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author Tavares, Grasiele S.V.
Mendonça, Débora V.C.
Pereira, Isabela A.G.
Oliveira-da-Silva, João A.
Ramos, Fernanda F.
Lage, Daniela P.
Machado, Amanda S.
Carvalho, Lívia M.
Reis, Thiago A.R.
Perin, Luísa
Carvalho, Ana Maria R.S.
Ottoni, Flaviano M.
Ludolf, Fernanda
Freitas, Camila S.
Bandeira, Raquel S.
Silva, Alessandra M.
Chávez-Fumagalli, Miguel A.
Duarte, Mariana C.
Menezes-Souza, Daniel
Alves, Ricardo J.
Roatt, Bruno M.
Coelho, Eduardo A.F.
author_facet Tavares, Grasiele S.V.
Mendonça, Débora V.C.
Pereira, Isabela A.G.
Oliveira-da-Silva, João A.
Ramos, Fernanda F.
Lage, Daniela P.
Machado, Amanda S.
Carvalho, Lívia M.
Reis, Thiago A.R.
Perin, Luísa
Carvalho, Ana Maria R.S.
Ottoni, Flaviano M.
Ludolf, Fernanda
Freitas, Camila S.
Bandeira, Raquel S.
Silva, Alessandra M.
Chávez-Fumagalli, Miguel A.
Duarte, Mariana C.
Menezes-Souza, Daniel
Alves, Ricardo J.
Roatt, Bruno M.
Coelho, Eduardo A.F.
contents Figure 3. Cellular profile generated in the treated and infected animals, 15 days after treatment. Fifteen days after treatment, cellular response was also evaluated in the treated and infected animals. Spleen cells (5 × 106 per mL) were non-stimulated (medium) or stimulated with Leishmania infantum SLA (50 µg/mL) for 48 h at 37 °C in 5% CO2. IFN-γ, IL-4, IL-10, IL-12p70 and GM-CSF levels were measured in the cell supernatant by a capture ELISA (A). Nitrite production was also evaluated in the cell supernatant (B). The ratios between the IFN-γ and IL-10 levels were calculated, and values are also shown (C). Bars represent the mean ± standard deviation of the groups. (*) indicates a statistically significant difference in relation to the saline and Mic/B groups (p <0.001). (+) indicates a statistically significant difference in relation to the miltefosine, ICHQ, and ICHQ/Mic groups (p <0.001).
format Recurso digital
id zenodo_https___doi_org_10_5281_zenodo_20217911
institution Zenodo
language
publishDate 2020
publisher Zenodo
record_format zenodo
spellingShingle Figure 3 in A clioquinol-containing Pluronic F127 polymeric micelle system is effective in the treatment of visceral leishmaniasis in a murine model
Tavares, Grasiele S.V.
Mendonça, Débora V.C.
Pereira, Isabela A.G.
Oliveira-da-Silva, João A.
Ramos, Fernanda F.
Lage, Daniela P.
Machado, Amanda S.
Carvalho, Lívia M.
Reis, Thiago A.R.
Perin, Luísa
Carvalho, Ana Maria R.S.
Ottoni, Flaviano M.
Ludolf, Fernanda
Freitas, Camila S.
Bandeira, Raquel S.
Silva, Alessandra M.
Chávez-Fumagalli, Miguel A.
Duarte, Mariana C.
Menezes-Souza, Daniel
Alves, Ricardo J.
Roatt, Bruno M.
Coelho, Eduardo A.F.
Biodiversity
Taxonomy
Figure 3. Cellular profile generated in the treated and infected animals, 15 days after treatment. Fifteen days after treatment, cellular response was also evaluated in the treated and infected animals. Spleen cells (5 × 106 per mL) were non-stimulated (medium) or stimulated with Leishmania infantum SLA (50 µg/mL) for 48 h at 37 °C in 5% CO2. IFN-γ, IL-4, IL-10, IL-12p70 and GM-CSF levels were measured in the cell supernatant by a capture ELISA (A). Nitrite production was also evaluated in the cell supernatant (B). The ratios between the IFN-γ and IL-10 levels were calculated, and values are also shown (C). Bars represent the mean ± standard deviation of the groups. (*) indicates a statistically significant difference in relation to the saline and Mic/B groups (p <0.001). (+) indicates a statistically significant difference in relation to the miltefosine, ICHQ, and ICHQ/Mic groups (p <0.001).
title Figure 3 in A clioquinol-containing Pluronic F127 polymeric micelle system is effective in the treatment of visceral leishmaniasis in a murine model
topic Biodiversity
Taxonomy
url https://doi.org/10.5281/zenodo.20217911