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| Indexado |
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| DOI | 10.4161/VIRU.32225 | ||||
| Año | 2014 | ||||
| Tipo | revisión |
Citas Totales
Autores Afiliación Chile
Instituciones Chile
% Participación
Internacional
Autores
Afiliación Extranjera
Instituciones
Extranjeras
Globally, the human respiratory syncytial virus (hRSV) is the major cause of lower respiratory tract infections (LRTIs) in infants and children younger than 2 years old. Furthermore, the number of hospitalizations due to LRTIs has shown a sustained increase every year due to the lack of effective vaccines against hRSV. Thus, this virus remains as a major public health and economic burden worldwide. The lung pathology developed in hRSV-infected humans is characterized by an exacerbated inflammatory and Th2 immune response. In order to rationally design new vaccines and therapies against this virus, several studies have focused in elucidating the interactions between hRSV virulence factors and the host immune system. Here, we discuss the main features of hRSV biology, the processes involved in virus recognition by the immune system and the most relevant mechanisms used by this pathogen to avoid the antiviral host response.
| Ord. | Autor | Género | Institución - País |
|---|---|---|---|
| 1 | ESPINOZA-VELIZ, JANYRA ALEJANDRA | - |
Pontificia Universidad Católica de Chile - Chile
|
| 2 | BOHMWALD-PRIETO, KAREN | Mujer |
Pontificia Universidad Católica de Chile - Chile
|
| 3 | CESPEDES-FERNANDEZ, PAMELA | Hombre |
Pontificia Universidad Católica de Chile - Chile
|
| 4 | RIEDEL-SORIA, CLAUDIA ANDREA | Mujer |
Universidad Nacional Andrés Bello - Chile
|
| 5 | BUENO-RAMIREZ, SUSAN MARCELA | Mujer |
Pontificia Universidad Católica de Chile - Chile
INSERM - Francia Centre de Recherche en Transplantation et Immunologie - Francia Center for Research in Transplantation and Translational Immunology - Francia |
| 6 | KALERGIS-PARRA, ALEXIS MIKES | Hombre |
Pontificia Universidad Católica de Chile - Chile
INSERM - Francia Center for Research in Transplantation and Translational Immunology - Francia |
| Fuente |
|---|
| FONDECYT |
| ECOS |
| Fondo Nacional de Desarrollo Científico, Tecnológico y de Innovación Tecnológica |
| Fondo Nacional de Desarrollo CientÃfico, Tecnológico y de Innovación Tecnológica |
| Millennium Institute on Immunology and Immunotherapy from Chile |
| Conseil Régional des Pays de la Loire |
| Biomedical Research Consortium |
| ECOS France-Chile grant |
| La Region Pays de la Loire through the "Chaire d'excellence program" |
| Grant "Nouvelles Equipes-nouvelles thematiques" |
| Conseil Régional des Pays de la Loire |
| Agradecimiento |
|---|
| This work was supported by the Millennium Institute on Immunology and Immunotherapy from Chile (P09/016-F for AMK and SB), La Region Pays de la Loire through the "Chaire d'excellence program" for AMK and Grant "Nouvelles Equipes-nouvelles thematiques"(to AMK and SMB), the ECOS France-Chile grant, FONDECYT no 1070352, FONDECYT no 1050979, FONDECYT no 1040349, FONDECYT no 1100926, FONDECYT no 1110397, FONDECYT no 1131012, FONDECYT no 1140010, FONDECYT no 3140455 and the Biomedical Research Consortium CTU06. JAE and KB are CONICYT-Chile fellows. |
| This work was supported by the Millennium Institute on Immunology and Immunotherapy from Chile (P09/016-F for AMK and SB), La Région Pays de la Loire through the “Chaire d’excellence program” for AMK and Grant “Nouvelles Equipes-nouvelles thématiques”(to AMK and SMB), the ECOS France-Chile grant, FONDECYT no 1070352, FONDECYT no 1050979, FONDECYT no 1040349, FONDECYT no 1100926, FONDECYT no 1110397, FONDECYT no 1131012, FONDECYT no 1140010, FONDECYT no 3140455 and the Biomedical Research Consortium CTU06. JAE and KB are CONICYT-Chile fellows. |