Resistance to experimental autoimmune encephalomyelitis development in Lewis rats from a conventional animal facility
Autor(a) principal: | |
---|---|
Data de Publicação: | 2007 |
Outros Autores: | , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UNESP |
Texto Completo: | http://dx.doi.org/10.1590/S0074-02762007000800007 http://hdl.handle.net/11449/27219 |
Resumo: | Experimental autoimmune encephalomyelitis (EAE) is an inflammatory disease of the brain and spinal cord that is mediated by CD4+ T lymphocytes specific to myelin components. In this study we compared development of EAE in Lewis rats from two colonies, one kept in pathogen-free conditions (CEMIB colony) and the other (Botucatu colony) kept in a conventional animal facility. Female Lewis rats were immunized with 100 µl of an emulsion containing 50 µg of myelin, associated with incomplete Freund's adjuvant plus Mycobacterium butyricum. Animals were daily evaluated for clinical score and weight. CEMIB colony presented high EAE incidence with clinical scores that varied from three to four along with significant weight losses. A variable disease incidence was observed in the Botucatu colony with clinical scores not higher than one and no weight loss. Immunological and histopathological characteristics were also compared after 20 days of immunization. Significant amounts of IFN-gamma, TNF-alpha and IL-10 were induced by myelin in cultures from CEMIB animals but not from the Botucatu colony. Significantly higher levels of anti-myelin IgG1 were detected in the CEMIB colony. Clear histopathological differences were also found. Cervical spinal cord sections from CEMIB animals showed typical perivascular inflammatory foci whereas samples from the Botucatu colony showed a scanty inflammatory infiltration. Helminths were found in animals from Botucatu colony but not, as expected, in the CEMIB pathogen-free animals. As the animals maintained in a conventional animal facility developed a very discrete clinical, and histopathological EAE in comparison to the rats kept in pathogen-free conditions, we believe that environmental factors such as intestinal parasites could underlie this resistance to EAE development, supporting the applicability of the hygiene hypothesis to EAE. |
id |
UNSP_029f505560f9f9e7162775216904b5fd |
---|---|
oai_identifier_str |
oai:repositorio.unesp.br:11449/27219 |
network_acronym_str |
UNSP |
network_name_str |
Repositório Institucional da UNESP |
repository_id_str |
2946 |
spelling |
Resistance to experimental autoimmune encephalomyelitis development in Lewis rats from a conventional animal facilityexperimental autoimmune encephalomyelitisrats inbred LewiscytokinesExperimental autoimmune encephalomyelitis (EAE) is an inflammatory disease of the brain and spinal cord that is mediated by CD4+ T lymphocytes specific to myelin components. In this study we compared development of EAE in Lewis rats from two colonies, one kept in pathogen-free conditions (CEMIB colony) and the other (Botucatu colony) kept in a conventional animal facility. Female Lewis rats were immunized with 100 µl of an emulsion containing 50 µg of myelin, associated with incomplete Freund's adjuvant plus Mycobacterium butyricum. Animals were daily evaluated for clinical score and weight. CEMIB colony presented high EAE incidence with clinical scores that varied from three to four along with significant weight losses. A variable disease incidence was observed in the Botucatu colony with clinical scores not higher than one and no weight loss. Immunological and histopathological characteristics were also compared after 20 days of immunization. Significant amounts of IFN-gamma, TNF-alpha and IL-10 were induced by myelin in cultures from CEMIB animals but not from the Botucatu colony. Significantly higher levels of anti-myelin IgG1 were detected in the CEMIB colony. Clear histopathological differences were also found. Cervical spinal cord sections from CEMIB animals showed typical perivascular inflammatory foci whereas samples from the Botucatu colony showed a scanty inflammatory infiltration. Helminths were found in animals from Botucatu colony but not, as expected, in the CEMIB pathogen-free animals. As the animals maintained in a conventional animal facility developed a very discrete clinical, and histopathological EAE in comparison to the rats kept in pathogen-free conditions, we believe that environmental factors such as intestinal parasites could underlie this resistance to EAE development, supporting the applicability of the hygiene hypothesis to EAE.Universidade Estadual Paulista Departamento de Microbiologia e Imunologia Instituto de BiociênciasUniversidade Estadual Paulista Departamento de Microbiologia e Imunologia Instituto de BiociênciasInstituto Oswaldo Cruz, Ministério da SaúdeUniversidade Estadual Paulista (Unesp)Zorzella, Sofia Fernanda Gonçalves [UNESP]Seger, Juliana [UNESP]Martins, Douglas Rodrigues [UNESP]Pelizon, Ana Claudia [UNESP]Sartori, Alexandrina [UNESP]2014-05-20T15:09:26Z2014-05-20T15:09:26Z2007-12-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article931-936application/pdfhttp://dx.doi.org/10.1590/S0074-02762007000800007Memórias do Instituto Oswaldo Cruz. Instituto Oswaldo Cruz, Ministério da Saúde, v. 102, n. 8, p. 931-936, 2007.0074-0276http://hdl.handle.net/11449/2721910.1590/S0074-02762007000800007S0074-02762007000800007S0074-02762007000800007.pdf4977572416129527SciELOreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengMemórias do Instituto Oswaldo Cruz2.8331,172info:eu-repo/semantics/openAccess2023-10-20T06:09:15Zoai:repositorio.unesp.br:11449/27219Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-05T15:28:41.233515Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false |
dc.title.none.fl_str_mv |
Resistance to experimental autoimmune encephalomyelitis development in Lewis rats from a conventional animal facility |
title |
Resistance to experimental autoimmune encephalomyelitis development in Lewis rats from a conventional animal facility |
spellingShingle |
Resistance to experimental autoimmune encephalomyelitis development in Lewis rats from a conventional animal facility Zorzella, Sofia Fernanda Gonçalves [UNESP] experimental autoimmune encephalomyelitis rats inbred Lewis cytokines |
title_short |
Resistance to experimental autoimmune encephalomyelitis development in Lewis rats from a conventional animal facility |
title_full |
Resistance to experimental autoimmune encephalomyelitis development in Lewis rats from a conventional animal facility |
title_fullStr |
Resistance to experimental autoimmune encephalomyelitis development in Lewis rats from a conventional animal facility |
title_full_unstemmed |
Resistance to experimental autoimmune encephalomyelitis development in Lewis rats from a conventional animal facility |
title_sort |
Resistance to experimental autoimmune encephalomyelitis development in Lewis rats from a conventional animal facility |
author |
Zorzella, Sofia Fernanda Gonçalves [UNESP] |
author_facet |
Zorzella, Sofia Fernanda Gonçalves [UNESP] Seger, Juliana [UNESP] Martins, Douglas Rodrigues [UNESP] Pelizon, Ana Claudia [UNESP] Sartori, Alexandrina [UNESP] |
author_role |
author |
author2 |
Seger, Juliana [UNESP] Martins, Douglas Rodrigues [UNESP] Pelizon, Ana Claudia [UNESP] Sartori, Alexandrina [UNESP] |
author2_role |
author author author author |
dc.contributor.none.fl_str_mv |
Universidade Estadual Paulista (Unesp) |
dc.contributor.author.fl_str_mv |
Zorzella, Sofia Fernanda Gonçalves [UNESP] Seger, Juliana [UNESP] Martins, Douglas Rodrigues [UNESP] Pelizon, Ana Claudia [UNESP] Sartori, Alexandrina [UNESP] |
dc.subject.por.fl_str_mv |
experimental autoimmune encephalomyelitis rats inbred Lewis cytokines |
topic |
experimental autoimmune encephalomyelitis rats inbred Lewis cytokines |
description |
Experimental autoimmune encephalomyelitis (EAE) is an inflammatory disease of the brain and spinal cord that is mediated by CD4+ T lymphocytes specific to myelin components. In this study we compared development of EAE in Lewis rats from two colonies, one kept in pathogen-free conditions (CEMIB colony) and the other (Botucatu colony) kept in a conventional animal facility. Female Lewis rats were immunized with 100 µl of an emulsion containing 50 µg of myelin, associated with incomplete Freund's adjuvant plus Mycobacterium butyricum. Animals were daily evaluated for clinical score and weight. CEMIB colony presented high EAE incidence with clinical scores that varied from three to four along with significant weight losses. A variable disease incidence was observed in the Botucatu colony with clinical scores not higher than one and no weight loss. Immunological and histopathological characteristics were also compared after 20 days of immunization. Significant amounts of IFN-gamma, TNF-alpha and IL-10 were induced by myelin in cultures from CEMIB animals but not from the Botucatu colony. Significantly higher levels of anti-myelin IgG1 were detected in the CEMIB colony. Clear histopathological differences were also found. Cervical spinal cord sections from CEMIB animals showed typical perivascular inflammatory foci whereas samples from the Botucatu colony showed a scanty inflammatory infiltration. Helminths were found in animals from Botucatu colony but not, as expected, in the CEMIB pathogen-free animals. As the animals maintained in a conventional animal facility developed a very discrete clinical, and histopathological EAE in comparison to the rats kept in pathogen-free conditions, we believe that environmental factors such as intestinal parasites could underlie this resistance to EAE development, supporting the applicability of the hygiene hypothesis to EAE. |
publishDate |
2007 |
dc.date.none.fl_str_mv |
2007-12-01 2014-05-20T15:09:26Z 2014-05-20T15:09:26Z |
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/10.1590/S0074-02762007000800007 Memórias do Instituto Oswaldo Cruz. Instituto Oswaldo Cruz, Ministério da Saúde, v. 102, n. 8, p. 931-936, 2007. 0074-0276 http://hdl.handle.net/11449/27219 10.1590/S0074-02762007000800007 S0074-02762007000800007 S0074-02762007000800007.pdf 4977572416129527 |
url |
http://dx.doi.org/10.1590/S0074-02762007000800007 http://hdl.handle.net/11449/27219 |
identifier_str_mv |
Memórias do Instituto Oswaldo Cruz. Instituto Oswaldo Cruz, Ministério da Saúde, v. 102, n. 8, p. 931-936, 2007. 0074-0276 10.1590/S0074-02762007000800007 S0074-02762007000800007 S0074-02762007000800007.pdf 4977572416129527 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Memórias do Instituto Oswaldo Cruz 2.833 1,172 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
931-936 application/pdf |
dc.publisher.none.fl_str_mv |
Instituto Oswaldo Cruz, Ministério da Saúde |
publisher.none.fl_str_mv |
Instituto Oswaldo Cruz, Ministério da Saúde |
dc.source.none.fl_str_mv |
SciELO 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 |
|
_version_ |
1808128517977669632 |