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Prof. Mona Elsayed Nasr Sakr :: Publications:

Title:
Lung-Phase resistance against challenged Schistosoma mansoni infection in mice immunized with soluble egg antigen.
Authors: Magda M. Sanad, Raefa A. Darwish, Yousef S. M., Mona E. Nasr and Mahmoud W. Emara
Year: 1996
Keywords: Not Available
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Local/International: Local
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Abstract:

A histological and immunohistochemical study was made on Schistosomula, associated inflammatory reaction and of Schistosomal antigens in lung tissues of normal mice and mice immunized with partially purified soluble egg antigen (SEA) of molecular weight 100-137 k daltons. Schistosomula and inflammatory foci were counted by histologic scoring in 20 lung section/mouse taken at intervals of 30μ apart. Results Showed that in normal mice, Schistosomula number reached their peak on day 7 post infection then rapidly decreased until they were barely detectable on day 25. In immunized mice, they reached their peak on day 9 than gradually decreased so as many worms were still retained in the lungs on day 25. That is, the rate of elimination of lung Schistosomula was much slower in immunized mice. The pulmonary cellular reaction in immunized mice was evident as early as day 7 and from day 9 onwords, mononuclear infiltrations were increasing. Inflammatory foci appeared earlier (day 7) and significantly increased on subsequent days. The reaction, therefore, was anamnestic, most probably of delayed type hypersensitivity (DTH) response. In normal mice, the reaction was mild and started late. Schistosomal antigen deposition in lung tissues was markedly augmented in immunized mice with more consequent stimulation of the immune response. So, this study indicates that immunization with this type of antigen causes augmentative lung resistance against challenge infection as it was effective in blocking migration of schistosomula by stimulating inflammation in lung tissues and so may be of value in vaccination studies against schistosomiasis. However, it should be necessary to guard against excessive inflammation and pulmonary fibrosis.

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