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The Role of Heterotypic DENV-specific CD8(+) T Lymphocytes in an Immunocompetent Mouse Model of Secondary Dengue Virus Infection
Dengue is the most prevalent arthropod-borne viral disease worldwide and is caused by the four dengue virus serotypes (DENV-1-4). Sequential heterologous DENV infections can be associated with severe disease manifestations. Here, we present an immunocompetent mouse model of secondary DENV infection...
Autores principales: | , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5478214/ https://www.ncbi.nlm.nih.gov/pubmed/28483582 http://dx.doi.org/10.1016/j.ebiom.2017.04.033 |
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author | Talarico, Laura B. Batalle, Juan P. Byrne, Alana B. Brahamian, Jorge M. Ferretti, Adrián García, Ayelén G. Mauri, Aldana Simonetto, Carla Hijano, Diego R. Lawrence, Andrea Acosta, Patricio L. Caballero, Mauricio T. Paredes Rojas, Yésica Ibañez, Lorena I. Melendi, Guillermina A. Rey, Félix A. Damonte, Elsa B. Harris, Eva Polack, Fernando P. |
author_facet | Talarico, Laura B. Batalle, Juan P. Byrne, Alana B. Brahamian, Jorge M. Ferretti, Adrián García, Ayelén G. Mauri, Aldana Simonetto, Carla Hijano, Diego R. Lawrence, Andrea Acosta, Patricio L. Caballero, Mauricio T. Paredes Rojas, Yésica Ibañez, Lorena I. Melendi, Guillermina A. Rey, Félix A. Damonte, Elsa B. Harris, Eva Polack, Fernando P. |
author_sort | Talarico, Laura B. |
collection | PubMed |
description | Dengue is the most prevalent arthropod-borne viral disease worldwide and is caused by the four dengue virus serotypes (DENV-1-4). Sequential heterologous DENV infections can be associated with severe disease manifestations. Here, we present an immunocompetent mouse model of secondary DENV infection using non mouse-adapted DENV strains to investigate the pathogenesis of severe dengue disease. C57BL/6 mice infected sequentially with DENV-1 (strain Puerto Rico/94) and DENV-2 (strain Tonga/74) developed low platelet counts, internal hemorrhages, and increase of liver enzymes. Cross-reactive CD8(+) T lymphocytes were found to be necessary and sufficient for signs of severe disease by adoptively transferring of DENV-1-immune CD8(+) T lymphocytes before DENV-2 challenge. Disease signs were associated with production of tumor necrosis factor (TNF)-α and elevated cytotoxicity displayed by heterotypic anti-DENV-1 CD8(+) T lymphocytes. These findings highlight the critical role of heterotypic anti-DENV CD8(+) T lymphocytes in manifestations of severe dengue disease. |
format | Online Article Text |
id | pubmed-5478214 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-54782142017-06-26 The Role of Heterotypic DENV-specific CD8(+) T Lymphocytes in an Immunocompetent Mouse Model of Secondary Dengue Virus Infection Talarico, Laura B. Batalle, Juan P. Byrne, Alana B. Brahamian, Jorge M. Ferretti, Adrián García, Ayelén G. Mauri, Aldana Simonetto, Carla Hijano, Diego R. Lawrence, Andrea Acosta, Patricio L. Caballero, Mauricio T. Paredes Rojas, Yésica Ibañez, Lorena I. Melendi, Guillermina A. Rey, Félix A. Damonte, Elsa B. Harris, Eva Polack, Fernando P. EBioMedicine Research Paper Dengue is the most prevalent arthropod-borne viral disease worldwide and is caused by the four dengue virus serotypes (DENV-1-4). Sequential heterologous DENV infections can be associated with severe disease manifestations. Here, we present an immunocompetent mouse model of secondary DENV infection using non mouse-adapted DENV strains to investigate the pathogenesis of severe dengue disease. C57BL/6 mice infected sequentially with DENV-1 (strain Puerto Rico/94) and DENV-2 (strain Tonga/74) developed low platelet counts, internal hemorrhages, and increase of liver enzymes. Cross-reactive CD8(+) T lymphocytes were found to be necessary and sufficient for signs of severe disease by adoptively transferring of DENV-1-immune CD8(+) T lymphocytes before DENV-2 challenge. Disease signs were associated with production of tumor necrosis factor (TNF)-α and elevated cytotoxicity displayed by heterotypic anti-DENV-1 CD8(+) T lymphocytes. These findings highlight the critical role of heterotypic anti-DENV CD8(+) T lymphocytes in manifestations of severe dengue disease. Elsevier 2017-04-27 /pmc/articles/PMC5478214/ /pubmed/28483582 http://dx.doi.org/10.1016/j.ebiom.2017.04.033 Text en © 2017 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Research Paper Talarico, Laura B. Batalle, Juan P. Byrne, Alana B. Brahamian, Jorge M. Ferretti, Adrián García, Ayelén G. Mauri, Aldana Simonetto, Carla Hijano, Diego R. Lawrence, Andrea Acosta, Patricio L. Caballero, Mauricio T. Paredes Rojas, Yésica Ibañez, Lorena I. Melendi, Guillermina A. Rey, Félix A. Damonte, Elsa B. Harris, Eva Polack, Fernando P. The Role of Heterotypic DENV-specific CD8(+) T Lymphocytes in an Immunocompetent Mouse Model of Secondary Dengue Virus Infection |
title | The Role of Heterotypic DENV-specific CD8(+) T Lymphocytes in an Immunocompetent Mouse Model of Secondary Dengue Virus Infection |
title_full | The Role of Heterotypic DENV-specific CD8(+) T Lymphocytes in an Immunocompetent Mouse Model of Secondary Dengue Virus Infection |
title_fullStr | The Role of Heterotypic DENV-specific CD8(+) T Lymphocytes in an Immunocompetent Mouse Model of Secondary Dengue Virus Infection |
title_full_unstemmed | The Role of Heterotypic DENV-specific CD8(+) T Lymphocytes in an Immunocompetent Mouse Model of Secondary Dengue Virus Infection |
title_short | The Role of Heterotypic DENV-specific CD8(+) T Lymphocytes in an Immunocompetent Mouse Model of Secondary Dengue Virus Infection |
title_sort | role of heterotypic denv-specific cd8(+) t lymphocytes in an immunocompetent mouse model of secondary dengue virus infection |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5478214/ https://www.ncbi.nlm.nih.gov/pubmed/28483582 http://dx.doi.org/10.1016/j.ebiom.2017.04.033 |
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