Immunomodulatory role of Th17 pathway in experimental visceral leishmaniasis.
Animals
Biomarkers
Cricetinae
Cytokines
/ genetics
Disease Models, Animal
Disease Susceptibility
Gene Expression Regulation
Host-Parasite Interactions
/ immunology
Immunomodulation
Leishmania donovani
/ immunology
Leishmaniasis, Visceral
/ immunology
Lymphocyte Activation
/ immunology
Mice
Signal Transduction
Spleen
/ immunology
Th17 Cells
/ immunology
Amphotericin B
Cytokines
Immunotherapy
Leishmania donovani
Th17 pathway
Visceral leishmaniasis
Journal
Immunobiology
ISSN: 1878-3279
Titre abrégé: Immunobiology
Pays: Netherlands
ID NLM: 8002742
Informations de publication
Date de publication:
11 2021
11 2021
Historique:
received:
28
05
2021
revised:
23
09
2021
accepted:
14
10
2021
pubmed:
14
11
2021
medline:
15
3
2022
entrez:
13
11
2021
Statut:
ppublish
Résumé
Visceral leishmaniasis (VL) or Kala-azar is a vector borne protozoan infection caused by Leishmania donovani in the Indian subcontinent mainly India, Nepal and Bangladesh. It is a major public health problem in these countries mostly affecting the socio-economically poor population. Leishmaniasis ranks the third most important disease after malaria and filariasis but is still considered as one of the neglected tropical diseases of the world. For development of better therapeutic agents and effective vaccine against VL, there is a need to understand host immunological changes that play a vital role during course of infection. Therefore, we investigated the role of Th17 pathway in Balb/c mice during Leishmania donovani infection and treatment with amphotericin B. Mice were divided in four groups i.e. Control, Infected, Uninfected treated and Infected treated. The cytokine levels were estimated in the spleen of Balb/c mice on days 1, 3, 7, 14, 17, 21, 28, 35, 45 and 60 post infection and during course of treatment. The mRNA levels of the Th17 pathway during active Leishmania donovani infection and after treatment were determined by real time polymerase chain reaction (RT-PCR) and protein levels by flow cytometry and ELISA. Results of our study revealed that active infection was associated with low levels of Th17 cytokines IL-17, IL-22 and IL-23 and elevated levels of IL-6, IL-1β and TGF-β. Amphotericin B treatment restored production of pro-inflammatory cytokines IL-17 and IL-22. The levels of transcription factor RORγt were found to correlate with the levels of IL-17 during infection and also after chemotherapy whereas STAT3 levels were elevated during infection and vice versa after treatment. The findings of this study suggest that Th17 cytokines IL-17 and IL-22 are associated with protection against VL infection and development of any interventions or chemotherapeutic agents targeting Th17 pathway could be an important approach for VL treatment.
Identifiants
pubmed: 34773853
pii: S0171-2985(21)00096-6
doi: 10.1016/j.imbio.2021.152148
pii:
doi:
Substances chimiques
Biomarkers
0
Cytokines
0
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
152148Informations de copyright
Copyright © 2021 Elsevier GmbH. All rights reserved.