Selenization of S. cerevisiae increases its protective potential in experimental autoimmune encephalomyelitis by triggering an intestinal immunomodulatory loop
Autor(a) principal: | |
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Data de Publicação: | 2020 |
Outros Autores: | , , , , , , , , , , |
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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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) |
repository.mail.fl_str_mv |
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1808128735603326976 |