Importance of CD8 T cell-mediated immune response during intracellular parasitic infections and its implications for the development of effective vaccines

Detalhes bibliográficos
Autor(a) principal: Rodrigues, Mauricio Martins [UNIFESP]
Data de Publicação: 2003
Outros Autores: Boscardin, Silvia Beatriz [UNIFESP], Vasconcelos, Jose Ronnie Carvalho de [UNIFESP], Hiyane, Meire Ioshie [UNIFESP], Salay, Gerson [UNIFESP], Soares, Irene S.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNIFESP
Texto Completo: http://dx.doi.org/10.1590/S0001-37652003000400005
http://repositorio.unifesp.br/handle/11600/1942
Resumo: Obligatory intracellular parasites such as Plasmodium sp, Trypanosoma cruzi, Toxoplasma gondii and Leishmania sp are responsible for the infection of hundreds of millions of individuals every year. These parasites can deliver antigens to the host cell cytoplasm that are presented through MHC class I molecules to protective CD8 T cells. The in vivo priming conditions of specific CD8 T cells during natural infection are largely unknown and remain as an area that has been poorly explored. The antiparasitic mechanisms mediated by CD8 T cells include both interferon-g-dependent and -independent pathways. The fact that CD8 T cells are potent inhibitors of parasitic development prompted many investigators to explore whether induction of these T cells can be a feasible strategy for the development of effective subunit vaccines against these parasitic diseases. Studies performed on experimental models supported the hypothesis that CD8 T cells induced by recombinant viral vectors or DNA vaccines could serve as the basis for human vaccination. Regimens of immunization consisting of two different vectors (heterologous prime-boost) are much more efficient in terms of expansion of protective CD8 T lymphocytes than immunization with a single vector. The results obtained using experimental models have led to clinical vaccination trials that are currently underway.
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spelling Importance of CD8 T cell-mediated immune response during intracellular parasitic infections and its implications for the development of effective vaccinesCD8parasitesimmunityvaccineCD8parasitasimunidadevacinasObligatory intracellular parasites such as Plasmodium sp, Trypanosoma cruzi, Toxoplasma gondii and Leishmania sp are responsible for the infection of hundreds of millions of individuals every year. These parasites can deliver antigens to the host cell cytoplasm that are presented through MHC class I molecules to protective CD8 T cells. The in vivo priming conditions of specific CD8 T cells during natural infection are largely unknown and remain as an area that has been poorly explored. The antiparasitic mechanisms mediated by CD8 T cells include both interferon-g-dependent and -independent pathways. The fact that CD8 T cells are potent inhibitors of parasitic development prompted many investigators to explore whether induction of these T cells can be a feasible strategy for the development of effective subunit vaccines against these parasitic diseases. Studies performed on experimental models supported the hypothesis that CD8 T cells induced by recombinant viral vectors or DNA vaccines could serve as the basis for human vaccination. Regimens of immunization consisting of two different vectors (heterologous prime-boost) are much more efficient in terms of expansion of protective CD8 T lymphocytes than immunization with a single vector. The results obtained using experimental models have led to clinical vaccination trials that are currently underway.Parasitas intracelulares obrigatórios como Plasmodium sp, Trypanosoma cruzi, Toxoplasma gondii e Leishmania sp são responsáveis pela infecção de milhões de indivíduos a cada ano. Estes parasitas são capazes de liberar antígenos no citoplasma de células infectadas do hospedeiro que são apresentados por moléculas de MHC classe I para células T CD8 protetoras. As condições de estímulo in vivo destas células T CD8 específicas durante a infecção natural são pouco conhecidas e constituem uma área pouco explorada. Os mecanismos anti-parasitários mediados por células T CD8 incluem vias dependentes e independentes do interferon-g. O fato que células T CD8 são potentes inibidores do desenvolvimento parasitário levou diversos investigadores a explorarem se a indução destes linfócitos T poderia constituir uma estratégia factível para o desenvolvimento de vacinas efetivas contra estas doenças parasitárias. Estudos feitos em modelos experimentais suportam a hipótese que células T CD8 induzidas por vetores recombinantes virais ou vacinas de DNA podem servir de base para a vacinação humana. Regimes de imunização consistindo de dois vetores distintos (prime-boost heterólogo) são muito mais eficientes em termos da expansão de linfócitos T CD8 protetores do que a imunização com um único vetor. Os resultados obtidos usando modelos experimentais levaram a vacinações clínicas que estão atualmente em curso.Universidade Federal de São Paulo (UNIFESP) Escola Paulista de Medicina Departamento de Microbiologia, Imunologia e ParasitologiaUniversidade de São Paulo Faculdade de Ciências Farmacêuticas Departamento de Análises Clínicas e ToxicológicasUNIFESP, EPM, Depto. de Microbiologia, Imunologia e ParasitologiaSciELOFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)Academia Brasileira de CiênciasUniversidade Federal de São Paulo (UNIFESP)Universidade de São Paulo (USP)Rodrigues, Mauricio Martins [UNIFESP]Boscardin, Silvia Beatriz [UNIFESP]Vasconcelos, Jose Ronnie Carvalho de [UNIFESP]Hiyane, Meire Ioshie [UNIFESP]Salay, Gerson [UNIFESP]Soares, Irene S.2015-06-14T13:30:14Z2015-06-14T13:30:14Z2003-12-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersion443-468application/pdfhttp://dx.doi.org/10.1590/S0001-37652003000400005Anais da Academia Brasileira de Ciências. Academia Brasileira de Ciências, v. 75, n. 4, p. 443-468, 2003.10.1590/S0001-37652003000400005S0001-37652003000400005.pdf0001-3765S0001-37652003000400005http://repositorio.unifesp.br/handle/11600/1942engAnais da Academia Brasileira de Ciênciasinfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESP2024-07-29T08:54:43Zoai:repositorio.unifesp.br/:11600/1942Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestbiblioteca.csp@unifesp.bropendoar:34652024-07-29T08:54:43Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false
dc.title.none.fl_str_mv Importance of CD8 T cell-mediated immune response during intracellular parasitic infections and its implications for the development of effective vaccines
title Importance of CD8 T cell-mediated immune response during intracellular parasitic infections and its implications for the development of effective vaccines
spellingShingle Importance of CD8 T cell-mediated immune response during intracellular parasitic infections and its implications for the development of effective vaccines
Rodrigues, Mauricio Martins [UNIFESP]
CD8
parasites
immunity
vaccine
CD8
parasitas
imunidade
vacinas
title_short Importance of CD8 T cell-mediated immune response during intracellular parasitic infections and its implications for the development of effective vaccines
title_full Importance of CD8 T cell-mediated immune response during intracellular parasitic infections and its implications for the development of effective vaccines
title_fullStr Importance of CD8 T cell-mediated immune response during intracellular parasitic infections and its implications for the development of effective vaccines
title_full_unstemmed Importance of CD8 T cell-mediated immune response during intracellular parasitic infections and its implications for the development of effective vaccines
title_sort Importance of CD8 T cell-mediated immune response during intracellular parasitic infections and its implications for the development of effective vaccines
author Rodrigues, Mauricio Martins [UNIFESP]
author_facet Rodrigues, Mauricio Martins [UNIFESP]
Boscardin, Silvia Beatriz [UNIFESP]
Vasconcelos, Jose Ronnie Carvalho de [UNIFESP]
Hiyane, Meire Ioshie [UNIFESP]
Salay, Gerson [UNIFESP]
Soares, Irene S.
author_role author
author2 Boscardin, Silvia Beatriz [UNIFESP]
Vasconcelos, Jose Ronnie Carvalho de [UNIFESP]
Hiyane, Meire Ioshie [UNIFESP]
Salay, Gerson [UNIFESP]
Soares, Irene S.
author2_role author
author
author
author
author
dc.contributor.none.fl_str_mv Universidade Federal de São Paulo (UNIFESP)
Universidade de São Paulo (USP)
dc.contributor.author.fl_str_mv Rodrigues, Mauricio Martins [UNIFESP]
Boscardin, Silvia Beatriz [UNIFESP]
Vasconcelos, Jose Ronnie Carvalho de [UNIFESP]
Hiyane, Meire Ioshie [UNIFESP]
Salay, Gerson [UNIFESP]
Soares, Irene S.
dc.subject.por.fl_str_mv CD8
parasites
immunity
vaccine
CD8
parasitas
imunidade
vacinas
topic CD8
parasites
immunity
vaccine
CD8
parasitas
imunidade
vacinas
description Obligatory intracellular parasites such as Plasmodium sp, Trypanosoma cruzi, Toxoplasma gondii and Leishmania sp are responsible for the infection of hundreds of millions of individuals every year. These parasites can deliver antigens to the host cell cytoplasm that are presented through MHC class I molecules to protective CD8 T cells. The in vivo priming conditions of specific CD8 T cells during natural infection are largely unknown and remain as an area that has been poorly explored. The antiparasitic mechanisms mediated by CD8 T cells include both interferon-g-dependent and -independent pathways. The fact that CD8 T cells are potent inhibitors of parasitic development prompted many investigators to explore whether induction of these T cells can be a feasible strategy for the development of effective subunit vaccines against these parasitic diseases. Studies performed on experimental models supported the hypothesis that CD8 T cells induced by recombinant viral vectors or DNA vaccines could serve as the basis for human vaccination. Regimens of immunization consisting of two different vectors (heterologous prime-boost) are much more efficient in terms of expansion of protective CD8 T lymphocytes than immunization with a single vector. The results obtained using experimental models have led to clinical vaccination trials that are currently underway.
publishDate 2003
dc.date.none.fl_str_mv 2003-12-01
2015-06-14T13:30:14Z
2015-06-14T13:30:14Z
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://dx.doi.org/10.1590/S0001-37652003000400005
Anais da Academia Brasileira de Ciências. Academia Brasileira de Ciências, v. 75, n. 4, p. 443-468, 2003.
10.1590/S0001-37652003000400005
S0001-37652003000400005.pdf
0001-3765
S0001-37652003000400005
http://repositorio.unifesp.br/handle/11600/1942
url http://dx.doi.org/10.1590/S0001-37652003000400005
http://repositorio.unifesp.br/handle/11600/1942
identifier_str_mv Anais da Academia Brasileira de Ciências. Academia Brasileira de Ciências, v. 75, n. 4, p. 443-468, 2003.
10.1590/S0001-37652003000400005
S0001-37652003000400005.pdf
0001-3765
S0001-37652003000400005
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Anais da Academia Brasileira de Ciências
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 443-468
application/pdf
dc.publisher.none.fl_str_mv Academia Brasileira de Ciências
publisher.none.fl_str_mv Academia Brasileira de Ciências
dc.source.none.fl_str_mv reponame:Repositório Institucional da UNIFESP
instname:Universidade Federal de São Paulo (UNIFESP)
instacron:UNIFESP
instname_str Universidade Federal de São Paulo (UNIFESP)
instacron_str UNIFESP
institution UNIFESP
reponame_str Repositório Institucional da UNIFESP
collection Repositório Institucional da UNIFESP
repository.name.fl_str_mv Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)
repository.mail.fl_str_mv biblioteca.csp@unifesp.br
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