Please use this identifier to cite or link to this item: http://nopr.niscair.res.in/handle/123456789/6538
Title: Excretory-secretory product of <i style="">Fasciola hepatica</i> worm protects against <i style="">Schistosoma mansoni</i> infection in mice
Authors: Hamed, Manal A
Keywords: Antioxidant
Enzymes
Excrtory- secretory antigen
<i style="">Fasciola hepatica</i>
<i style="">Schistosoma mansoni</i>
Issue Date: Jul-2006
Publisher: CSIR
Abstract: The objective of this study was to evaluate the protective immunity of excretory-secretory products of <i style="">Fasciola hepatica </i>(FhES) worm against <i style="">S.mansoni</i> infection in mice. Evaluation of FhES antigen was through measuring worm burden, ova count, granuloma size and frequency as well as the histopathological picture of the liver. The study was extended to determine the level of free radical scavengers; lipid peroxide, glutathione (GSH), vitamin C, vitamin E, catalase and superoxide dismutase (SOD). Liver function enzymes such as aspartate aminotransferase (AST), alanine aminotransferase (ALT) and alkaline phosphatase (ALP) were also taken into consideration. Four groups of eight mice each were selected for this study. Group 1 served as control group. Group 2: normal healthy mice vaccinated with FhES product. Group 3: <i style="">S.mansoni</i> infected mice for 2 months and group 4: infected mice pre-vaccinated with FhES antigen. Vaccination schedule comprised of a single subcutaneous injection of FhES antigen emulsified with Freund’s complete adjuvant in a dose 0.5 mg protein/mouse, followed by intraperitoneal injections of the same antigen without adjuvant in 3 doses/week for 3 successive weeks. The total antigen inoculation was 5 mg protein/mouse. The present results revealed a drastic change in all the measured parameters after <i style="">S.mansoni</i> infection and a noticeable improved level after vaccination with FhES antigen. It can be concluded that FhES antigen succeeded to protect mice against schistosomiasis by a significant reduction in worm burden, ova count, granuloma size and number, improvement in the histopathological architecture of the liver as well as amelioration in the antioxidant levels under investigation.
Description: 554-561
URI: http://hdl.handle.net/123456789/6538
ISSN: 0975-1009 (Online); 0019-5189 (Print)
Appears in Collections:IJEB Vol.44(07) [July 2006]

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