Generation of avirulent Leishmania parasites and induction of nitric oxide production in macrophages by using polyacrylic acid

被引:10
作者
Elcicek, Serhat [1 ]
Bagirova, Malahat [2 ]
Allahverdiyev, Adil M. [2 ]
机构
[1] Firat Univ, Dept Bioengn, TR-23169 Elazig, Turkey
[2] Yildiz Tekn Univ, Dept Bioengn, Istanbul, Turkey
关键词
Leishmaniasis; Polyacrylic acid; Synthetic polyelectrolytes; Infection; Antiparasitic agents; IN-VITRO; IMMUNOSTIMULATING PROPERTIES; HOST-CELL; INFECTIVITY; DONOVANI; PROMASTIGOTES; INHIBITION; POLYANIONS; SYNTHASE; VACCINE;
D O I
10.1016/j.exppara.2012.11.014
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
Polyacrylic acid (PAA) is one of the anionic synthetic polyelectrolytes and is used in various immunological and pharmaceutical applications. PAA has been used as adjuvant in veterinary vaccines, in particular. However, to our knowledge, there are no studies that document immunostimulant properties of PAA in Leishmania infection. The main aim of this study was to investigate the interaction of Leishmania parasites with PAA: the possible effects on the infectivity of Leishmania promastigotes; and, induction of nitric oxide (NO) production in macrophages in vitro. The cytotoxicity of PAA on both macrophages and Leishmania infantum promastigotes were determined by MTT assay. NO production in the macrophage culture supernatant was measured by the Griess method. A significant, dose-dependent and time-dependent decrease in the infection index was observed after PAA exposure. The value of this decrease was found to be between 93% and 100% for all concentration and time points. PAA (molecular weight (MW) 30, 100 kDa at 1 mg/1 h)-exposed parasites stimulate NO production significantly at 48 h post-infection (PI), when compared to the control. This study demonstrates that Leishmania parasites lost their virulence upon interaction with PAA, and this interaction induced NO production in infected macrophages. These results may have important implications in the development of anti-leishmanial vaccines and amelioration of immune response. (c) 2012 Elsevier Inc. All rights reserved.
引用
收藏
页码:237 / 242
页数:6
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