Immunomodulatory effects of chitin microparticles on Leishmania major-infected BALB/c mice

被引:18
作者
Ghotloo, Somayeh [1 ]
Hoseini, Mostafa Haji Molla [1 ,2 ]
Alimohammadian, Mohammad Hossein [3 ]
Khaze, Vahid [3 ]
Memarnejadian, Arash [4 ,5 ]
Rostami, Ali [6 ]
机构
[1] Shahid Beheshti Univ Med Sci, Fac Med, Dept Immunol, Tehran, Iran
[2] Shahid Beheshti Univ Med Sci, Sch Adv Technol Med, Dept Appl Cell Sci, Tehran, Iran
[3] Pasteur Inst Iran, Dept Immunol, Tehran, Iran
[4] Pasteur Inst Iran, Dept Hepatitis, Tehran, Iran
[5] Pasteur Inst Iran, AIDS, Tehran, Iran
[6] Shahid Beheshti Univ Med Sci, Sch Med, Dept Parasitol & Mycol, Tehran, Iran
关键词
Chitin microparticles; Leishmania major; Immunomodulation; Cytokine; INFLAMMATION; TISSUE; EOSINOPHILIA; IMMUNITY; TNF;
D O I
10.1016/j.parint.2014.12.007
中图分类号
R38 [医学寄生虫学]; Q [生物科学];
学科分类号
07 ; 0710 ; 09 ; 100103 ;
摘要
Chitin and its some derivatives are known to be non-allergic and non-toxic substances. It has been shown that chitin microparticles have immunomodulatory activities. In the present study, we investigated the in vivo immunomodulatory activities of chitin microparticles (CMPs) on Leishmania major-infected BALB/c mice. BALB/c mice were infected with L. major promastigotes at their base of the tail. CMPs (100 mu g/100 mu l) were injected into the site of infection from 3 days before to 2 or 8 weeks after infection at two-day intervals. Cytokine concentrations (TNF-alpha, IFN-gamma, IL-5 and IL-10) were measured using ELISA assays. Compared to the untreated group, production of TNF-alpha was significantly elevated in the CMPs-treated group. Moreover, the IFN-gamma/IL-5 ratio was significantly elevated in CMPs-treated infected mice (P = 0.023). Notably, the concentration of IL-10 was higher in CMPs-treated mice. These results showed that CMPs have in vivo immunomodulatory effects via the production of IFN-gamma and IL-10. We also measured the onset and size of lesions in both treated and untreated mice. The average times taken for the onset of the lesion formation were 35 and 29 days for CMPs-treated and untreated mice (P = 0.023), respectively. The mean size of the lesions was smaller in CMPs-treated group. Our study serves as a basis for future investigations on the application of CMPs as a prophylactic (vaccine adjuvant) and/or therapeutic modality against leishmaniasis. (C) 2014 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:219 / 221
页数:3
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