Cell-based therapy against prion diseases
•The available anti-prion drugs do not slow down prion disease progression in preclinical studies.•Adult neurogenesis is altered in prion disorders.•Cell-based therapeutic strategies can delay prion disease progression. Despite multiple efforts to find treatments, prion diseases are still incurable....
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Veröffentlicht in: | Current opinion in pharmacology 2019-02, Vol.44, p.8-14 |
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creator | Relaño-Ginés, Aroa Lehmann, Sylvain Crozet, Carole |
description | •The available anti-prion drugs do not slow down prion disease progression in preclinical studies.•Adult neurogenesis is altered in prion disorders.•Cell-based therapeutic strategies can delay prion disease progression.
Despite multiple efforts to find treatments, prion diseases are still incurable. The currently available therapeutic strategies are mostly based on compounds to inhibit pathological PrP (PrPSc) accumulation, and cellular PrP (PrPC) conversion into PrPSc. However, they cannot reverse the pathological changes already present in the brain. Cell-based therapeutic strategies could promote the repair of the pre-existing brain damage. The few available data come mostly from preclinical studies using neural stem cells, bone marrow-derived microglia and mesenchymal stem cells, as cell sources. Moreover, the benefits of cell-based therapeutic strategies could be linked not only to the replacement of damaged cells, but also to the secretion of trophic factors by the grafted cells that might modulate inflammation, cell death, or endogenous neurogenesis. |
doi_str_mv | 10.1016/j.coph.2018.11.001 |
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Despite multiple efforts to find treatments, prion diseases are still incurable. The currently available therapeutic strategies are mostly based on compounds to inhibit pathological PrP (PrPSc) accumulation, and cellular PrP (PrPC) conversion into PrPSc. However, they cannot reverse the pathological changes already present in the brain. Cell-based therapeutic strategies could promote the repair of the pre-existing brain damage. The few available data come mostly from preclinical studies using neural stem cells, bone marrow-derived microglia and mesenchymal stem cells, as cell sources. Moreover, the benefits of cell-based therapeutic strategies could be linked not only to the replacement of damaged cells, but also to the secretion of trophic factors by the grafted cells that might modulate inflammation, cell death, or endogenous neurogenesis.</description><identifier>ISSN: 1471-4892</identifier><identifier>EISSN: 1471-4973</identifier><identifier>DOI: 10.1016/j.coph.2018.11.001</identifier><identifier>PMID: 30472550</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><subject>Animals ; Human health and pathology ; Humans ; Life Sciences ; Mesenchymal Stem Cell Transplantation ; Microglia - transplantation ; Neural Stem Cells - transplantation ; Prion Diseases - therapy</subject><ispartof>Current opinion in pharmacology, 2019-02, Vol.44, p.8-14</ispartof><rights>2018</rights><rights>Copyright © 2018. Published by Elsevier Ltd.</rights><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c390t-d1ed285f44ce3be557cd69e5c91e3f95f2acbcbba0227917464b691f8116d14f3</citedby><cites>FETCH-LOGICAL-c390t-d1ed285f44ce3be557cd69e5c91e3f95f2acbcbba0227917464b691f8116d14f3</cites><orcidid>0000-0002-7292-7046 ; 0000-0001-6117-562X</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.coph.2018.11.001$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>230,314,776,780,881,3536,27903,27904,45974</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30472550$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://hal.umontpellier.fr/hal-02571397$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Relaño-Ginés, Aroa</creatorcontrib><creatorcontrib>Lehmann, Sylvain</creatorcontrib><creatorcontrib>Crozet, Carole</creatorcontrib><title>Cell-based therapy against prion diseases</title><title>Current opinion in pharmacology</title><addtitle>Curr Opin Pharmacol</addtitle><description>•The available anti-prion drugs do not slow down prion disease progression in preclinical studies.•Adult neurogenesis is altered in prion disorders.•Cell-based therapeutic strategies can delay prion disease progression.
Despite multiple efforts to find treatments, prion diseases are still incurable. The currently available therapeutic strategies are mostly based on compounds to inhibit pathological PrP (PrPSc) accumulation, and cellular PrP (PrPC) conversion into PrPSc. However, they cannot reverse the pathological changes already present in the brain. Cell-based therapeutic strategies could promote the repair of the pre-existing brain damage. The few available data come mostly from preclinical studies using neural stem cells, bone marrow-derived microglia and mesenchymal stem cells, as cell sources. Moreover, the benefits of cell-based therapeutic strategies could be linked not only to the replacement of damaged cells, but also to the secretion of trophic factors by the grafted cells that might modulate inflammation, cell death, or endogenous neurogenesis.</description><subject>Animals</subject><subject>Human health and pathology</subject><subject>Humans</subject><subject>Life Sciences</subject><subject>Mesenchymal Stem Cell Transplantation</subject><subject>Microglia - transplantation</subject><subject>Neural Stem Cells - transplantation</subject><subject>Prion Diseases - therapy</subject><issn>1471-4892</issn><issn>1471-4973</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kL1OwzAURi0EoqXwAgyoIx0SfO04jiUWVAFFqsQCs-XYN9RVmpQ4rdS3x1V_RiZb9vk-3XsIuQeaAoX8aZnadr1IGYUiBUgphQsyhExCkinJL0_3QrEBuQlhGQHBubwmA04zyYSgQzKZYl0npQnoxv0CO7Pejc2P8U3ox-vOt83Y-YDxO9ySq8rUAe-O54h8v71-TWfJ_PP9Y_oyTyxXtE8coGOFqLLMIi9RCGldrlBYBcgrJSpmbGnL0lDGpAKZ5VmZK6gKgNxBVvERmRx6F6bWcYSV6Xa6NV7PXuZ6_0aZkMCV3EJkHw_sumt_Nxh6vfLBxo1Mg-0maAa8oIIWgkaUHVDbtSF0WJ27geq9Tr3Ue516r1MD6Ggrhh6O_Ztyhe4cOfmLwPMBwGhk67HTwXpsLDrfoe21a_1__X-t44P7</recordid><startdate>201902</startdate><enddate>201902</enddate><creator>Relaño-Ginés, Aroa</creator><creator>Lehmann, Sylvain</creator><creator>Crozet, Carole</creator><general>Elsevier Ltd</general><general>Elsevier</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>7X8</scope><scope>1XC</scope><orcidid>https://orcid.org/0000-0002-7292-7046</orcidid><orcidid>https://orcid.org/0000-0001-6117-562X</orcidid></search><sort><creationdate>201902</creationdate><title>Cell-based therapy against prion diseases</title><author>Relaño-Ginés, Aroa ; Lehmann, Sylvain ; Crozet, Carole</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c390t-d1ed285f44ce3be557cd69e5c91e3f95f2acbcbba0227917464b691f8116d14f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Animals</topic><topic>Human health and pathology</topic><topic>Humans</topic><topic>Life Sciences</topic><topic>Mesenchymal Stem Cell Transplantation</topic><topic>Microglia - transplantation</topic><topic>Neural Stem Cells - transplantation</topic><topic>Prion Diseases - therapy</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Relaño-Ginés, Aroa</creatorcontrib><creatorcontrib>Lehmann, Sylvain</creatorcontrib><creatorcontrib>Crozet, Carole</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Hyper Article en Ligne (HAL)</collection><jtitle>Current opinion in pharmacology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Relaño-Ginés, Aroa</au><au>Lehmann, Sylvain</au><au>Crozet, Carole</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Cell-based therapy against prion diseases</atitle><jtitle>Current opinion in pharmacology</jtitle><addtitle>Curr Opin Pharmacol</addtitle><date>2019-02</date><risdate>2019</risdate><volume>44</volume><spage>8</spage><epage>14</epage><pages>8-14</pages><issn>1471-4892</issn><eissn>1471-4973</eissn><abstract>•The available anti-prion drugs do not slow down prion disease progression in preclinical studies.•Adult neurogenesis is altered in prion disorders.•Cell-based therapeutic strategies can delay prion disease progression.
Despite multiple efforts to find treatments, prion diseases are still incurable. The currently available therapeutic strategies are mostly based on compounds to inhibit pathological PrP (PrPSc) accumulation, and cellular PrP (PrPC) conversion into PrPSc. However, they cannot reverse the pathological changes already present in the brain. Cell-based therapeutic strategies could promote the repair of the pre-existing brain damage. The few available data come mostly from preclinical studies using neural stem cells, bone marrow-derived microglia and mesenchymal stem cells, as cell sources. Moreover, the benefits of cell-based therapeutic strategies could be linked not only to the replacement of damaged cells, but also to the secretion of trophic factors by the grafted cells that might modulate inflammation, cell death, or endogenous neurogenesis.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>30472550</pmid><doi>10.1016/j.coph.2018.11.001</doi><tpages>7</tpages><orcidid>https://orcid.org/0000-0002-7292-7046</orcidid><orcidid>https://orcid.org/0000-0001-6117-562X</orcidid></addata></record> |
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subjects | Animals Human health and pathology Humans Life Sciences Mesenchymal Stem Cell Transplantation Microglia - transplantation Neural Stem Cells - transplantation Prion Diseases - therapy |
title | Cell-based therapy against prion diseases |
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