In vitro model of postoncosphere development, and in vivo infection abilities of Taenia solium and Taenia saginata

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Taenia solium is known to cause human cysticercosis while T. saginata does not. Comparative in vitro and in vivo studies on the oncosphere and the postoncospheral (PO) forms of T. solium and T. saginata may help to elucidate why cysticercosis can occur from one and not the other. The aim of this stu...

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Detalles Bibliográficos
Autores: Palma S., Chile N., Carmen-Orozco R.P., Trompeter G., Fishbeck K., Cooper V., Rapoport L., Bernal-Teran E.G., Condori B.J., Gilman R.H., Verastegui M.R., for the Cysticercosis Working Group in Peru
Formato: artículo
Fecha de Publicación:2018
Institución:Consejo Nacional de Ciencia Tecnología e Innovación
Repositorio:CONCYTEC-Institucional
Lenguaje:inglés
OAI Identifier:oai:repositorio.concytec.gob.pe:20.500.12390/2776
Enlace del recurso:https://hdl.handle.net/20.500.12390/2776
https://doi.org/10.1371/journal.pntd.0007261
Nivel de acceso:acceso abierto
Materia:Public Health
Infectious Diseases
Environmental and Occupational Health
http://purl.org/pe-repo/ocde/ford#4.02.01
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dc.title.none.fl_str_mv In vitro model of postoncosphere development, and in vivo infection abilities of Taenia solium and Taenia saginata
title In vitro model of postoncosphere development, and in vivo infection abilities of Taenia solium and Taenia saginata
spellingShingle In vitro model of postoncosphere development, and in vivo infection abilities of Taenia solium and Taenia saginata
Palma S.
Public Health
Infectious Diseases
Environmental and Occupational Health
http://purl.org/pe-repo/ocde/ford#4.02.01
title_short In vitro model of postoncosphere development, and in vivo infection abilities of Taenia solium and Taenia saginata
title_full In vitro model of postoncosphere development, and in vivo infection abilities of Taenia solium and Taenia saginata
title_fullStr In vitro model of postoncosphere development, and in vivo infection abilities of Taenia solium and Taenia saginata
title_full_unstemmed In vitro model of postoncosphere development, and in vivo infection abilities of Taenia solium and Taenia saginata
title_sort In vitro model of postoncosphere development, and in vivo infection abilities of Taenia solium and Taenia saginata
author Palma S.
author_facet Palma S.
Chile N.
Carmen-Orozco R.P.
Trompeter G.
Fishbeck K.
Cooper V.
Rapoport L.
Bernal-Teran E.G.
Condori B.J.
Gilman R.H.
Verastegui M.R.
for the Cysticercosis Working Group in Peru
author_role author
author2 Chile N.
Carmen-Orozco R.P.
Trompeter G.
Fishbeck K.
Cooper V.
Rapoport L.
Bernal-Teran E.G.
Condori B.J.
Gilman R.H.
Verastegui M.R.
for the Cysticercosis Working Group in Peru
author2_role author
author
author
author
author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Palma S.
Chile N.
Carmen-Orozco R.P.
Trompeter G.
Fishbeck K.
Cooper V.
Rapoport L.
Bernal-Teran E.G.
Condori B.J.
Gilman R.H.
Verastegui M.R.
for the Cysticercosis Working Group in Peru
dc.subject.none.fl_str_mv Public Health
topic Public Health
Infectious Diseases
Environmental and Occupational Health
http://purl.org/pe-repo/ocde/ford#4.02.01
dc.subject.es_PE.fl_str_mv Infectious Diseases
Environmental and Occupational Health
dc.subject.ocde.none.fl_str_mv http://purl.org/pe-repo/ocde/ford#4.02.01
description Taenia solium is known to cause human cysticercosis while T. saginata does not. Comparative in vitro and in vivo studies on the oncosphere and the postoncospheral (PO) forms of T. solium and T. saginata may help to elucidate why cysticercosis can occur from one and not the other. The aim of this study was to use in vitro culture assays and in vivo models to study the differences in the development of the T. solium and T. saginata oncosphere. Furthermore, this study aimed to evaluate the expression of cytokines and metalloproteinases (MMPs) in human peripheral blood mononuclear cells (PBMCs), which were stimulated by these oncospheres and PO antigens. T. solium and T. saginata activated oncospheres (AO) were cultured in INT-407 and HCT-8 intestinal cells for 180 days. The T. solium began to die while the T. saginata grew for 180 days and developed to cysticerci in INT-407 cells. Rats were inoculated intracranially with AO and PO forms of either T. saginata or T. solium. Rats infected with T. solium AO and PO forms developed neurocysticercosis (NCC), while those infected with the T. saginata did not. Human PMBCs were stimulated with antigens of AO and PO forms of both species, and the production of cytokines and metalloproteinases (MMPs) was measured. The T. solium AO antigen stimulated a higher production of IL-4, IL-5, IL-13, IFN-γ, and IL-2 cytokines compared to T. saginata AO. In the PO form, the T. saginata PO antigen increased the production of IL-4, IL-5, IL-13, IFN-γ, IL-1β, IL-6, IL-10, TNF-α and IL-12 cytokines compared to T. solium, suggesting that this global immune response stimulated by different forms could permit survival or destruction of the parasite depending of their life-cycle stage. Regarding MMPs, T. solium AO antigen stimulated a higher production of MMP-9 compared to T. saginata AO antigen, which may be responsible for altering the permeability of intestinal cells and facilitating breakdown of the blood-brain barrier during the process of invasion of host tissue. © 2019 Palma et al.
publishDate 2018
dc.date.accessioned.none.fl_str_mv 2024-05-30T23:13:38Z
dc.date.available.none.fl_str_mv 2024-05-30T23:13:38Z
dc.date.issued.fl_str_mv 2018
dc.type.none.fl_str_mv info:eu-repo/semantics/article
format article
dc.identifier.uri.none.fl_str_mv https://hdl.handle.net/20.500.12390/2776
dc.identifier.doi.none.fl_str_mv https://doi.org/10.1371/journal.pntd.0007261
dc.identifier.scopus.none.fl_str_mv 2-s2.0-85063951711
url https://hdl.handle.net/20.500.12390/2776
https://doi.org/10.1371/journal.pntd.0007261
identifier_str_mv 2-s2.0-85063951711
dc.language.iso.none.fl_str_mv eng
language eng
dc.relation.ispartof.none.fl_str_mv PLoS Neglected Tropical Diseases
dc.rights.none.fl_str_mv info:eu-repo/semantics/openAccess
dc.rights.uri.none.fl_str_mv https://creativecommons.org/licenses/by/4.0/
eu_rights_str_mv openAccess
rights_invalid_str_mv https://creativecommons.org/licenses/by/4.0/
dc.publisher.none.fl_str_mv Public Library of Science
publisher.none.fl_str_mv Public Library of Science
dc.source.none.fl_str_mv reponame:CONCYTEC-Institucional
instname:Consejo Nacional de Ciencia Tecnología e Innovación
instacron:CONCYTEC
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instacron_str CONCYTEC
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collection CONCYTEC-Institucional
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spelling Publicationrp07415600rp07254600rp05664600rp05666600rp07416600rp07419600rp07418600rp07257600rp07414600rp00604600rp05775600rp07417600Palma S.Chile N.Carmen-Orozco R.P.Trompeter G.Fishbeck K.Cooper V.Rapoport L.Bernal-Teran E.G.Condori B.J.Gilman R.H.Verastegui M.R.for the Cysticercosis Working Group in Peru2024-05-30T23:13:38Z2024-05-30T23:13:38Z2018https://hdl.handle.net/20.500.12390/2776https://doi.org/10.1371/journal.pntd.00072612-s2.0-85063951711Taenia solium is known to cause human cysticercosis while T. saginata does not. Comparative in vitro and in vivo studies on the oncosphere and the postoncospheral (PO) forms of T. solium and T. saginata may help to elucidate why cysticercosis can occur from one and not the other. The aim of this study was to use in vitro culture assays and in vivo models to study the differences in the development of the T. solium and T. saginata oncosphere. Furthermore, this study aimed to evaluate the expression of cytokines and metalloproteinases (MMPs) in human peripheral blood mononuclear cells (PBMCs), which were stimulated by these oncospheres and PO antigens. T. solium and T. saginata activated oncospheres (AO) were cultured in INT-407 and HCT-8 intestinal cells for 180 days. The T. solium began to die while the T. saginata grew for 180 days and developed to cysticerci in INT-407 cells. Rats were inoculated intracranially with AO and PO forms of either T. saginata or T. solium. Rats infected with T. solium AO and PO forms developed neurocysticercosis (NCC), while those infected with the T. saginata did not. Human PMBCs were stimulated with antigens of AO and PO forms of both species, and the production of cytokines and metalloproteinases (MMPs) was measured. The T. solium AO antigen stimulated a higher production of IL-4, IL-5, IL-13, IFN-γ, and IL-2 cytokines compared to T. saginata AO. In the PO form, the T. saginata PO antigen increased the production of IL-4, IL-5, IL-13, IFN-γ, IL-1β, IL-6, IL-10, TNF-α and IL-12 cytokines compared to T. solium, suggesting that this global immune response stimulated by different forms could permit survival or destruction of the parasite depending of their life-cycle stage. Regarding MMPs, T. solium AO antigen stimulated a higher production of MMP-9 compared to T. saginata AO antigen, which may be responsible for altering the permeability of intestinal cells and facilitating breakdown of the blood-brain barrier during the process of invasion of host tissue. © 2019 Palma et al.Fondo Nacional de Desarrollo Científico y Tecnológico - FondecytengPublic Library of SciencePLoS Neglected Tropical Diseasesinfo:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by/4.0/Public HealthInfectious Diseases-1Environmental and Occupational Health-1http://purl.org/pe-repo/ocde/ford#4.02.01-1In vitro model of postoncosphere development, and in vivo infection abilities of Taenia solium and Taenia saginatainfo:eu-repo/semantics/articlereponame:CONCYTEC-Institucionalinstname:Consejo Nacional de Ciencia Tecnología e 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id="a30a8352-32d2-46b5-8e7d-63b05515e57e"> <Type xmlns="https://www.openaire.eu/cerif-profile/vocab/COAR_Publication_Types">http://purl.org/coar/resource_type/c_1843</Type> <Language>eng</Language> <Title>In vitro model of postoncosphere development, and in vivo infection abilities of Taenia solium and Taenia saginata</Title> <PublishedIn> <Publication> <Title>PLoS Neglected Tropical Diseases</Title> </Publication> </PublishedIn> <PublicationDate>2018</PublicationDate> <DOI>https://doi.org/10.1371/journal.pntd.0007261</DOI> <SCP-Number>2-s2.0-85063951711</SCP-Number> <Authors> <Author> <DisplayName>Palma S.</DisplayName> <Person id="rp07415" /> <Affiliation> <OrgUnit> </OrgUnit> </Affiliation> </Author> <Author> <DisplayName>Chile N.</DisplayName> <Person id="rp07254" /> <Affiliation> <OrgUnit> </OrgUnit> </Affiliation> </Author> <Author> <DisplayName>Carmen-Orozco R.P.</DisplayName> <Person id="rp05664" /> <Affiliation> <OrgUnit> </OrgUnit> </Affiliation> </Author> <Author> <DisplayName>Trompeter G.</DisplayName> <Person id="rp05666" /> <Affiliation> <OrgUnit> </OrgUnit> </Affiliation> </Author> <Author> <DisplayName>Fishbeck K.</DisplayName> <Person id="rp07416" /> <Affiliation> <OrgUnit> </OrgUnit> </Affiliation> </Author> <Author> <DisplayName>Cooper V.</DisplayName> <Person id="rp07419" /> <Affiliation> <OrgUnit> </OrgUnit> </Affiliation> </Author> <Author> <DisplayName>Rapoport L.</DisplayName> <Person id="rp07418" /> <Affiliation> <OrgUnit> </OrgUnit> </Affiliation> </Author> <Author> <DisplayName>Bernal-Teran E.G.</DisplayName> <Person id="rp07257" /> <Affiliation> <OrgUnit> </OrgUnit> </Affiliation> </Author> <Author> <DisplayName>Condori B.J.</DisplayName> <Person id="rp07414" /> <Affiliation> <OrgUnit> </OrgUnit> </Affiliation> </Author> <Author> <DisplayName>Gilman R.H.</DisplayName> <Person id="rp00604" /> <Affiliation> <OrgUnit> </OrgUnit> </Affiliation> </Author> <Author> <DisplayName>Verastegui M.R.</DisplayName> <Person id="rp05775" /> <Affiliation> <OrgUnit> </OrgUnit> </Affiliation> </Author> <Author> <DisplayName>for the Cysticercosis Working Group in Peru</DisplayName> <Person id="rp07417" /> <Affiliation> <OrgUnit> </OrgUnit> </Affiliation> </Author> </Authors> <Editors> </Editors> <Publishers> <Publisher> <DisplayName>Public Library of Science</DisplayName> <OrgUnit /> </Publisher> </Publishers> <License>https://creativecommons.org/licenses/by/4.0/</License> <Keyword>Public Health</Keyword> <Keyword>Infectious Diseases</Keyword> <Keyword>Environmental and Occupational Health</Keyword> <Abstract>Taenia solium is known to cause human cysticercosis while T. saginata does not. Comparative in vitro and in vivo studies on the oncosphere and the postoncospheral (PO) forms of T. solium and T. saginata may help to elucidate why cysticercosis can occur from one and not the other. The aim of this study was to use in vitro culture assays and in vivo models to study the differences in the development of the T. solium and T. saginata oncosphere. Furthermore, this study aimed to evaluate the expression of cytokines and metalloproteinases (MMPs) in human peripheral blood mononuclear cells (PBMCs), which were stimulated by these oncospheres and PO antigens. T. solium and T. saginata activated oncospheres (AO) were cultured in INT-407 and HCT-8 intestinal cells for 180 days. The T. solium began to die while the T. saginata grew for 180 days and developed to cysticerci in INT-407 cells. Rats were inoculated intracranially with AO and PO forms of either T. saginata or T. solium. Rats infected with T. solium AO and PO forms developed neurocysticercosis (NCC), while those infected with the T. saginata did not. Human PMBCs were stimulated with antigens of AO and PO forms of both species, and the production of cytokines and metalloproteinases (MMPs) was measured. The T. solium AO antigen stimulated a higher production of IL-4, IL-5, IL-13, IFN-γ, and IL-2 cytokines compared to T. saginata AO. In the PO form, the T. saginata PO antigen increased the production of IL-4, IL-5, IL-13, IFN-γ, IL-1β, IL-6, IL-10, TNF-α and IL-12 cytokines compared to T. solium, suggesting that this global immune response stimulated by different forms could permit survival or destruction of the parasite depending of their life-cycle stage. Regarding MMPs, T. solium AO antigen stimulated a higher production of MMP-9 compared to T. saginata AO antigen, which may be responsible for altering the permeability of intestinal cells and facilitating breakdown of the blood-brain barrier during the process of invasion of host tissue. © 2019 Palma et al.</Abstract> <Access xmlns="http://purl.org/coar/access_right" > </Access> </Publication> -1
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