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| Campo DC | Valor | Lengua/Idioma |
|---|---|---|
| dc.contributor.author | Ferrara, Florencia | - |
| dc.contributor.author | Rial, Analía | - |
| dc.contributor.author | Suárez, Norma | - |
| dc.contributor.author | Chabalgoity, José Alejandro | - |
| dc.date.accessioned | 2026-05-12T16:05:06Z | - |
| dc.date.available | 2026-05-12T16:05:06Z | - |
| dc.date.issued | 2021 | - |
| dc.identifier.citation | FERRARA, F., RIAL, A., SUÁREZ, N., y otros. Polyvalent Bacterial Lysate Protects Against Pneumonia Independently of Neutrophils, IL-17A or Caspase-1 Activation. Front. Immunol [en línea] 2021, 12. DOI: 10.3389/fimmu.2021.562244 | es |
| dc.identifier.uri | https://hdl.handle.net/20.500.12008/54958 | - |
| dc.description.abstract | Polyvalent bacterial lysates have been in use for decades for prevention and treatment of respiratory infections with reported clinical benefits. However, besides claims of broad immune activation, the mode of action is still a matter of debate. The lysates, formulated with the main bacterial species involved in respiratory infections, are commonly prepared by chemical or mechanical disruption of bacterial cells, what is believed influences the biological activity of the product. Here, we prepared two polyvalent lysates with the same composition but different method of bacterial cell disruption and evaluated their biological activity in a comparative fashion. We found that both bacterial lysates induce NF-kB activation in a MyD88 dependent manner, suggesting they work as TLR agonists. Further, we found that a single intranasal dose of any of the two lysates, is sufficient to protect against pneumococcal pneumonia, suggesting that they exert similar biological activity. We have previously shown that protection against pneumococcal pneumonia can also be induced by prior S. pneumoniae sub lethal infection or therapeutic treatment with a TLR5 agonist. Protection in those cases depends on neutrophil recruitment to the lungs, and can be associated with increased local expression of IL-17A. Here, we show that bacterial lysates exert protection against pneumococcal pneumonia independently of neutrophils, IL-17A or Caspase-1/11 activation, suggesting the existence of redundant mechanisms of protection. Trypsin-treated lysates afford protection to the same extent, suggesting that just small peptides suffice to exert the protective effect or that the molecules responsible for the protective effect are not proteins. Understanding the mechanism of action of bacterial lysates and deciphering the active components shall allow redesigning them with more precisely defined formulations and expanding their range of action. | es |
| dc.description.sponsorship | Agencia Nacional de Investigación e Innovación (ANII) | es |
| dc.format.mimetype | application/pdf | es |
| dc.language.iso | en | es |
| dc.relation.ispartof | Front. Immunol. 12, 2021 | es |
| dc.rights | Las obras depositadas en el Repositorio se rigen por la Ordenanza de los Derechos de la Propiedad Intelectual de la Universidad de la República.(Res. Nº 91 de C.D.C. de 8/III/1994 – D.O. 7/IV/1994) y por la Ordenanza del Repositorio Abierto de la Universidad de la República (Res. Nº 16 de C.D.C. de 07/10/2014) | es |
| dc.subject | polyvalent bacterial lysate | es |
| dc.subject | respiratory tract infections | es |
| dc.subject | TLR stimulation | es |
| dc.subject | pneumonia | es |
| dc.subject | lungs | es |
| dc.subject | IL-17A | es |
| dc.subject | inflammasome | es |
| dc.title | Polyvalent Bacterial Lysate Protects Against Pneumonia Independently of Neutrophils, IL-17A or Caspase-1 Activation | es |
| dc.type | Artículo | es |
| dc.contributor.filiacion | Ferrara Florencia, Universidad de la República (Uruguay). Facultad de Medicina. Instituto de Higiene. Unidad Académica Desarrollo Biotecnológico | - |
| dc.contributor.filiacion | Rial Analía, Universidad de la República (Uruguay). Facultad de Medicina. Instituto de Higiene. Unidad Académica Desarrollo Biotecnológico | - |
| dc.contributor.filiacion | Suárez Norma, Universidad de la República (Uruguay). Facultad de Medicina. Instituto de Higiene. Unidad Académica Desarrollo Biotecnológico | - |
| dc.contributor.filiacion | Chabalgoity José Alejandro, Universidad de la República (Uruguay). Facultad de Medicina. Instituto de Higiene. Unidad Académica Desarrollo Biotecnológico | - |
| dc.rights.licence | Licencia Creative Commons Atribución (CC - By 4.0) | es |
| dc.identifier.doi | 10.3389/fimmu.2021.562244 | - |
| Aparece en las colecciones: | Artículos - Instituto de Higiene | |
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| Fichero | Descripción | Tamaño | Formato | ||
|---|---|---|---|---|---|
| Polyvalent Bacterial Lysate Protects Against Pneumonia Independently of Neutrophils, IL-17A or Caspase-1 Activation.pdf | Artículo original | 827,3 kB | Adobe PDF | Visualizar/Abrir |
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