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S. mansoni Trapping in Lungs Contributes to Resistance to Reinfection
Worm transplantation studies show that physiological and reproductive status of the worm is influenced by the microenvironment of the host and critical for vaccine design. Worm migration studies in rats with (75)Se-methionine labeled cercariae demonstrated that resistance to reinfection (R/R) requir...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4404922/ https://www.ncbi.nlm.nih.gov/pubmed/25954278 http://dx.doi.org/10.3389/fimmu.2015.00186 |
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author | Knopf, Paul Mark Suri, Parmjeet Behl |
author_facet | Knopf, Paul Mark Suri, Parmjeet Behl |
author_sort | Knopf, Paul Mark |
collection | PubMed |
description | Worm transplantation studies show that physiological and reproductive status of the worm is influenced by the microenvironment of the host and critical for vaccine design. Worm migration studies in rats with (75)Se-methionine labeled cercariae demonstrated that resistance to reinfection (R/R) requires a host immune response resulting in worm death. In permissive hosts, inflammation due to anti eggs immunity leads to host death, whereas in non-permissive hosts this is not the case due to reduced egg burdens. Eggs-induced pathology and inflammatory debris resulting from immune attack on worms are important for vaccine design. Protective immune responses are perhaps induced when naïve hosts are vaccinated with either schistosome-derived molecules or attenuated cercariae as suggested by the induction of protective anti-parasite antibodies and monoclonals. However, these immunological strategies rarely produce 85–90% R/R as is achievable by portal-caval shunting. Alternatively, induction of anti-schistosoma immunity may induce portacaval shunting, seems highly unlikely although not yet tested. Differential screening with sera from twice-infected rats, protective (F2x) from Fisher vs. non-protective (W2x) from Wistar–Furth rats, was used to identify candidate vaccine antigens. |
format | Online Article Text |
id | pubmed-4404922 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-44049222015-05-07 S. mansoni Trapping in Lungs Contributes to Resistance to Reinfection Knopf, Paul Mark Suri, Parmjeet Behl Front Immunol Immunology Worm transplantation studies show that physiological and reproductive status of the worm is influenced by the microenvironment of the host and critical for vaccine design. Worm migration studies in rats with (75)Se-methionine labeled cercariae demonstrated that resistance to reinfection (R/R) requires a host immune response resulting in worm death. In permissive hosts, inflammation due to anti eggs immunity leads to host death, whereas in non-permissive hosts this is not the case due to reduced egg burdens. Eggs-induced pathology and inflammatory debris resulting from immune attack on worms are important for vaccine design. Protective immune responses are perhaps induced when naïve hosts are vaccinated with either schistosome-derived molecules or attenuated cercariae as suggested by the induction of protective anti-parasite antibodies and monoclonals. However, these immunological strategies rarely produce 85–90% R/R as is achievable by portal-caval shunting. Alternatively, induction of anti-schistosoma immunity may induce portacaval shunting, seems highly unlikely although not yet tested. Differential screening with sera from twice-infected rats, protective (F2x) from Fisher vs. non-protective (W2x) from Wistar–Furth rats, was used to identify candidate vaccine antigens. Frontiers Media S.A. 2015-04-21 /pmc/articles/PMC4404922/ /pubmed/25954278 http://dx.doi.org/10.3389/fimmu.2015.00186 Text en Copyright © 2015 Knopf and Suri. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Immunology Knopf, Paul Mark Suri, Parmjeet Behl S. mansoni Trapping in Lungs Contributes to Resistance to Reinfection |
title | S. mansoni Trapping in Lungs Contributes to Resistance to Reinfection |
title_full | S. mansoni Trapping in Lungs Contributes to Resistance to Reinfection |
title_fullStr | S. mansoni Trapping in Lungs Contributes to Resistance to Reinfection |
title_full_unstemmed | S. mansoni Trapping in Lungs Contributes to Resistance to Reinfection |
title_short | S. mansoni Trapping in Lungs Contributes to Resistance to Reinfection |
title_sort | s. mansoni trapping in lungs contributes to resistance to reinfection |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4404922/ https://www.ncbi.nlm.nih.gov/pubmed/25954278 http://dx.doi.org/10.3389/fimmu.2015.00186 |
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