Systemic and compartmentalized immune response in canine visceral leishmaniasis.

Detalhes bibliográficos
Autor(a) principal: Reis, Alexandre Barbosa
Data de Publicação: 2009
Outros Autores: Martins Filho, Olindo Assis, Carvalho, Andréa Teixeira de, Giunchetti, Rodolfo Cordeiro, Carneiro, Cláudia Martins, Mayrink, Wilson, Tafuri, Washington Luiz, Oliveira, Rodrigo Corrêa de
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UFOP
Texto Completo: http://www.repositorio.ufop.br/handle/123456789/4275
https://doi.org/10.1016/j.vetimm.2008.10.307
Resumo: Human visceral leishmaniasis (VL) and canine visceral leishmaniasis (CVL) are the most important emerging diseases with high prevalence in Latin American countries and are mainly caused by Leishmania (L.) chagasi (Syn = L. infantum). CVL has a great impact on Brazilian public health because domestic dogs are the most important VL peri-domicile reservoirs in both urban and peri-urban areas. Our findings highlight the complexity of cellular immunological events related to the natural infection from dogs by L. chagasi, additionally correlating major peripheral blood phenotypic markers with clinical status and tissues parasite density. Our main results demonstrated that lower frequency ofcirculating B cells and monocytes are important markers of severe CVL, whereas increased levels of CD8+ lymphocytes appear to be the major phenotypic feature of asymptomatic disease. Determination of the isotypes patterns during CVL demonstrated thatasymptomatic dogs and those with low parasitism are associated with an increase of IgG1, while the symptomatic dogs and those with high parasitism are associated with an increase of IgG, IgG2, IgM, IgA and IgE immunoglobulins. Pioneer findings obtained by our group showed a correlation between clinical status of CVL with degree of tissue parasite density. This data demonstrated that asymptomatic dogs presented low parasitism while symptomatic dogs are associated with high parasite load in various tissues such as skin, bone marrow and spleen. We have also investigated the association between tissue parasitism and CVL clinical forms. Regardless of clinical status, skin and spleen are the major sites of high parasite density during ongoing CVL. Furthermore, we demonstrated that bone marrow and spleen parasite density are the most reliable parasitological markers to decode the clinical status of CVL. In this article, we have reviewed some aspectsof the histopathological and immunological events occurring in natural and experimentalL. chagasi/L. infantum infection, pointing out the main L. chagasi-parasitized tissue. Wehave discussed the importance of the association between parasite density, immunological/ histopathological aspects and clinical status of the CVL, their current applications, challenges for the future and potential opportunities in CVL research.
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spelling Reis, Alexandre BarbosaMartins Filho, Olindo AssisCarvalho, Andréa Teixeira deGiunchetti, Rodolfo CordeiroCarneiro, Cláudia MartinsMayrink, WilsonTafuri, Washington LuizOliveira, Rodrigo Corrêa de2015-01-20T15:10:56Z2015-01-20T15:10:56Z2009REIS, A. B. et al. Systemic and compartmentalized immune response in canine visceral leishmaniasis. Veterinary Immunology and Immunopathology, v. 128, p. 87-95, 2009. Disponível em: <http://www.sciencedirect.com/science/article/pii/S0165242708003929>. Acesso em: 15 ago. 2014.0165-2427http://www.repositorio.ufop.br/handle/123456789/4275https://doi.org/10.1016/j.vetimm.2008.10.307Human visceral leishmaniasis (VL) and canine visceral leishmaniasis (CVL) are the most important emerging diseases with high prevalence in Latin American countries and are mainly caused by Leishmania (L.) chagasi (Syn = L. infantum). CVL has a great impact on Brazilian public health because domestic dogs are the most important VL peri-domicile reservoirs in both urban and peri-urban areas. Our findings highlight the complexity of cellular immunological events related to the natural infection from dogs by L. chagasi, additionally correlating major peripheral blood phenotypic markers with clinical status and tissues parasite density. Our main results demonstrated that lower frequency ofcirculating B cells and monocytes are important markers of severe CVL, whereas increased levels of CD8+ lymphocytes appear to be the major phenotypic feature of asymptomatic disease. Determination of the isotypes patterns during CVL demonstrated thatasymptomatic dogs and those with low parasitism are associated with an increase of IgG1, while the symptomatic dogs and those with high parasitism are associated with an increase of IgG, IgG2, IgM, IgA and IgE immunoglobulins. Pioneer findings obtained by our group showed a correlation between clinical status of CVL with degree of tissue parasite density. This data demonstrated that asymptomatic dogs presented low parasitism while symptomatic dogs are associated with high parasite load in various tissues such as skin, bone marrow and spleen. We have also investigated the association between tissue parasitism and CVL clinical forms. Regardless of clinical status, skin and spleen are the major sites of high parasite density during ongoing CVL. Furthermore, we demonstrated that bone marrow and spleen parasite density are the most reliable parasitological markers to decode the clinical status of CVL. In this article, we have reviewed some aspectsof the histopathological and immunological events occurring in natural and experimentalL. chagasi/L. infantum infection, pointing out the main L. chagasi-parasitized tissue. Wehave discussed the importance of the association between parasite density, immunological/ histopathological aspects and clinical status of the CVL, their current applications, challenges for the future and potential opportunities in CVL research.Clinical statusCanine visceral leishmaniasisParasite statusParasite densityImmunophenotypingSystemic and compartmentalized immune response in canine visceral leishmaniasis.info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleO periódico Veterinary Immunology and Immunopathology concede permissão para depósito deste artigo no Repositório Institucional da UFOP. 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dc.title.pt_BR.fl_str_mv Systemic and compartmentalized immune response in canine visceral leishmaniasis.
title Systemic and compartmentalized immune response in canine visceral leishmaniasis.
spellingShingle Systemic and compartmentalized immune response in canine visceral leishmaniasis.
Reis, Alexandre Barbosa
Clinical status
Canine visceral leishmaniasis
Parasite status
Parasite density
Immunophenotyping
title_short Systemic and compartmentalized immune response in canine visceral leishmaniasis.
title_full Systemic and compartmentalized immune response in canine visceral leishmaniasis.
title_fullStr Systemic and compartmentalized immune response in canine visceral leishmaniasis.
title_full_unstemmed Systemic and compartmentalized immune response in canine visceral leishmaniasis.
title_sort Systemic and compartmentalized immune response in canine visceral leishmaniasis.
author Reis, Alexandre Barbosa
author_facet Reis, Alexandre Barbosa
Martins Filho, Olindo Assis
Carvalho, Andréa Teixeira de
Giunchetti, Rodolfo Cordeiro
Carneiro, Cláudia Martins
Mayrink, Wilson
Tafuri, Washington Luiz
Oliveira, Rodrigo Corrêa de
author_role author
author2 Martins Filho, Olindo Assis
Carvalho, Andréa Teixeira de
Giunchetti, Rodolfo Cordeiro
Carneiro, Cláudia Martins
Mayrink, Wilson
Tafuri, Washington Luiz
Oliveira, Rodrigo Corrêa de
author2_role author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Reis, Alexandre Barbosa
Martins Filho, Olindo Assis
Carvalho, Andréa Teixeira de
Giunchetti, Rodolfo Cordeiro
Carneiro, Cláudia Martins
Mayrink, Wilson
Tafuri, Washington Luiz
Oliveira, Rodrigo Corrêa de
dc.subject.por.fl_str_mv Clinical status
Canine visceral leishmaniasis
Parasite status
Parasite density
Immunophenotyping
topic Clinical status
Canine visceral leishmaniasis
Parasite status
Parasite density
Immunophenotyping
description Human visceral leishmaniasis (VL) and canine visceral leishmaniasis (CVL) are the most important emerging diseases with high prevalence in Latin American countries and are mainly caused by Leishmania (L.) chagasi (Syn = L. infantum). CVL has a great impact on Brazilian public health because domestic dogs are the most important VL peri-domicile reservoirs in both urban and peri-urban areas. Our findings highlight the complexity of cellular immunological events related to the natural infection from dogs by L. chagasi, additionally correlating major peripheral blood phenotypic markers with clinical status and tissues parasite density. Our main results demonstrated that lower frequency ofcirculating B cells and monocytes are important markers of severe CVL, whereas increased levels of CD8+ lymphocytes appear to be the major phenotypic feature of asymptomatic disease. Determination of the isotypes patterns during CVL demonstrated thatasymptomatic dogs and those with low parasitism are associated with an increase of IgG1, while the symptomatic dogs and those with high parasitism are associated with an increase of IgG, IgG2, IgM, IgA and IgE immunoglobulins. Pioneer findings obtained by our group showed a correlation between clinical status of CVL with degree of tissue parasite density. This data demonstrated that asymptomatic dogs presented low parasitism while symptomatic dogs are associated with high parasite load in various tissues such as skin, bone marrow and spleen. We have also investigated the association between tissue parasitism and CVL clinical forms. Regardless of clinical status, skin and spleen are the major sites of high parasite density during ongoing CVL. Furthermore, we demonstrated that bone marrow and spleen parasite density are the most reliable parasitological markers to decode the clinical status of CVL. In this article, we have reviewed some aspectsof the histopathological and immunological events occurring in natural and experimentalL. chagasi/L. infantum infection, pointing out the main L. chagasi-parasitized tissue. Wehave discussed the importance of the association between parasite density, immunological/ histopathological aspects and clinical status of the CVL, their current applications, challenges for the future and potential opportunities in CVL research.
publishDate 2009
dc.date.issued.fl_str_mv 2009
dc.date.accessioned.fl_str_mv 2015-01-20T15:10:56Z
dc.date.available.fl_str_mv 2015-01-20T15:10:56Z
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dc.identifier.citation.fl_str_mv REIS, A. B. et al. Systemic and compartmentalized immune response in canine visceral leishmaniasis. Veterinary Immunology and Immunopathology, v. 128, p. 87-95, 2009. Disponível em: <http://www.sciencedirect.com/science/article/pii/S0165242708003929>. Acesso em: 15 ago. 2014.
dc.identifier.uri.fl_str_mv http://www.repositorio.ufop.br/handle/123456789/4275
dc.identifier.issn.none.fl_str_mv 0165-2427
dc.identifier.doi.none.fl_str_mv https://doi.org/10.1016/j.vetimm.2008.10.307
identifier_str_mv REIS, A. B. et al. Systemic and compartmentalized immune response in canine visceral leishmaniasis. Veterinary Immunology and Immunopathology, v. 128, p. 87-95, 2009. Disponível em: <http://www.sciencedirect.com/science/article/pii/S0165242708003929>. Acesso em: 15 ago. 2014.
0165-2427
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https://doi.org/10.1016/j.vetimm.2008.10.307
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