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Schistosome Infection Intensity Is Inversely Related to Auto-Reactive Antibody Levels

In animal experimental models, parasitic helminth infections can protect the host from auto-immune diseases. We conducted a population-scale human study investigating the relationship between helminth parasitism and auto-reactive antibodies and the subsequent effect of anti-helminthic treatment on t...

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Autores principales: Mutapi, Francisca, Imai, Natsuko, Nausch, Norman, Bourke, Claire D., Rujeni, Nadine, Mitchell, Kate M., Midzi, Nicholas, Woolhouse, Mark E. J., Maizels, Rick M., Mduluza, Takafira
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3089602/
https://www.ncbi.nlm.nih.gov/pubmed/21573157
http://dx.doi.org/10.1371/journal.pone.0019149
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author Mutapi, Francisca
Imai, Natsuko
Nausch, Norman
Bourke, Claire D.
Rujeni, Nadine
Mitchell, Kate M.
Midzi, Nicholas
Woolhouse, Mark E. J.
Maizels, Rick M.
Mduluza, Takafira
author_facet Mutapi, Francisca
Imai, Natsuko
Nausch, Norman
Bourke, Claire D.
Rujeni, Nadine
Mitchell, Kate M.
Midzi, Nicholas
Woolhouse, Mark E. J.
Maizels, Rick M.
Mduluza, Takafira
author_sort Mutapi, Francisca
collection PubMed
description In animal experimental models, parasitic helminth infections can protect the host from auto-immune diseases. We conducted a population-scale human study investigating the relationship between helminth parasitism and auto-reactive antibodies and the subsequent effect of anti-helminthic treatment on this relationship. Levels of antinuclear antibodies (ANA) and plasma IL-10 were measured by enzyme linked immunosorbent assay in 613 Zimbabweans (aged 2–86 years) naturally exposed to the blood fluke Schistosoma haematobium. ANA levels were related to schistosome infection intensity and systemic IL-10 levels. All participants were offered treatment with the anti-helminthic drug praziquantel and 102 treated schoolchildren (5–16 years) were followed up 6 months post-antihelminthic treatment. ANA levels were inversely associated with current infection intensity but were independent of host age, sex and HIV status. Furthermore, after allowing for the confounding effects of schistosome infection intensity, ANA levels were inversely associated with systemic levels of IL-10. ANA levels increased significantly 6 months after anti-helminthic treatment. Our study shows that ANA levels are attenuated in helminth-infected humans and that anti-helminthic treatment of helminth-infected people can significantly increase ANA levels. The implications of these findings are relevant for understanding both the aetiology of immune disorders mediated by auto-reactive antibodies and in predicting the long-term consequences of large-scale schistosomiasis control programs.
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spelling pubmed-30896022011-05-13 Schistosome Infection Intensity Is Inversely Related to Auto-Reactive Antibody Levels Mutapi, Francisca Imai, Natsuko Nausch, Norman Bourke, Claire D. Rujeni, Nadine Mitchell, Kate M. Midzi, Nicholas Woolhouse, Mark E. J. Maizels, Rick M. Mduluza, Takafira PLoS One Research Article In animal experimental models, parasitic helminth infections can protect the host from auto-immune diseases. We conducted a population-scale human study investigating the relationship between helminth parasitism and auto-reactive antibodies and the subsequent effect of anti-helminthic treatment on this relationship. Levels of antinuclear antibodies (ANA) and plasma IL-10 were measured by enzyme linked immunosorbent assay in 613 Zimbabweans (aged 2–86 years) naturally exposed to the blood fluke Schistosoma haematobium. ANA levels were related to schistosome infection intensity and systemic IL-10 levels. All participants were offered treatment with the anti-helminthic drug praziquantel and 102 treated schoolchildren (5–16 years) were followed up 6 months post-antihelminthic treatment. ANA levels were inversely associated with current infection intensity but were independent of host age, sex and HIV status. Furthermore, after allowing for the confounding effects of schistosome infection intensity, ANA levels were inversely associated with systemic levels of IL-10. ANA levels increased significantly 6 months after anti-helminthic treatment. Our study shows that ANA levels are attenuated in helminth-infected humans and that anti-helminthic treatment of helminth-infected people can significantly increase ANA levels. The implications of these findings are relevant for understanding both the aetiology of immune disorders mediated by auto-reactive antibodies and in predicting the long-term consequences of large-scale schistosomiasis control programs. Public Library of Science 2011-05-06 /pmc/articles/PMC3089602/ /pubmed/21573157 http://dx.doi.org/10.1371/journal.pone.0019149 Text en Mutapi et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Mutapi, Francisca
Imai, Natsuko
Nausch, Norman
Bourke, Claire D.
Rujeni, Nadine
Mitchell, Kate M.
Midzi, Nicholas
Woolhouse, Mark E. J.
Maizels, Rick M.
Mduluza, Takafira
Schistosome Infection Intensity Is Inversely Related to Auto-Reactive Antibody Levels
title Schistosome Infection Intensity Is Inversely Related to Auto-Reactive Antibody Levels
title_full Schistosome Infection Intensity Is Inversely Related to Auto-Reactive Antibody Levels
title_fullStr Schistosome Infection Intensity Is Inversely Related to Auto-Reactive Antibody Levels
title_full_unstemmed Schistosome Infection Intensity Is Inversely Related to Auto-Reactive Antibody Levels
title_short Schistosome Infection Intensity Is Inversely Related to Auto-Reactive Antibody Levels
title_sort schistosome infection intensity is inversely related to auto-reactive antibody levels
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3089602/
https://www.ncbi.nlm.nih.gov/pubmed/21573157
http://dx.doi.org/10.1371/journal.pone.0019149
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