject>Diabetes</subject><subject>Disease</subject><subject>Edema</subject><subject>Genotype & phenotype</subject><subject>Immunomodulation</subject><subject>Inflammation</subject><subject>Licenses</subject><subject>Mesenchymal stem cells</subject><subject>mesenchymal stromal cells</subject><subject>Mesenchyme</subject><subject>MSC derivatives</subject><subject>MSC necrobiology</subject><subject>Pancreatitis</subject><subject>Regulatory approval</subject><subject>Review</subject><subject>Stem cells</subject><subject>Stromal cells</subject><subject>Tumor necrosis factor-TNF</subject><subject>Vascular endothelial growth factor</subject><issn>2211-5463</issn><issn>2211-5463</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>24P</sourceid><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNqFks9u1DAQxiMEolXpmRuyxIXLtv4XO74gQdVCpSIucLYmtrPrVRIHO9lqb7wDb8iT4GzKquWCfbBn5pufxtZXFK8JviAY00tKCVmVXLALQishnhWnx8zzR_eT4jylLc5LYCIwflmcMJo3F_K02H1xyfVms--gRWmMYT6Na9uEoLdo3DgfkXXR72D0O5fQ75-_0DCNh2guRxjcNHqTkO_nGHXQw9p1rh9RaBBMY_BdN_UODdCb6HLj6NOr4kUDbXLnD-dZ8f3m-tvV59Xd10-3Vx_uVqYUVKyEkYKxxioAEHXdcCWb2jBLseC2lFQxSqhQlFgiKubKsmpqSYBIUXGuasbOituFawNs9RB9B3GvA3h9SIS41hDz9K3TglNBpa2FAcIrKxUTQJQEQkxlMLWZ9X5hDVPdOWvyCyO0T6BPK73f6HXYaZnBipQZ8O4BEMOPyaVRdz7Nfw29C1PSlKk8AyGYZ-nbf6TbMMU-f5WmHEulsCSz6nJRmRhSiq45DkOwni2iZxPo2QT6YJHc8ebxG476v4bIArEI7n3r9v_j6Zvrj3wh_wG4N8dq</recordid><startdate>202006</startdate><enddate>202006</enddate><creator>Goodman, Robbie R.</creator><creator>Davies, John E.</creator><general>John Wiley & Sons, Inc</general><general>John Wiley and Sons Inc</general><general>Wiley</general><scope>24P</scope><scope>WIN</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>8FE</scope><scope>8FH</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>LK8</scope><scope>M7P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0002-8733-0082</orcidid></search><sort><creationdate>202006</creationdate><title>Mesenchymal stromal cells and their derivatives – putative therapeutics in the management of autoimmune pancreatitis</title><author>Goodman, Robbie R. ; Davies, John E.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5626-6c7633fd9aaa6bbf497fbc3d2064d572932126921d1683e558fb71a1768449b33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>acute episodes</topic><topic>anti‐inflammatory</topic><topic>autoimmune pancreatitis</topic><topic>Bone marrow</topic><topic>Clinical trials</topic><topic>Corticosteroids</topic><topic>Cytokines</topic><topic>Diabetes</topic><topic>Disease</topic><topic>Edema</topic><topic>Genotype & phenotype</topic><topic>Immunomodulation</topic><topic>Inflammation</topic><topic>Licenses</topic><topic>Mesenchymal stem cells</topic><topic>mesenchymal stromal cells</topic><topic>Mesenchyme</topic><topic>MSC derivatives</topic><topic>MSC necrobiology</topic><topic>Pancreatitis</topic><topic>Regulatory approval</topic><topic>Review</topic><topic>Stem cells</topic><topic>Stromal cells</topic><topic>Tumor necrosis factor-TNF</topic><topic>Vascular endothelial growth factor</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Goodman, Robbie R.</creatorcontrib><creatorcontrib>Davies, John E.</creatorcontrib><collection>Wiley-Blackwell Open Access Collection</collection><collection>Wiley-Blackwell Free Backfiles(OpenAccess)</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Biological Science Collection</collection><collection>Biological Science Database</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>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>FEBS open bio</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Goodman, Robbie R.</au><au>Davies, John E.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Mesenchymal stromal cells and their derivatives – putative therapeutics in the management of autoimmune pancreatitis</atitle><jtitle>FEBS open bio</jtitle><addtitle>FEBS Open Bio</addtitle><date>2020-06</date><risdate>2020</risdate><volume>10</volume><issue>6</issue><spage>969</spage><epage>978</epage><pages>969-978</pages><issn>2211-5463</issn><eissn>2211-5463</eissn><abstract>Autoimmune pancreatitis, a derivative of chronic pancreatitis, frequently causes acute episodes with clinical symptoms parallel to those of acute pancreatitis. Corticosteroids are effective in the treatment of 90% of autoimmune pancreatitis cases, but for the remaining 10%, options are limited. Due to their significant immunomodulatory capabilities, mesenchymal stromal cells (MSCs) have been proposed as a novel treatment strategy for various immune and inflammatory pathologies including those with autoimmune origins. Here, we not only highlight the most recent MSC live‐cell experiments to address acute pancreatitis, but also discuss the opportunities afforded by the emergence of the newly identified field of MSC necrobiology. We conclude that the putative employment of MSC derivatives provides a newer and simpler therapeutic approach that could have significant advantages over the use of cells themselves.
Autoimmune pancreatitis frequently causes acute episodes with clinical symptoms parallel to those of acute pancreatitis. Due to their significant immunomodulatory capabilities, mesenchymal stromal cells (MSCs) have been proposed as a novel treatment strategy for various immune and inflammatory pathologies including those with autoimmune origins. Here, we not only highlight the most recent MSC live‐cell experiments to address acute pancreatitis, but also discuss the opportunities afforded by the emergence of the newly identified field of MSC necrobiology.</abstract><cop>England</cop><pub>John Wiley & Sons, Inc</pub><pmid>32323467</pmid><doi>10.1002/2211-5463.12866</doi><tpages>10</tpages><orcidid>https://orcid.org/0000-0002-8733-0082</orcidid><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 2211-5463 |
ispartof | FEBS open bio, 2020-06, Vol.10 (6), p.969-978 |
issn | 2211-5463 2211-5463 |
language | eng |
recordid | cdi_doaj_primary_oai_doaj_org_article_642627db6ca148d7936a197a11c8c02d |
source | Wiley-Blackwell Open Access Collection; Publicly Available Content Database; PubMed Central |
subjects | acute episodes anti‐inflammatory autoimmune pancreatitis Bone marrow Clinical trials Corticosteroids Cytokines Diabetes Disease Edema Genotype & phenotype Immunomodulation Inflammation Licenses Mesenchymal stem cells mesenchymal stromal cells Mesenchyme MSC derivatives MSC necrobiology Pancreatitis Regulatory approval Review Stem cells Stromal cells Tumor necrosis factor-TNF Vascular endothelial growth factor |
title | Mesenchymal stromal cells and their derivatives – putative therapeutics in the management of autoimmune pancreatitis |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-29T18%3A39%3A18IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_doaj_&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Mesenchymal%20stromal%20cells%20and%20their%20derivatives%20%E2%80%93%20putative%20therapeutics%20in%20the%20management%20of%20autoimmune%20pancreatitis&rft.jtitle=FEBS%20open%20bio&rft.au=Goodman,%20Robbie%20R.&rft.date=2020-06&rft.volume=10&rft.issue=6&rft.spage=969&rft.epage=978&rft.pages=969-978&rft.issn=2211-5463&rft.eissn=2211-5463&rft_id=info:doi/10.1002/2211-5463.12866&rft_dat=%3Cproquest_doaj_%3E2394261104%3C/proquest_doaj_%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c5626-6c7633fd9aaa6bbf497fbc3d2064d572932126921d1683e558fb71a1768449b33%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2407990714&rft_id=info:pmid/32323467&rfr_iscdi=true |