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      A helminth-derived suppressor of ST2 blocks allergic responses

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          Abstract

          The IL-33-ST2 pathway is an important initiator of type 2 immune responses. We previously characterised the HpARI protein secreted by the model intestinal nematode Heligmosomoides polygyrus, which binds and blocks IL-33. Here, we identify H. polygyrus Binds Alarmin Receptor and Inhibits (HpBARI) and HpBARI_Hom2, both of which consist of complement control protein (CCP) domains, similarly to the immunomodulatory HpARI and Hp-TGM proteins. HpBARI binds murine ST2, inhibiting cell surface detection of ST2, preventing IL-33-ST2 interactions, and inhibiting IL-33 responses in vitro and in an in vivo mouse model of asthma. In H. polygyrus infection, ST2 detection is abrogated in the peritoneal cavity and lung, consistent with systemic effects of HpBARI. HpBARI_Hom2 also binds human ST2 with high affinity, and effectively blocks human PBMC responses to IL-33. Thus, we show that H. polygyrus blocks the IL-33 pathway via both HpARI which blocks the cytokine, and also HpBARI which blocks the receptor.

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          WormBase ParaSite − a comprehensive resource for helminth genomics

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            Tissue signals imprint ILC2 identity with anticipatory function

            Group 2 innate lymphoid cells (ILC2s) are distributed systemically and produce type 2 cytokines in response to a variety of stimuli, including the epithelial cytokines interleukin (IL)-25, IL-33, and thymic stromal lymphopoietin (TSLP). Transcriptional profiling of ILC2s from different tissues, however, grouped ILC2s according to their tissue of origin, even in the setting of combined IL-25, IL-33R and TSLPR-deficiency. Single-cell profiling confirmed a tissue-organizing transcriptome and identified ILC2 subsets expressing distinct activating receptors, including the major subset of skin ILC2s, which were activated preferentially by IL-18. Tissue ILC2 subsets were unaltered in number and expression in germ-free mice, suggesting that endogenous, tissue-derived signals drive the maturation of ILC2 subsets by controlling expression of distinct patterns of activating receptors, thus anticipating tissue-specific perturbations occurring later in life.
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              A genome-wide association study identifies CDHR3 as a susceptibility locus for early childhood asthma with severe exacerbations.

              Asthma exacerbations are among the most frequent causes of hospitalization during childhood, but the underlying mechanisms are poorly understood. We performed a genome-wide association study of a specific asthma phenotype characterized by recurrent, severe exacerbations occurring between 2 and 6 years of age in a total of 1,173 cases and 2,522 controls. Cases were identified from national health registries of hospitalization, and DNA was obtained from the Danish Neonatal Screening Biobank. We identified five loci with genome-wide significant association. Four of these, GSDMB, IL33, RAD50 and IL1RL1, were previously reported as asthma susceptibility loci, but the effect sizes for these loci in our cohort were considerably larger than in the previous genome-wide association studies of asthma. We also obtained strong evidence for a new susceptibility gene, CDHR3 (encoding cadherin-related family member 3), which is highly expressed in airway epithelium. These results demonstrate the strength of applying specific phenotyping in the search for asthma susceptibility genes.
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                Author and article information

                Contributors
                Role: Senior Editor
                Role: Reviewing Editor
                Journal
                eLife
                Elife
                eLife
                eLife
                eLife Sciences Publications, Ltd
                2050-084X
                18 May 2020
                2020
                : 9
                : e54017
                Affiliations
                [1 ]Centre for Inflammation Research, University of Edinburgh, Queen’s Medical Research Institute EdinburghUnited Kingdom
                [2 ]Department of Biochemistry, University of Oxford OxfordUnited Kingdom
                [3 ]Bioscience Asthma, Research and Early Development, Respiratory & Immunology, BioPharmaceuticals R&D, AstraZeneca CambridgeUnited Kingdom
                [4 ]Institute of Infection, Immunity and Inflammation, University of Glasgow GlasgowUnited Kingdom
                [5 ]Division of Cell Signalling and Immunology, School of Life Sciences, Wellcome Trust Building, University of Dundee DundeeUnited Kingdom
                [6 ]Division of Microbiology & Parasitology, Department of Pathology, University of Cambridge, Tennis Court Road CambridgeUnited Kingdom
                [7 ]The Edinburgh Protein Production Facility (EPPF), Wellcome Trust Centre for Cell Biology (WTCCB), University of Edinburgh EdinburghUnited Kingdom
                Institute of Industrial Science, The University of Tokyo Japan
                University of Washington United States
                University of Washington United States
                Author information
                https://orcid.org/0000-0001-6808-5221
                http://orcid.org/0000-0002-2870-1955
                https://orcid.org/0000-0003-1300-7407
                Article
                54017
                10.7554/eLife.54017
                7234810
                32420871
                989019c0-fe44-491d-a8cf-42ed05beae7e
                © 2020, Vacca et al

                This article is distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use and redistribution provided that the original author and source are credited.

                History
                : 28 November 2019
                : 06 May 2020
                Funding
                Funded by: Longfonds | Accelerate;
                Award ID: The AWWA project
                Award Recipient :
                Funded by: FundRef http://dx.doi.org/10.13039/501100000265, Medical Research Council;
                Award ID: MR/S000593/1
                Award Recipient :
                The funders had no role in study design, data collection and interpretation, or the decision to submit the work for publication.
                Categories
                Research Article
                Immunology and Inflammation
                Microbiology and Infectious Disease
                Custom metadata
                HpBARI is a protein secreted by a parasitic helminth, which binds to and blocks the IL-33 receptor, suppressing IL-33-dependent type 2 immune responses.

                Life sciences
                allergy,asthma,helminth,parasite,il-33,st2,human,mouse
                Life sciences
                allergy, asthma, helminth, parasite, il-33, st2, human, mouse

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