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Helminth parasites and immune regulation

Helminth parasites are complex metazoans that belong to different taxonomic families but that collectively share the capacity to downregulate the host immune response directed toward themselves (parasite-specific immunoregulation). During long-standing chronic infection, these helminths appear able...

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Autores principales: Gazzinelli-Guimaraes, Pedro H., Nutman, Thomas B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: F1000 Research Limited 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6206608/
https://www.ncbi.nlm.nih.gov/pubmed/30416709
http://dx.doi.org/10.12688/f1000research.15596.1
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author Gazzinelli-Guimaraes, Pedro H.
Nutman, Thomas B.
author_facet Gazzinelli-Guimaraes, Pedro H.
Nutman, Thomas B.
author_sort Gazzinelli-Guimaraes, Pedro H.
collection PubMed
description Helminth parasites are complex metazoans that belong to different taxonomic families but that collectively share the capacity to downregulate the host immune response directed toward themselves (parasite-specific immunoregulation). During long-standing chronic infection, these helminths appear able to suppress immune responses to bystander pathogens/antigens and atopic, autoimmune, and metabolic disorders. Helminth-induced immunoregulation occurs through the induction of regulatory T cells or Th2-type cells (or both). However, secreted or excreted parasite metabolites, proteins, or extracellular vesicles (or a combination of these) may also directly induce signaling pathways in host cells. Therefore, the focus of this review will be to highlight recent advances in understanding the immune responses to helminth infection, emphasizing the strategies/molecules and some of the mechanisms used by helminth parasites to modulate the immune response of their hosts.
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spelling pubmed-62066082018-11-09 Helminth parasites and immune regulation Gazzinelli-Guimaraes, Pedro H. Nutman, Thomas B. F1000Res Review Helminth parasites are complex metazoans that belong to different taxonomic families but that collectively share the capacity to downregulate the host immune response directed toward themselves (parasite-specific immunoregulation). During long-standing chronic infection, these helminths appear able to suppress immune responses to bystander pathogens/antigens and atopic, autoimmune, and metabolic disorders. Helminth-induced immunoregulation occurs through the induction of regulatory T cells or Th2-type cells (or both). However, secreted or excreted parasite metabolites, proteins, or extracellular vesicles (or a combination of these) may also directly induce signaling pathways in host cells. Therefore, the focus of this review will be to highlight recent advances in understanding the immune responses to helminth infection, emphasizing the strategies/molecules and some of the mechanisms used by helminth parasites to modulate the immune response of their hosts. F1000 Research Limited 2018-10-23 /pmc/articles/PMC6206608/ /pubmed/30416709 http://dx.doi.org/10.12688/f1000research.15596.1 Text en Copyright: © 2018 Gazzinelli-Guimaraes PH and Nutman TB http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The author(s) is/are employees of the US Government and therefore domestic copyright protection in USA does not apply to this work. The work may be protected under the copyright laws of other jurisdictions when used in those jurisdictions.
spellingShingle Review
Gazzinelli-Guimaraes, Pedro H.
Nutman, Thomas B.
Helminth parasites and immune regulation
title Helminth parasites and immune regulation
title_full Helminth parasites and immune regulation
title_fullStr Helminth parasites and immune regulation
title_full_unstemmed Helminth parasites and immune regulation
title_short Helminth parasites and immune regulation
title_sort helminth parasites and immune regulation
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6206608/
https://www.ncbi.nlm.nih.gov/pubmed/30416709
http://dx.doi.org/10.12688/f1000research.15596.1
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