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Immunotherapeutic effects of chitin in comparison with chitosan against Leishmania major infection
Institution:1. Department of Immunology, Faculty of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran;2. Department of Immunology, Pasteur Institute of Iran, Tehran, Iran;3. Department of Parasitology and Mycology, Faculty of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran;4. Department of Applied Cell Sciences, School of Advance Technologies in Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran;1. Department of Medical Parasitology & Mycology, School of Public Health, Tehran University of Medical Sciences, Tehran, Iran;2. Research Center for Endemic Parasites of Iran, Tehran University of Medical Sciences, Tehran, Iran;3. Isfahan Health Research Station, Tehran University of Medical Sciences, Tehran, Iran;4. Department of Medical Entomology and Vector Control,School of Public Health, Tehran University of Medical Sciences,Tehran Iran;5. Zoonoses Control Department, Center for Communicable Diseases Control, Ministry of Health and Medical Education, Tehran, Iran;6. Meshkin-Shahr Health Research Station, Tehran University of Medical Sciences, Tehran, Iran;7. Isfahan Province Health Center, Isfahan University of Medical Sciences, Isfahan, Iran;1. Instituto de Física, Universidade Federal de Goiás, Goiânia, GO, Brazil;2. Instituto Federal Goiano, Urutaí, GO, Brazil;3. Instituto de Física, Universidade de Brasília, Brasília, DF, Brazil;4. Instituto de Patologia Tropical e Saúde Publica, Departamento de Imunologia e Patologia Geral, Universidade Federal de Goiás, Goiânia, GO, Brazil
Abstract:Chitin and chitosan microparticles (MPs) are important immune system stimulators. The aim of this study was to evaluate the protective effects of these compounds in comparison with each other against Leishmania infection in BALB/c mice infected with Leishmania major (L. major).Female BALB/c mice were injected subcutaneously with 2 × 105 promastigotes. Chitin and/or chitosan MPs (< 40 μm) were subcutaneously injected in the BALB/c mice with two-day intervals until two weeks. Mice in all groups were sacrificed at 12 weeks post-infection. Enumeration of viable parasites was performed using limiting dilution assay. Furthermore, the animals (5 mice/group) were sacrificed two weeks post-infection. The lymph node cells were isolated and the effects of the chitinous MPs on the proliferation and production of cytokines such as tumor necrosis factor alpha (TNF-α) and interleukin-10 (IL-10) were determined. The mean sizes of lesions were significantly smaller in chitin (0.6 ± 0.12 mm) and chitosan treated groups (1.2 ± 0.8 mm) than in the control group (6.2 ± 1.7 mm) (P < 0.05). The parasite load in the lymph nodes of the treated mice was significantly lower than that in the lymph nodes of controls (1.31 × 106 vs 8.24 × 107 parasite/lymph node P = 0.032] and 7.49 × 106 vs 8.24 × 107 parasite/lymph node P = 0.05] for chitin and chitosan MPs treatment, respectively). We found that chitinous MPs induced cell proliferation and that chitin but not chitosan increased TNF-α and IL-10 production. Chitin appears that it has more effect than chitosan against leishmaniasis. The current study revealed that chitinous MPs had significant activity against L. major and could be considered as new therapeutic modality in leishmaniasis.
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