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Contrasting Inflammatory Responses in Severe and Non-severe Community-acquired Pneumonia

The objective of this study was to compare systemic and local cytokine profiles and neutrophil responses in patients with severe versus non-severe community-acquired pneumonia (CAP). Hospitalized patients with CAP were grouped according to the pneumonia severity index (PSI), as non-severe (PSI < ...

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Detalles Bibliográficos
Autores principales: Fernandez-Botran, Rafael, Uriarte, Silvia M., Arnold, Forest W., Rodriguez-Hernandez, Lisandra, Rane, Madhavi J., Peyrani, Paula, Wiemken, Timothy, Kelley, Robert, Uppatla, Srinivas, Cavallazzi, Rodrigo, Blasi, Francesco, Morlacchi, Letizia, Aliberti, Stefano, Jonsson, Colleen, Ramirez, Julio A., Bordon, Jose
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7087758/
https://www.ncbi.nlm.nih.gov/pubmed/24557760
http://dx.doi.org/10.1007/s10753-014-9840-2
Descripción
Sumario:The objective of this study was to compare systemic and local cytokine profiles and neutrophil responses in patients with severe versus non-severe community-acquired pneumonia (CAP). Hospitalized patients with CAP were grouped according to the pneumonia severity index (PSI), as non-severe (PSI < 91 points) or severe (PSI ≥ 91 points). Blood and sputum samples were collected upon admission. Compared to non-severe CAP patients, the severe CAP group showed higher plasma levels of pro- and anti-inflammatory cytokines but in contrast, lower sputum concentrations of pro-inflammatory cytokines. Blood neutrophil functional responses were elevated in CAP patients compared to healthy controls. However, neutrophils from severe CAP patients showed reduced respiratory burst activity compared to the non-severe group. Results indicate that patients with severe CAP fail to mount a robust local pro-inflammatory response but exhibit instead a more substantial systemic inflammatory response, suggesting that a key driver of CAP severity may be the ability of the patient to generate an optimal local inflammatory response. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s10753-014-9840-2) contains supplementary material, which is available to authorized users.