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Immunopathological Changes in the Brain of Immunosuppressed Mice Experimentally Infected with Toxocara canis
Toxocariasis is a soil-transmitted helminthozoonosis due to infection of humans by larvae of Toxocara canis. The disease could produce cognitive and behavioral disturbances especially in children. Meanwhile, in our modern era, the incidence of immunosuppression has been progressively increasing due...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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The Korean Society for Parasitology and Tropical Medicine
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4384791/ https://www.ncbi.nlm.nih.gov/pubmed/25748709 http://dx.doi.org/10.3347/kjp.2015.53.1.51 |
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author | Eid, Mohamed M. El-Kowrany, Samy I. Othman, Ahmad A. Gendy, Dina I. El Saied, Eman M. |
author_facet | Eid, Mohamed M. El-Kowrany, Samy I. Othman, Ahmad A. Gendy, Dina I. El Saied, Eman M. |
author_sort | Eid, Mohamed M. |
collection | PubMed |
description | Toxocariasis is a soil-transmitted helminthozoonosis due to infection of humans by larvae of Toxocara canis. The disease could produce cognitive and behavioral disturbances especially in children. Meanwhile, in our modern era, the incidence of immunosuppression has been progressively increasing due to increased incidence of malignancy as well as increased use of immunosuppressive agents. The present study aimed at comparing some of the pathological and immunological alterations in the brain of normal and immunosuppressed mice experimentally infected with T. canis. Therefore, 180 Swiss albino mice were divided into 4 groups including normal (control) group, immunocompetent T. canis-infected group, immunosuppressed group (control), and immunosuppressed infected group. Infected mice were subjected to larval counts in the brain, and the brains from all mice were assessed for histopathological changes, astrogliosis, and IL-5 mRNA expression levels in brain tissues. The results showed that under immunosuppression, there were significant increase in brain larval counts, significant enhancement of reactive gliosis, and significant reduction in IL-5 mRNA expression. All these changes were maximal in the chronic stage of infection. In conclusion, the immunopathological alterations in the brains of infected animals were progressive over time, and were exaggerated under the effect of immunosuppression as did the intensity of cerebral infection. |
format | Online Article Text |
id | pubmed-4384791 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | The Korean Society for Parasitology and Tropical Medicine |
record_format | MEDLINE/PubMed |
spelling | pubmed-43847912015-04-09 Immunopathological Changes in the Brain of Immunosuppressed Mice Experimentally Infected with Toxocara canis Eid, Mohamed M. El-Kowrany, Samy I. Othman, Ahmad A. Gendy, Dina I. El Saied, Eman M. Korean J Parasitol Original Article Toxocariasis is a soil-transmitted helminthozoonosis due to infection of humans by larvae of Toxocara canis. The disease could produce cognitive and behavioral disturbances especially in children. Meanwhile, in our modern era, the incidence of immunosuppression has been progressively increasing due to increased incidence of malignancy as well as increased use of immunosuppressive agents. The present study aimed at comparing some of the pathological and immunological alterations in the brain of normal and immunosuppressed mice experimentally infected with T. canis. Therefore, 180 Swiss albino mice were divided into 4 groups including normal (control) group, immunocompetent T. canis-infected group, immunosuppressed group (control), and immunosuppressed infected group. Infected mice were subjected to larval counts in the brain, and the brains from all mice were assessed for histopathological changes, astrogliosis, and IL-5 mRNA expression levels in brain tissues. The results showed that under immunosuppression, there were significant increase in brain larval counts, significant enhancement of reactive gliosis, and significant reduction in IL-5 mRNA expression. All these changes were maximal in the chronic stage of infection. In conclusion, the immunopathological alterations in the brains of infected animals were progressive over time, and were exaggerated under the effect of immunosuppression as did the intensity of cerebral infection. The Korean Society for Parasitology and Tropical Medicine 2015-02 2015-02-27 /pmc/articles/PMC4384791/ /pubmed/25748709 http://dx.doi.org/10.3347/kjp.2015.53.1.51 Text en © 2015, Korean Society for Parasitology and Tropical Medicine This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Eid, Mohamed M. El-Kowrany, Samy I. Othman, Ahmad A. Gendy, Dina I. El Saied, Eman M. Immunopathological Changes in the Brain of Immunosuppressed Mice Experimentally Infected with Toxocara canis |
title | Immunopathological Changes in the Brain of Immunosuppressed Mice Experimentally Infected with Toxocara canis |
title_full | Immunopathological Changes in the Brain of Immunosuppressed Mice Experimentally Infected with Toxocara canis |
title_fullStr | Immunopathological Changes in the Brain of Immunosuppressed Mice Experimentally Infected with Toxocara canis |
title_full_unstemmed | Immunopathological Changes in the Brain of Immunosuppressed Mice Experimentally Infected with Toxocara canis |
title_short | Immunopathological Changes in the Brain of Immunosuppressed Mice Experimentally Infected with Toxocara canis |
title_sort | immunopathological changes in the brain of immunosuppressed mice experimentally infected with toxocara canis |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4384791/ https://www.ncbi.nlm.nih.gov/pubmed/25748709 http://dx.doi.org/10.3347/kjp.2015.53.1.51 |
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