Selenization of S. cerevisiae increases its protective potential in experimental autoimmune encephalomyelitis by triggering an intestinal immunomodulatory loop

Detalhes bibliográficos
Autor(a) principal: de Campos Fraga-Silva, Thais Fernanda [UNESP]
Data de Publicação: 2020
Outros Autores: Mimura, Luiza Ayumi Nishiyama [UNESP], de Oliveira, Larissa Ragozo Cardoso [UNESP], dos Santos Toledo, Juliana Helena [UNESP], Borim, Patrícia Aparecida [UNESP], Zorzella-Pezavento, Sofia Fernanda Gonçalvez [UNESP], Alonso, Diego Peres [UNESP], Ribolla, Paulo Eduardo Martins [UNESP], de Oliveira, Carlos Alberto Ferreira, da Fonseca, Denise Morais, Villablanca, Eduardo J., Sartori, Alexandrina [UNESP]
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.1038/s41598-020-79102-7
http://hdl.handle.net/11449/208246
Resumo: Multiple sclerosis is an autoimmune disease that affects the myelinated central nervous system (CNS) neurons and triggers physical and cognitive disabilities. Conventional therapy is based on disease-modifying drugs that control disease severity but can also be deleterious. Complementary medicines have been adopted and evidence indicates that yeast supplements can improve symptoms mainly by modulating the immune response. In this investigation, we evaluated the therapeutic potential of Saccharomyces cerevisiae and its selenized derivative (Selemax) in experimental autoimmune encephalomyelitis (EAE). Female C57BL/6 mice submitted to EAE induction were orally supplemented with these yeasts by gavage from day 0 to day 14 after EAE induction. Both supplements determined significant reduction in clinical signs concomitantly with diminished Th1 immune response in CNS, increased proportion of Foxp3+ lymphocytes in inguinal and mesenteric lymph nodes and increased microbiota diversity. However, Selemax was more effective clinically and immunologically; it reduced disease prevalence more sharply, increased the proportion of CD103+ dendritic cells expressing high levels of PD-L1 in mesenteric lymph nodes and reduced the intestinal inflammatory process more strongly than S. cerevisiae. These results suggest a clear gut-brain axis modulation by selenized S. cerevisiae and suggest their inclusion in clinical trials.
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spelling Selenization of S. cerevisiae increases its protective potential in experimental autoimmune encephalomyelitis by triggering an intestinal immunomodulatory loopMultiple sclerosis is an autoimmune disease that affects the myelinated central nervous system (CNS) neurons and triggers physical and cognitive disabilities. Conventional therapy is based on disease-modifying drugs that control disease severity but can also be deleterious. Complementary medicines have been adopted and evidence indicates that yeast supplements can improve symptoms mainly by modulating the immune response. In this investigation, we evaluated the therapeutic potential of Saccharomyces cerevisiae and its selenized derivative (Selemax) in experimental autoimmune encephalomyelitis (EAE). Female C57BL/6 mice submitted to EAE induction were orally supplemented with these yeasts by gavage from day 0 to day 14 after EAE induction. Both supplements determined significant reduction in clinical signs concomitantly with diminished Th1 immune response in CNS, increased proportion of Foxp3+ lymphocytes in inguinal and mesenteric lymph nodes and increased microbiota diversity. However, Selemax was more effective clinically and immunologically; it reduced disease prevalence more sharply, increased the proportion of CD103+ dendritic cells expressing high levels of PD-L1 in mesenteric lymph nodes and reduced the intestinal inflammatory process more strongly than S. cerevisiae. These results suggest a clear gut-brain axis modulation by selenized S. cerevisiae and suggest their inclusion in clinical trials.Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)Botucatu Medical School São Paulo State University (UNESP)Institute of Biosciences São Paulo State University (UNESP)Institute of Biotechnology (IBTEC) São Paulo State University (UNESP)Biorigin ZilorInstitute of Biomedical Sciences University of São Paulo (USP)Immunology and Allergy Unit Department of Medicine Solna Karolinska Institutet and University HospitalBotucatu Medical School São Paulo State University (UNESP)Institute of Biosciences São Paulo State University (UNESP)Institute of Biotechnology (IBTEC) São Paulo State University (UNESP)FAPESP: 2016/23317-8CNPq: 307269/2017-5CAPES: PNPD 039/2017Universidade Estadual Paulista (Unesp)ZilorUniversidade de São Paulo (USP)Karolinska Institutet and University Hospitalde Campos Fraga-Silva, Thais Fernanda [UNESP]Mimura, Luiza Ayumi Nishiyama [UNESP]de Oliveira, Larissa Ragozo Cardoso [UNESP]dos Santos Toledo, Juliana Helena [UNESP]Borim, Patrícia Aparecida [UNESP]Zorzella-Pezavento, Sofia Fernanda Gonçalvez [UNESP]Alonso, Diego Peres [UNESP]Ribolla, Paulo Eduardo Martins [UNESP]de Oliveira, Carlos Alberto Ferreirada Fonseca, Denise MoraisVillablanca, Eduardo J.Sartori, Alexandrina [UNESP]2021-06-25T11:08:59Z2021-06-25T11:08:59Z2020-12-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttp://dx.doi.org/10.1038/s41598-020-79102-7Scientific Reports, v. 10, n. 1, 2020.2045-2322http://hdl.handle.net/11449/20824610.1038/s41598-020-79102-72-s2.0-85097682496Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengScientific Reportsinfo:eu-repo/semantics/openAccess2021-10-23T18:56:55Zoai:repositorio.unesp.br:11449/208246Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-05T17:00:10.026966Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Selenization of S. cerevisiae increases its protective potential in experimental autoimmune encephalomyelitis by triggering an intestinal immunomodulatory loop
title Selenization of S. cerevisiae increases its protective potential in experimental autoimmune encephalomyelitis by triggering an intestinal immunomodulatory loop
spellingShingle Selenization of S. cerevisiae increases its protective potential in experimental autoimmune encephalomyelitis by triggering an intestinal immunomodulatory loop
de Campos Fraga-Silva, Thais Fernanda [UNESP]
title_short Selenization of S. cerevisiae increases its protective potential in experimental autoimmune encephalomyelitis by triggering an intestinal immunomodulatory loop
title_full Selenization of S. cerevisiae increases its protective potential in experimental autoimmune encephalomyelitis by triggering an intestinal immunomodulatory loop
title_fullStr Selenization of S. cerevisiae increases its protective potential in experimental autoimmune encephalomyelitis by triggering an intestinal immunomodulatory loop
title_full_unstemmed Selenization of S. cerevisiae increases its protective potential in experimental autoimmune encephalomyelitis by triggering an intestinal immunomodulatory loop
title_sort Selenization of S. cerevisiae increases its protective potential in experimental autoimmune encephalomyelitis by triggering an intestinal immunomodulatory loop
author de Campos Fraga-Silva, Thais Fernanda [UNESP]
author_facet de Campos Fraga-Silva, Thais Fernanda [UNESP]
Mimura, Luiza Ayumi Nishiyama [UNESP]
de Oliveira, Larissa Ragozo Cardoso [UNESP]
dos Santos Toledo, Juliana Helena [UNESP]
Borim, Patrícia Aparecida [UNESP]
Zorzella-Pezavento, Sofia Fernanda Gonçalvez [UNESP]
Alonso, Diego Peres [UNESP]
Ribolla, Paulo Eduardo Martins [UNESP]
de Oliveira, Carlos Alberto Ferreira
da Fonseca, Denise Morais
Villablanca, Eduardo J.
Sartori, Alexandrina [UNESP]
author_role author
author2 Mimura, Luiza Ayumi Nishiyama [UNESP]
de Oliveira, Larissa Ragozo Cardoso [UNESP]
dos Santos Toledo, Juliana Helena [UNESP]
Borim, Patrícia Aparecida [UNESP]
Zorzella-Pezavento, Sofia Fernanda Gonçalvez [UNESP]
Alonso, Diego Peres [UNESP]
Ribolla, Paulo Eduardo Martins [UNESP]
de Oliveira, Carlos Alberto Ferreira
da Fonseca, Denise Morais
Villablanca, Eduardo J.
Sartori, Alexandrina [UNESP]
author2_role author
author
author
author
author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv Universidade Estadual Paulista (Unesp)
Zilor
Universidade de São Paulo (USP)
Karolinska Institutet and University Hospital
dc.contributor.author.fl_str_mv de Campos Fraga-Silva, Thais Fernanda [UNESP]
Mimura, Luiza Ayumi Nishiyama [UNESP]
de Oliveira, Larissa Ragozo Cardoso [UNESP]
dos Santos Toledo, Juliana Helena [UNESP]
Borim, Patrícia Aparecida [UNESP]
Zorzella-Pezavento, Sofia Fernanda Gonçalvez [UNESP]
Alonso, Diego Peres [UNESP]
Ribolla, Paulo Eduardo Martins [UNESP]
de Oliveira, Carlos Alberto Ferreira
da Fonseca, Denise Morais
Villablanca, Eduardo J.
Sartori, Alexandrina [UNESP]
description Multiple sclerosis is an autoimmune disease that affects the myelinated central nervous system (CNS) neurons and triggers physical and cognitive disabilities. Conventional therapy is based on disease-modifying drugs that control disease severity but can also be deleterious. Complementary medicines have been adopted and evidence indicates that yeast supplements can improve symptoms mainly by modulating the immune response. In this investigation, we evaluated the therapeutic potential of Saccharomyces cerevisiae and its selenized derivative (Selemax) in experimental autoimmune encephalomyelitis (EAE). Female C57BL/6 mice submitted to EAE induction were orally supplemented with these yeasts by gavage from day 0 to day 14 after EAE induction. Both supplements determined significant reduction in clinical signs concomitantly with diminished Th1 immune response in CNS, increased proportion of Foxp3+ lymphocytes in inguinal and mesenteric lymph nodes and increased microbiota diversity. However, Selemax was more effective clinically and immunologically; it reduced disease prevalence more sharply, increased the proportion of CD103+ dendritic cells expressing high levels of PD-L1 in mesenteric lymph nodes and reduced the intestinal inflammatory process more strongly than S. cerevisiae. These results suggest a clear gut-brain axis modulation by selenized S. cerevisiae and suggest their inclusion in clinical trials.
publishDate 2020
dc.date.none.fl_str_mv 2020-12-01
2021-06-25T11:08:59Z
2021-06-25T11:08:59Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://dx.doi.org/10.1038/s41598-020-79102-7
Scientific Reports, v. 10, n. 1, 2020.
2045-2322
http://hdl.handle.net/11449/208246
10.1038/s41598-020-79102-7
2-s2.0-85097682496
url http://dx.doi.org/10.1038/s41598-020-79102-7
http://hdl.handle.net/11449/208246
identifier_str_mv Scientific Reports, v. 10, n. 1, 2020.
2045-2322
10.1038/s41598-020-79102-7
2-s2.0-85097682496
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Scientific Reports
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.source.none.fl_str_mv Scopus
reponame:Repositório Institucional da UNESP
instname:Universidade Estadual Paulista (UNESP)
instacron:UNESP
instname_str Universidade Estadual Paulista (UNESP)
instacron_str UNESP
institution UNESP
reponame_str Repositório Institucional da UNESP
collection Repositório Institucional da UNESP
repository.name.fl_str_mv Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)
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