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.
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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22 February 2016
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, 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)
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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THAWER - PLoS Pathogens - SPD is essential for immunity in helminth infection.pdf
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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
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Local EPrints ID: 395458
URI: http://eprints.soton.ac.uk/id/eprint/395458
ISSN: 1553-7366
PURE UUID: 96f8317f-d95f-4b9b-8175-40b7c8de42e6
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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
Author:
Harry J. Whitwell
Author:
John F. Timms
Author:
Jens Madsen
Author:
Murray E. Selkirk
Author:
Frank Brombacher
Author:
Howard William Clark
Author:
William G.C. Horsnell
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