Pulmonary inflammation promoted by type-2 dendritic cells is a feature of human and murine schistosomiasis
E. L. Houlder,
A. H. Costain,
I. Nambuya,
S. L. Brown,
J. P. R. Koopman,
M. C. C. Langenberg,
J. J. Janse,
M. A. Hoogerwerf,
A. J. L. Ridley,
J. E. Forde-Thomas,
S. A. P. Colombo,
B. M. F. Winkel,
A. A. Galdon,
K. F. Hoffmann,
P. C. Cook,
M. Roestenberg,
H. Mpairwe and
A. S. MacDonald ()
Additional contact information
E. L. Houlder: University of Manchester
A. H. Costain: University of Manchester
I. Nambuya: University of Manchester
S. L. Brown: University of Manchester
J. P. R. Koopman: Leiden University Medical Centre
M. C. C. Langenberg: Leiden University Medical Centre
J. J. Janse: Leiden University Medical Centre
M. A. Hoogerwerf: Leiden University Medical Centre
A. J. L. Ridley: University of Manchester
J. E. Forde-Thomas: Aberystwyth University
S. A. P. Colombo: University of Manchester
B. M. F. Winkel: Leiden University Medical Centre
A. A. Galdon: University of Manchester
K. F. Hoffmann: Aberystwyth University
P. C. Cook: University of Manchester
M. Roestenberg: Leiden University Medical Centre
H. Mpairwe: MRC/UVRI and LSHTM Uganda Research Unit
A. S. MacDonald: University of Manchester
Nature Communications, 2023, vol. 14, issue 1, 1-12
Abstract:
Abstract Schistosomiasis is a parasitic disease affecting over 200 million people in multiple organs, including the lungs. Despite this, there is little understanding of pulmonary immune responses during schistosomiasis. Here, we show type-2 dominated lung immune responses in both patent (egg producing) and pre-patent (larval lung migration) murine Schistosoma mansoni (S. mansoni) infection. Human pre-patent S. mansoni infection pulmonary (sputum) samples revealed a mixed type-1/type-2 inflammatory cytokine profile, whilst a case-control study showed no significant pulmonary cytokine changes in endemic patent infection. However, schistosomiasis induced expansion of pulmonary type-2 conventional dendritic cells (cDC2s) in human and murine hosts, at both infection stages. Further, cDC2s were required for type-2 pulmonary inflammation in murine pre-patent or patent infection. These data elevate our fundamental understanding of pulmonary immune responses during schistosomiasis, which may be important for future vaccine design, as well as for understanding links between schistosomiasis and other lung diseases.
Date: 2023
References: View references in EconPapers View complete reference list from CitEc
Citations:
Downloads: (external link)
https://www.nature.com/articles/s41467-023-37502-z Abstract (text/html)
Related works:
This item may be available elsewhere in EconPapers: Search for items with the same title.
Export reference: BibTeX
RIS (EndNote, ProCite, RefMan)
HTML/Text
Persistent link: https://EconPapers.repec.org/RePEc:nat:natcom:v:14:y:2023:i:1:d:10.1038_s41467-023-37502-z
Ordering information: This journal article can be ordered from
https://www.nature.com/ncomms/
DOI: 10.1038/s41467-023-37502-z
Access Statistics for this article
Nature Communications is currently edited by Nathalie Le Bot, Enda Bergin and Fiona Gillespie
More articles in Nature Communications from Nature
Bibliographic data for series maintained by Sonal Shukla () and Springer Nature Abstracting and Indexing ().