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Surfactant Protein-D is essential for immunity to helminth infection

Surfactant Protein-D is essential for immunity to helminth infection
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; 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.
1553-7366
Thawer, Sumaiyya
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Auret, Jennifer
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Schnoeller, Corinna
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Chetty, Alisha
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Smith, Katherine
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Darby, Matthew
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Roberts, Luke
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Mackay, Rosie-Marie
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Whitwell, Harry J.
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Timms, John F.
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Madsen, Jens
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Selkirk, Murray E.
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Brombacher, Frank
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Clark, Howard William
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Horsnell, William G.C.
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Thawer, Sumaiyya
c595802c-3ced-4578-a07e-9453233a6ba6
Auret, Jennifer
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Schnoeller, Corinna
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Chetty, Alisha
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Smith, Katherine
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Darby, Matthew
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Roberts, Luke
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Mackay, Rosie-Marie
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Whitwell, Harry J.
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Timms, John F.
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Madsen, Jens
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Selkirk, Murray E.
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Brombacher, Frank
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Clark, Howard William
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Horsnell, William G.C.
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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 and Horsnell, William G.C. (2016) Surfactant Protein-D is essential for immunity to helminth infection. PLOS Pathogens, 12 (2), [e1005461]. (doi:10.1371/journal.ppat.1005461). (PMID:26900854)

Record type: Article

Abstract

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.

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Accepted/In Press date: 28 January 2016
e-pub ahead of print date: 22 February 2016
Published date: 22 February 2016
Organisations: Clinical & Experimental Sciences

Identifiers

Local EPrints ID: 395458
URI: http://eprints.soton.ac.uk/id/eprint/395458
ISSN: 1553-7366
PURE UUID: 96f8317f-d95f-4b9b-8175-40b7c8de42e6
ORCID for Rosie-Marie Mackay: ORCID iD orcid.org/0000-0002-9493-9654
ORCID for Jens Madsen: ORCID iD orcid.org/0000-0003-1664-7645

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Date deposited: 31 May 2016 10:06
Last modified: 15 Mar 2024 03:29

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Contributors

Author: Sumaiyya Thawer
Author: Jennifer Auret
Author: Corinna Schnoeller
Author: Alisha Chetty
Author: Katherine Smith
Author: Matthew Darby
Author: Luke Roberts
Author: Rosie-Marie Mackay ORCID iD
Author: Harry J. Whitwell
Author: John F. Timms
Author: Jens Madsen ORCID iD
Author: Murray E. Selkirk
Author: Frank Brombacher
Author: Howard William Clark
Author: William G.C. Horsnell

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