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Campo DC | Valor | Lengua/Idioma |
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dc.creator | Vintiñi, Elisa Ofelia | - |
dc.creator | Medina, Marcela Susana | - |
dc.date | 2018-12-20T14:12:45Z | - |
dc.date | 2018-12-20T14:12:45Z | - |
dc.date | 2017-12 | - |
dc.date | 2018-12-05T14:46:16Z | - |
dc.date.accessioned | 2019-04-29T15:41:53Z | - |
dc.date.available | 2019-04-29T15:41:53Z | - |
dc.date.issued | 2017-12 | - |
dc.identifier | Vintiñi, Elisa Ofelia; Medina, Marcela Susana; Non-Viable Lactobacillus Casei Beneficially Modulates Poly I:C Immune Response in Co-Cultures of Human Cells; Shiraz Inst Cancer Res; Iranian Journal Of Immunology; 14; 4; 12-2017; 325-339 | - |
dc.identifier | 1735-1383 | - |
dc.identifier | http://hdl.handle.net/11336/66817 | - |
dc.identifier | 1735-367X | - |
dc.identifier | CONICET Digital | - |
dc.identifier | CONICET | - |
dc.identifier.uri | http://rodna.bn.gov.ar:8080/jspui/handle/bnmm/299813 | - |
dc.description | Background: Polyinosinic:polycytidylic acid (Poly-IC) has been used as a viralstimulus to mimic in vivo and in vitro infection induced by some viruses. Objective: To determine whether non-viable Lactobacillus casei CRL431 (LcM) can modulate the immune response induced by Poly I:C in co-culture models of peripheral blood mononuclear cells (PBMC) and A549 cells. Methods: T and NK cell activation was evaluated by flow cytometry and levels of TNF-α, IFN-γ, IL-10, IL-29, and IL-17 by ELISA. Cells in direct contact with A549 (PBMC-A549) and cells with no contact with it (PBMC//A549) were used for this purpose. PBMCs alone and both co-culture systems were stimulated for 24 h with the following stimuli: LPS (10 µg/ml), LcM (106 UFC/ml), Poly I:C (2 µg/ml), Poly I:C+LcM, and LcM (3 h)+Poly I:C. Moreover, unstimulated cells were used as a control. Results: Poly I:C and LcM (3 h)+Poly I:C in PBMC-A549 showed a significant increase in the percentage of CD8+ expression (p<0.05). All stimuli induced significant activation from T CD4+, CD8+ cells compared with unstimulated PBMCs in both co-culture cells system. However, activation percentages were higher in direct co-culture. Poly I:C induced a higher level of proinflammatoryTNF-α and IFN-γ cytokines as well as IL-17 and IL-29 with lower IL-10levels in both co-culture systems while LcM induced a beneficial pattern of cytokines that would regulate Poly I:C effect. Conclusion: This in vitro model allowed us to highlight the potential of LcM as a modulator of anti-viral immune response and suggest its potential use in formulations against RNA respiratory viruses. | - |
dc.description | Fil: Vintiñi, Elisa Ofelia. Universidad Nacional de Tucumán. Facultad de Agronomía y Zootecnia; Argentina | - |
dc.description | Fil: Medina, Marcela Susana. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Tucumán; Argentina. Universidad Nacional de Tucumán. Facultad de Bioquímica, Química y Farmacia; Argentina | - |
dc.format | application/pdf | - |
dc.format | application/pdf | - |
dc.language | eng | - |
dc.publisher | Shiraz Inst Cancer Res | - |
dc.relation | info:eu-repo/semantics/altIdentifier/url/http://iji.sums.ac.ir/article_39328_f12863523edece69a6bfabf6e8c2692e.pdf | - |
dc.rights | info:eu-repo/semantics/openAccess | - |
dc.rights | https://creativecommons.org/licenses/by-nc-sa/2.5/ar/ | - |
dc.source | reponame:CONICET Digital (CONICET) | - |
dc.source | instname:Consejo Nacional de Investigaciones Científicas y Técnicas | - |
dc.source | instacron:CONICET | - |
dc.source.uri | http://hdl.handle.net/11336/65252 | - |
dc.subject | Poly I.C | - |
dc.subject | ANTIVIRAL IMMUNE RESPONSE | - |
dc.subject | NON VIABLE LACTOBACILLUS | - |
dc.subject | PBMC/A549 | - |
dc.subject | Salud Ocupacional | - |
dc.subject | Ciencias de la Salud | - |
dc.subject | CIENCIAS MÉDICAS Y DE LA SALUD | - |
dc.title | Non-Viable Lactobacillus Casei Beneficially Modulates Poly I:C Immune Response in Co-Cultures of Human Cells | - |
dc.type | info:eu-repo/semantics/article | - |
dc.type | info:eu-repo/semantics/publishedVersion | - |
dc.type | info:ar-repo/semantics/articulo | - |
Aparece en las colecciones: | CONICET |
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