Effect of partial depletion of CD25+ T cells on neurological deficit and tissue damage in acute cerebral ischemia rat models

ABSTRACT: Objective: To evaluate the role of regulatory T cells (Tregs) at late stages of stroke. Methods: Anti-CD25 antibody (or PBS as a control) was injected to reduce the pool of Tregs in Wistar rats; then, ischemia was induced transiently by middle cerebral artery occlusion during 60 min and re...

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Autores:
Rodríguez Perea, Ana Lucía
Gutiérrez Vargas, Johanna
Rojas López, Mauricio
Cardona Gómez, Gloria Patricia
Velilla Hernández, Paula Andrea
Tipo de recurso:
Article of investigation
Fecha de publicación:
2018
Institución:
Universidad de Antioquia
Repositorio:
Repositorio UdeA
Idioma:
eng
OAI Identifier:
oai:bibliotecadigital.udea.edu.co:10495/23062
Acceso en línea:
http://hdl.handle.net/10495/23062
Palabra clave:
Isquemia Encefálica
Brain Ischemia
Linfocitos T Reguladores
T-Lymphocytes, Regulatory
Linfocitos T
T-Lymphocytes
Transitory middle cerebral artery occlusion
Rat
Anti-CD25
Rights
openAccess
License
https://creativecommons.org/licenses/by-nc-sa/4.0/
id UDEA2_2f6519faf24b1dcd46a90601ebfdd3da
oai_identifier_str oai:bibliotecadigital.udea.edu.co:10495/23062
network_acronym_str UDEA2
network_name_str Repositorio UdeA
repository_id_str
dc.title.spa.fl_str_mv Effect of partial depletion of CD25+ T cells on neurological deficit and tissue damage in acute cerebral ischemia rat models
title Effect of partial depletion of CD25+ T cells on neurological deficit and tissue damage in acute cerebral ischemia rat models
spellingShingle Effect of partial depletion of CD25+ T cells on neurological deficit and tissue damage in acute cerebral ischemia rat models
Isquemia Encefálica
Brain Ischemia
Linfocitos T Reguladores
T-Lymphocytes, Regulatory
Linfocitos T
T-Lymphocytes
Transitory middle cerebral artery occlusion
Rat
Anti-CD25
title_short Effect of partial depletion of CD25+ T cells on neurological deficit and tissue damage in acute cerebral ischemia rat models
title_full Effect of partial depletion of CD25+ T cells on neurological deficit and tissue damage in acute cerebral ischemia rat models
title_fullStr Effect of partial depletion of CD25+ T cells on neurological deficit and tissue damage in acute cerebral ischemia rat models
title_full_unstemmed Effect of partial depletion of CD25+ T cells on neurological deficit and tissue damage in acute cerebral ischemia rat models
title_sort Effect of partial depletion of CD25+ T cells on neurological deficit and tissue damage in acute cerebral ischemia rat models
dc.creator.fl_str_mv Rodríguez Perea, Ana Lucía
Gutiérrez Vargas, Johanna
Rojas López, Mauricio
Cardona Gómez, Gloria Patricia
Velilla Hernández, Paula Andrea
dc.contributor.author.none.fl_str_mv Rodríguez Perea, Ana Lucía
Gutiérrez Vargas, Johanna
Rojas López, Mauricio
Cardona Gómez, Gloria Patricia
Velilla Hernández, Paula Andrea
dc.contributor.researchgroup.spa.fl_str_mv Bacterias y Cáncer
Grupo de Inmunología Celular e Inmunogenética
Grupo de Neurociencias de Antioquia
Inmunovirología
dc.subject.decs.none.fl_str_mv Isquemia Encefálica
Brain Ischemia
Linfocitos T Reguladores
T-Lymphocytes, Regulatory
Linfocitos T
T-Lymphocytes
topic Isquemia Encefálica
Brain Ischemia
Linfocitos T Reguladores
T-Lymphocytes, Regulatory
Linfocitos T
T-Lymphocytes
Transitory middle cerebral artery occlusion
Rat
Anti-CD25
dc.subject.proposal.spa.fl_str_mv Transitory middle cerebral artery occlusion
Rat
Anti-CD25
description ABSTRACT: Objective: To evaluate the role of regulatory T cells (Tregs) at late stages of stroke. Methods: Anti-CD25 antibody (or PBS as a control) was injected to reduce the pool of Tregs in Wistar rats; then, ischemia was induced transiently by middle cerebral artery occlusion during 60 min and reperfusion was allowed for 7 d. Then, Treg frequency was analyzed in peripheral blood, spleen and lymph nodes. Neurological score (0-6) and infarct volume were also determined. Results: Nine days after injection, the CD4+ CD25+ T cells were reduced by 70.4%, 44.8% and 57.9% in peripheral blood, spleen and lymph nodes, respectively compared to PBS-treated rats. In contrast, the reduction of CD4+ FOXP3+ T cells was lower in the same compartments (38.6%, 12.5%, and 29.5%, respectively). The strongest reduction of CD25+ CD4+ T cells was observed in those FOXP3-negative cells in blood, spleen and lymph nodes (77.8%, 52.8%, and 60.7%, respectively), most likely corresponding to activated T cells. Anti-CD25-treated transient middle cerebral artery occlusion rats had a lower neurological deficit and did not develop tissue damage compared with PBS-treated animals. Conclusions: These findings suggest that treatment with anti-CD25 in our model preferentially reduce the T cell population with an activated phenotype, rather than the Treg population, leading to neuroprotection by suppressing the pathogenic response of effector T cells.
publishDate 2018
dc.date.issued.none.fl_str_mv 2018
dc.date.accessioned.none.fl_str_mv 2021-10-09T17:54:43Z
dc.date.available.none.fl_str_mv 2021-10-09T17:54:43Z
dc.type.spa.fl_str_mv Artículo de investigación
dc.type.coar.spa.fl_str_mv http://purl.org/coar/resource_type/c_2df8fbb1
dc.type.redcol.spa.fl_str_mv https://purl.org/redcol/resource_type/ART
dc.type.coarversion.spa.fl_str_mv http://purl.org/coar/version/c_970fb48d4fbd8a85
dc.type.driver.spa.fl_str_mv info:eu-repo/semantics/article
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dc.identifier.issn.none.fl_str_mv 2221-6189
dc.identifier.uri.none.fl_str_mv http://hdl.handle.net/10495/23062
dc.identifier.doi.none.fl_str_mv 10.4103/2221-6189.248029
dc.identifier.eissn.none.fl_str_mv 2589-5516
identifier_str_mv 2221-6189
10.4103/2221-6189.248029
2589-5516
url http://hdl.handle.net/10495/23062
dc.language.iso.spa.fl_str_mv eng
language eng
dc.relation.ispartofjournalabbrev.spa.fl_str_mv J. Acute Dis.
dc.relation.citationendpage.spa.fl_str_mv 253
dc.relation.citationissue.spa.fl_str_mv 6
dc.relation.citationstartpage.spa.fl_str_mv 247
dc.relation.citationvolume.spa.fl_str_mv 7
dc.relation.ispartofjournal.spa.fl_str_mv Journal of Acute Disease
dc.rights.uri.spa.fl_str_mv https://creativecommons.org/licenses/by-nc-sa/4.0/
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eu_rights_str_mv openAccess
dc.format.extent.spa.fl_str_mv 7
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dc.publisher.spa.fl_str_mv Hainan Medical University
dc.publisher.place.spa.fl_str_mv Haikou, China
institution Universidad de Antioquia
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spelling Rodríguez Perea, Ana LucíaGutiérrez Vargas, JohannaRojas López, MauricioCardona Gómez, Gloria PatriciaVelilla Hernández, Paula AndreaBacterias y CáncerGrupo de Inmunología Celular e InmunogenéticaGrupo de Neurociencias de AntioquiaInmunovirología2021-10-09T17:54:43Z2021-10-09T17:54:43Z20182221-6189http://hdl.handle.net/10495/2306210.4103/2221-6189.2480292589-5516ABSTRACT: Objective: To evaluate the role of regulatory T cells (Tregs) at late stages of stroke. Methods: Anti-CD25 antibody (or PBS as a control) was injected to reduce the pool of Tregs in Wistar rats; then, ischemia was induced transiently by middle cerebral artery occlusion during 60 min and reperfusion was allowed for 7 d. Then, Treg frequency was analyzed in peripheral blood, spleen and lymph nodes. Neurological score (0-6) and infarct volume were also determined. Results: Nine days after injection, the CD4+ CD25+ T cells were reduced by 70.4%, 44.8% and 57.9% in peripheral blood, spleen and lymph nodes, respectively compared to PBS-treated rats. In contrast, the reduction of CD4+ FOXP3+ T cells was lower in the same compartments (38.6%, 12.5%, and 29.5%, respectively). The strongest reduction of CD25+ CD4+ T cells was observed in those FOXP3-negative cells in blood, spleen and lymph nodes (77.8%, 52.8%, and 60.7%, respectively), most likely corresponding to activated T cells. Anti-CD25-treated transient middle cerebral artery occlusion rats had a lower neurological deficit and did not develop tissue damage compared with PBS-treated animals. Conclusions: These findings suggest that treatment with anti-CD25 in our model preferentially reduce the T cell population with an activated phenotype, rather than the Treg population, leading to neuroprotection by suppressing the pathogenic response of effector T cells.COL0070457COL0012444COL0010744COL00086397application/pdfengHainan Medical UniversityHaikou, Chinahttps://creativecommons.org/licenses/by-nc-sa/4.0/http://creativecommons.org/licenses/by-nc-sa/2.5/co/info:eu-repo/semantics/openAccesshttp://purl.org/coar/access_right/c_abf2Effect of partial depletion of CD25+ T cells on neurological deficit and tissue damage in acute cerebral ischemia rat modelsArtículo de investigaciónhttp://purl.org/coar/resource_type/c_2df8fbb1https://purl.org/redcol/resource_type/ARThttp://purl.org/coar/version/c_970fb48d4fbd8a85info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionIsquemia EncefálicaBrain IschemiaLinfocitos T ReguladoresT-Lymphocytes, RegulatoryLinfocitos TT-LymphocytesTransitory middle cerebral artery occlusionRatAnti-CD25J. 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