Role of cytokines, NO, and H2O2 on the immunopathology of Leptospirosis in genetically selected mice
Autor(a) principal: | |
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Data de Publicação: | 2005 |
Outros Autores: | , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UNESP |
Texto Completo: | http://dx.doi.org/10.1590/S1678-91992005000200009 http://hdl.handle.net/11449/211855 |
Resumo: | Immune response to leptospirosis is mainly humorally mediated, and involves opsonization of leptospires for phagocytosis by macrophages and neutrophils. However, some aspects are still unknown. For a more detailed analysis of the cellular immune response to leptospirosis infection, trials were carried out in order to determine the hydrogen peroxide and nitric oxide (H2O2 and NO) production stimulated or not by Interferon-gamma. The participation of some specific cytokines, such as Tumor Necrosis Factor-alpha (TNF-alpha); Interferon-gamma (IFN-gamma); Interleukin-6 (IL-6); and Interleukin-4 (IL-4), in the immunopathology of this infection was also investigated. For this purpose, we analyzed the supernatant from peritoneal macrophage cell culture and the splenic cells of mice genetically selected as High (H) and Low (L) antibody producers, and inbred Balb/c mice infected with Leptospira interrogans serovar icterohaemorrhagiae. The IL-6 production varied from release peaks to inhibition in H, L, and Balb/c mice. Similar behavior was observed for IL-4, produced only by H and Balb/c mice. The three strains presented constant and elevated production of TNF-alpha until day 14, suggesting its effective participation in the initial phase of the infection. Meanwhile, all the three strains presented a constant and irregular IFN-gamma production, with release peaks between the 7th and 14th days in L mice. The H and Balb/c mice strains presented a higher tendency to Th2 response pattern, whereas L mice tended towards Th1 response. |
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Role of cytokines, NO, and H2O2 on the immunopathology of Leptospirosis in genetically selected miceleptospirosiscytokinescellular immunityImmune response to leptospirosis is mainly humorally mediated, and involves opsonization of leptospires for phagocytosis by macrophages and neutrophils. However, some aspects are still unknown. For a more detailed analysis of the cellular immune response to leptospirosis infection, trials were carried out in order to determine the hydrogen peroxide and nitric oxide (H2O2 and NO) production stimulated or not by Interferon-gamma. The participation of some specific cytokines, such as Tumor Necrosis Factor-alpha (TNF-alpha); Interferon-gamma (IFN-gamma); Interleukin-6 (IL-6); and Interleukin-4 (IL-4), in the immunopathology of this infection was also investigated. For this purpose, we analyzed the supernatant from peritoneal macrophage cell culture and the splenic cells of mice genetically selected as High (H) and Low (L) antibody producers, and inbred Balb/c mice infected with Leptospira interrogans serovar icterohaemorrhagiae. The IL-6 production varied from release peaks to inhibition in H, L, and Balb/c mice. Similar behavior was observed for IL-4, produced only by H and Balb/c mice. The three strains presented constant and elevated production of TNF-alpha until day 14, suggesting its effective participation in the initial phase of the infection. Meanwhile, all the three strains presented a constant and irregular IFN-gamma production, with release peaks between the 7th and 14th days in L mice. The H and Balb/c mice strains presented a higher tendency to Th2 response pattern, whereas L mice tended towards Th1 response.Universidade Estadual Paulista, Department of Animal Health and ProductionUniversidade Estadual Paulista, Araçatuba School of DentistryUniversidade Estadual Paulista, Institute of BiosciencesUniversidade Estadual Paulista, Department of Animal Health and ProductionUniversidade Estadual Paulista, Araçatuba School of DentistryUniversidade Estadual Paulista, Institute of BiosciencesCentro de Estudos de Venenos e Animais PeçonhentosUniversidade Estadual Paulista (Unesp)Marinho, M. [UNESP]Langoni, H. [UNESP]Oliveira, S. L. [UNESP]Lima, V. M. F. [UNESP]Peiró, J. R. [UNESP]Perri, S. H. V. [UNESP]Carreira, R. [UNESP]2021-07-14T10:30:42Z2021-07-14T10:30:42Z2005-06info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article198-212application/pdfhttp://dx.doi.org/10.1590/S1678-91992005000200009Journal of Venomous Animals and Toxins including Tropical Diseases. Botucatu, SP, Brazil: Centro de Estudos de Venenos e Animais Peçonhentos, v. 11, n. 2, p. 198-212, 2005.1678-9199http://hdl.handle.net/11449/21185510.1590/S1678-91992005000200009S1678-91992005000200009S1678-91992005000200009.pdfSciELOreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengJournal of Venomous Animals and Toxins including Tropical Diseasesinfo:eu-repo/semantics/openAccess2023-12-31T06:16:18Zoai:repositorio.unesp.br:11449/211855Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-05T21:45:11.511274Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false |
dc.title.none.fl_str_mv |
Role of cytokines, NO, and H2O2 on the immunopathology of Leptospirosis in genetically selected mice |
title |
Role of cytokines, NO, and H2O2 on the immunopathology of Leptospirosis in genetically selected mice |
spellingShingle |
Role of cytokines, NO, and H2O2 on the immunopathology of Leptospirosis in genetically selected mice Marinho, M. [UNESP] leptospirosis cytokines cellular immunity |
title_short |
Role of cytokines, NO, and H2O2 on the immunopathology of Leptospirosis in genetically selected mice |
title_full |
Role of cytokines, NO, and H2O2 on the immunopathology of Leptospirosis in genetically selected mice |
title_fullStr |
Role of cytokines, NO, and H2O2 on the immunopathology of Leptospirosis in genetically selected mice |
title_full_unstemmed |
Role of cytokines, NO, and H2O2 on the immunopathology of Leptospirosis in genetically selected mice |
title_sort |
Role of cytokines, NO, and H2O2 on the immunopathology of Leptospirosis in genetically selected mice |
author |
Marinho, M. [UNESP] |
author_facet |
Marinho, M. [UNESP] Langoni, H. [UNESP] Oliveira, S. L. [UNESP] Lima, V. M. F. [UNESP] Peiró, J. R. [UNESP] Perri, S. H. V. [UNESP] Carreira, R. [UNESP] |
author_role |
author |
author2 |
Langoni, H. [UNESP] Oliveira, S. L. [UNESP] Lima, V. M. F. [UNESP] Peiró, J. R. [UNESP] Perri, S. H. V. [UNESP] Carreira, R. [UNESP] |
author2_role |
author author author author author author |
dc.contributor.none.fl_str_mv |
Universidade Estadual Paulista (Unesp) |
dc.contributor.author.fl_str_mv |
Marinho, M. [UNESP] Langoni, H. [UNESP] Oliveira, S. L. [UNESP] Lima, V. M. F. [UNESP] Peiró, J. R. [UNESP] Perri, S. H. V. [UNESP] Carreira, R. [UNESP] |
dc.subject.por.fl_str_mv |
leptospirosis cytokines cellular immunity |
topic |
leptospirosis cytokines cellular immunity |
description |
Immune response to leptospirosis is mainly humorally mediated, and involves opsonization of leptospires for phagocytosis by macrophages and neutrophils. However, some aspects are still unknown. For a more detailed analysis of the cellular immune response to leptospirosis infection, trials were carried out in order to determine the hydrogen peroxide and nitric oxide (H2O2 and NO) production stimulated or not by Interferon-gamma. The participation of some specific cytokines, such as Tumor Necrosis Factor-alpha (TNF-alpha); Interferon-gamma (IFN-gamma); Interleukin-6 (IL-6); and Interleukin-4 (IL-4), in the immunopathology of this infection was also investigated. For this purpose, we analyzed the supernatant from peritoneal macrophage cell culture and the splenic cells of mice genetically selected as High (H) and Low (L) antibody producers, and inbred Balb/c mice infected with Leptospira interrogans serovar icterohaemorrhagiae. The IL-6 production varied from release peaks to inhibition in H, L, and Balb/c mice. Similar behavior was observed for IL-4, produced only by H and Balb/c mice. The three strains presented constant and elevated production of TNF-alpha until day 14, suggesting its effective participation in the initial phase of the infection. Meanwhile, all the three strains presented a constant and irregular IFN-gamma production, with release peaks between the 7th and 14th days in L mice. The H and Balb/c mice strains presented a higher tendency to Th2 response pattern, whereas L mice tended towards Th1 response. |
publishDate |
2005 |
dc.date.none.fl_str_mv |
2005-06 2021-07-14T10:30:42Z 2021-07-14T10:30:42Z |
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/S1678-91992005000200009 Journal of Venomous Animals and Toxins including Tropical Diseases. Botucatu, SP, Brazil: Centro de Estudos de Venenos e Animais Peçonhentos, v. 11, n. 2, p. 198-212, 2005. 1678-9199 http://hdl.handle.net/11449/211855 10.1590/S1678-91992005000200009 S1678-91992005000200009 S1678-91992005000200009.pdf |
url |
http://dx.doi.org/10.1590/S1678-91992005000200009 http://hdl.handle.net/11449/211855 |
identifier_str_mv |
Journal of Venomous Animals and Toxins including Tropical Diseases. Botucatu, SP, Brazil: Centro de Estudos de Venenos e Animais Peçonhentos, v. 11, n. 2, p. 198-212, 2005. 1678-9199 10.1590/S1678-91992005000200009 S1678-91992005000200009 S1678-91992005000200009.pdf |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Journal of Venomous Animals and Toxins including Tropical Diseases |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
198-212 application/pdf |
dc.publisher.none.fl_str_mv |
Centro de Estudos de Venenos e Animais Peçonhentos |
publisher.none.fl_str_mv |
Centro de Estudos de Venenos e Animais Peçonhentos |
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_ |
1808129354412064768 |