Cytokine profile and nitric oxide levels in macrophages exposed to Leishmania infantum FML.
Animals
Chemokine CXCL10
/ metabolism
Cytokines
/ metabolism
Female
Interleukin-10
/ metabolism
Interleukin-12
/ metabolism
Lectins
/ pharmacology
Leishmania infantum
/ immunology
Macrophage Activation
Macrophages, Peritoneal
/ drug effects
Mice
Mice, Inbred BALB C
Nitric Oxide
/ metabolism
Tumor Necrosis Factor-alpha
/ metabolism
Fucose-mannose ligand
Macrophage
Nitric oxide
Visceral Leishmaniasis
Journal
Experimental parasitology
ISSN: 1090-2449
Titre abrégé: Exp Parasitol
Pays: United States
ID NLM: 0370713
Informations de publication
Date de publication:
Aug 2019
Aug 2019
Historique:
received:
03
04
2019
revised:
29
04
2019
accepted:
18
05
2019
pubmed:
28
5
2019
medline:
3
7
2019
entrez:
26
5
2019
Statut:
ppublish
Résumé
Fucose-mannose ligand (FML) is a soluble antigen purified from Leishmania donovani complex and used for diagnosis, prognosis, and vaccine development against visceral leishmaniasis (VL). We aimed to explore the effects of FML on the production of cytokines, chemokines and nitric oxide (NO) by macrophages in vitro. Peritoneal macrophages from BALB/c mice were treated with various concentrations of FML purified from Leishmania infantum in the absence or presence of LPS Peritoneal macrophages. After 48hr, cell culture supernatants were recovered and the levels of TNF-α, IL-10, IL-12p70 and IP-10 measured by Sandwich ELISA and NO concentration by Griess reaction. We found that FML significantly increase NO, IL-12p70 and IP-10 production in both LPS-treated and untreated macrophages and increase IL-10 levels only in LPS-treated macrophages. However, FML could not alert TNF-α levels in both LPS-treated and untreated macrophages. Further analysis revealed that FML can also increase IL-12p70/IL-10 ratio in LPS-treated macrophages. We concluded that FML can polarize macrophages to an appropriate phenotype similar to M1 phenotype against Leishmania donovani complex, although IL10 and TNF results are controversial.
Identifiants
pubmed: 31128104
pii: S0014-4894(19)30156-0
doi: 10.1016/j.exppara.2019.05.004
pii:
doi:
Substances chimiques
Chemokine CXCL10
0
Cxcl10 protein, mouse
0
Cytokines
0
Lectins
0
Tumor Necrosis Factor-alpha
0
fucose-binding lectin
0
Interleukin-10
130068-27-8
Interleukin-12
187348-17-0
Nitric Oxide
31C4KY9ESH
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
1-7Informations de copyright
Copyright © 2019. Published by Elsevier Inc.