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Surfactant Protein-D Is Essential for Immunity to Helminth Infection
Pulmonary epithelial cell responses can enhance type 2 immunity and contribute to control of nematode infections. An important epithelial product is the collectin Surfactant Protein D (SP-D). We found that SP-D concentrations increased in the lung following Nippostrongylus brasiliensis infection; th...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4763345/ https://www.ncbi.nlm.nih.gov/pubmed/26900854 http://dx.doi.org/10.1371/journal.ppat.1005461 |
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author | Thawer, Sumaiyya Auret, Jennifer Schnoeller, Corinna Chetty, Alisha Smith, Katherine Darby, Matthew Roberts, Luke Mackay, Rosie-Marie Whitwell, Harry J. Timms, John F. Madsen, Jens Selkirk, Murray E. Brombacher, Frank Clark, Howard William Horsnell, William G. C. |
author_facet | Thawer, Sumaiyya Auret, Jennifer Schnoeller, Corinna Chetty, Alisha Smith, Katherine Darby, Matthew Roberts, Luke Mackay, Rosie-Marie Whitwell, Harry J. Timms, John F. Madsen, Jens Selkirk, Murray E. Brombacher, Frank Clark, Howard William Horsnell, William G. C. |
author_sort | Thawer, Sumaiyya |
collection | PubMed |
description | Pulmonary epithelial cell responses can enhance type 2 immunity and contribute to control of nematode infections. An important epithelial product is the collectin Surfactant Protein D (SP-D). We found that SP-D concentrations increased in the lung following Nippostrongylus brasiliensis infection; this increase was dependent on key components of the type 2 immune response. We carried out loss and gain of function studies of SP-D to establish if SP-D was required for optimal immunity to the parasite. N. brasiliensis infection of SP-D-/- mice resulted in profound impairment of host innate immunity and ability to resolve infection. Raising pulmonary SP-D levels prior to infection enhanced parasite expulsion and type 2 immune responses, including increased numbers of IL-13 producing type 2 innate lymphoid cells (ILC2), elevated expression of markers of alternative activation by alveolar macrophages (alvM) and increased production of the type 2 cytokines IL-4 and IL-13. Adoptive transfer of alvM from SP-D-treated parasite infected mice into naïve recipients enhanced immunity to N. brasiliensis. Protection was associated with selective binding by the SP-D carbohydrate recognition domain (CRD) to L4 parasites to enhance their killing by alvM. These findings are the first demonstration that the collectin SP-D is an essential component of host innate immunity to helminths. |
format | Online Article Text |
id | pubmed-4763345 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-47633452016-03-07 Surfactant Protein-D Is Essential for Immunity to Helminth Infection Thawer, Sumaiyya Auret, Jennifer Schnoeller, Corinna Chetty, Alisha Smith, Katherine Darby, Matthew Roberts, Luke Mackay, Rosie-Marie Whitwell, Harry J. Timms, John F. Madsen, Jens Selkirk, Murray E. Brombacher, Frank Clark, Howard William Horsnell, William G. C. PLoS Pathog Research Article Pulmonary epithelial cell responses can enhance type 2 immunity and contribute to control of nematode infections. An important epithelial product is the collectin Surfactant Protein D (SP-D). We found that SP-D concentrations increased in the lung following Nippostrongylus brasiliensis infection; this increase was dependent on key components of the type 2 immune response. We carried out loss and gain of function studies of SP-D to establish if SP-D was required for optimal immunity to the parasite. N. brasiliensis infection of SP-D-/- mice resulted in profound impairment of host innate immunity and ability to resolve infection. Raising pulmonary SP-D levels prior to infection enhanced parasite expulsion and type 2 immune responses, including increased numbers of IL-13 producing type 2 innate lymphoid cells (ILC2), elevated expression of markers of alternative activation by alveolar macrophages (alvM) and increased production of the type 2 cytokines IL-4 and IL-13. Adoptive transfer of alvM from SP-D-treated parasite infected mice into naïve recipients enhanced immunity to N. brasiliensis. Protection was associated with selective binding by the SP-D carbohydrate recognition domain (CRD) to L4 parasites to enhance their killing by alvM. These findings are the first demonstration that the collectin SP-D is an essential component of host innate immunity to helminths. Public Library of Science 2016-02-22 /pmc/articles/PMC4763345/ /pubmed/26900854 http://dx.doi.org/10.1371/journal.ppat.1005461 Text en © 2016 Thawer 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 Thawer, Sumaiyya Auret, Jennifer Schnoeller, Corinna Chetty, Alisha Smith, Katherine Darby, Matthew Roberts, Luke Mackay, Rosie-Marie Whitwell, Harry J. Timms, John F. Madsen, Jens Selkirk, Murray E. Brombacher, Frank Clark, Howard William Horsnell, William G. C. Surfactant Protein-D Is Essential for Immunity to Helminth Infection |
title | Surfactant Protein-D Is Essential for Immunity to Helminth Infection |
title_full | Surfactant Protein-D Is Essential for Immunity to Helminth Infection |
title_fullStr | Surfactant Protein-D Is Essential for Immunity to Helminth Infection |
title_full_unstemmed | Surfactant Protein-D Is Essential for Immunity to Helminth Infection |
title_short | Surfactant Protein-D Is Essential for Immunity to Helminth Infection |
title_sort | surfactant protein-d is essential for immunity to helminth infection |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4763345/ https://www.ncbi.nlm.nih.gov/pubmed/26900854 http://dx.doi.org/10.1371/journal.ppat.1005461 |
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