Treatment with synthetic lipophilic tyrosyl ester controls Leishmania major infection by reducing parasite load in BALB/c mice

Autor: Fatma Z. Guerfali, Hanène Attia, Youssef Gargouri, Pablo A. Leon Martinez, Ghada Mkannez, Aymen Bali, Dhafer Laouini, Imen Aissa, Rabiaa M. Sghaier
Přispěvatelé: Laboratoire de Transmission, Contrôle et Immunobiologie des Infections - Laboratory of Transmission, Control and Immunobiology of Infection (LR11IPT02), Institut Pasteur de Tunis, Réseau International des Instituts Pasteur (RIIP)-Réseau International des Instituts Pasteur (RIIP), Université de Tunis El Manar (UTM), École Nationale d'Ingénieurs de Sfax | National School of Engineers of Sfax (ENIS), This work received financial support from the Tunisian Ministry of Higher Education and Scientific Research to the Transmission, Control and Immunobiology of Infections Laboratory (LR11IPT02, D. Laouini)., We thank Mr A. Marouani and Dr Z. Ben Lasfer (Animal Facilities of the Institut Pasteur de Tunis) for their help conducting this study. We are also grateful to Ms S. Amouri for her help and thankful to Dr K. Ben-Aissa (Washignton, USA) and Dr S. Gritli (Department of Oto-Rhino-Laryngology, Charles Nicolle Hospital, Tunis, Tunisia) for their critical reading and grammar corrections
Rok vydání: 2016
Předmět:
0301 basic medicine
[SDV]Life Sciences [q-bio]
Pharmacology
Parasite load
Mice
parasite load
0302 clinical medicine
MESH: Animals
Leishmania major
MESH: Th1 Cells/immunology
Mice
Inbred BALB C

MESH: Leishmaniasis
Cutaneous/drug therapy

MESH: Tyrosine/analogs & derivatives
3. Good health
[SDV.MP]Life Sciences [q-bio]/Microbiology and Parasitology
Infectious Diseases
030220 oncology & carcinogenesis
Cytokines
Leishmania infantum
Injections
Subcutaneous

lipophilic tyrosyl ester
Antiprotozoal Agents
MESH: Mice
Inbred BALB C

Leishmaniasis
Cutaneous

MESH: Antiprotozoal Agents/administration & dosage
MESH: Leishmania major/drug effects
Biology
BALB/c
03 medical and health sciences
Cutaneous leishmaniasis
In vivo
MESH: Tyrosine/pharmacology
medicine
Animals
Immunologic Factors
MESH: Mice
anti-leishmanial activity
MESH: Injections
Subcutaneous

Th1 Cells
biology.organism_classification
medicine.disease
Leishmania
In vitro
MESH: Parasite Load
MESH: Immunologic Factors/administration & dosage
Disease Models
Animal

030104 developmental biology
Immunology
Tyrosine
Animal Science and Zoology
Parasitology
MESH: Cytokines/metabolism
MESH: Disease Models
Animal
Zdroj: Parasitology
Parasitology, Cambridge University Press (CUP), 2016, 143 (12), pp.1615-1620. ⟨10.1017/S0031182016001086⟩
ISSN: 1469-8161
0031-1820
Popis: SUMMARYSynthesized lipophilic tyrosyl ester derivatives with increasing lipophilicity were effective against Leishmania (L.) major and Leishmania infantum species in vitro. These findings prompted us to test in vivo leishmanicidal properties of these molecules and their potential effect on the modulation of immune responses. The experimental BALB/c model of cutaneous leishmaniasis was used in this study. Mice were infected with L. major parasites and treated with three in vitro active tyrosyl esters derivatives.Among these tested tyrosylcaprate (TyC) compounds, only TyC10 exhibited an in vivo anti-leishmanial activity, when injected sub-cutaneously (s.c.). TyC10 treatment of L. major-infected BALB/c mice resulted in a decrease of lesion development and parasite load. TyC10 s.c. treatment of non-infected mice induced an imbalance in interferon γ/interleukin 4 (IFN-γ/IL-4) ratio cytokines towards a Th1 response. Our results indicate that TyC10 s.c. treatment improves lesions’ healing and parasite clearance and may act on the cytokine balance towards a Th1 protective response by decreasing IL-4 and increasing IFN-γ transcripts. TyC10 is worthy of further investigation to uncover its mechanism of action that could lead to consider this molecule as a potential drug candidate.
Databáze: OpenAIRE