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de los Reyes Jimenez, M. ; Lechner, A. ; Alessandrini, F. ; Bohnacker, S. ; Schindela, S. ; Trompette, A.* ; Haimerl, P. ; Thomas, D.* ; Henkel, F. ; Mourao, A. ; Geerlof, A. ; da Costa, C.P.* ; Chaker, A. ; Brüne, B.* ; Nüsing, R.* ; Jakobsson, P.J.* ; Nockher, W.A.* ; Feige, M.J.* ; Haslbeck, M.* ; Ohnmacht, C. ; Marsland, B.J.* ; Voehringer, D.* ; Harris, N.L.* ; Schmidt-Weber, C.B. ; Esser-von Bieren, J.

An anti-inflammatory eicosanoid switch mediates the suppression of type-2 inflammation by helminth larval products.

Sci. Transl. Med. 12:eaay0605 (2020)
Verlagsversion Postprint DOI PMC
Open Access Green
Eicosanoids are key mediators of type-2 inflammation, e.g., in allergy and asthma. Helminth products have been suggested as remedies against inflammatory diseases, but their effects on eicosanoids are unknown. Here, we show that larval products of the helminth Heligmosomoides polygyrus bakeri (HpbE), known to modulate type-2 responses, trigger a broad anti-inflammatory eicosanoid shift by suppressing the 5-lipoxygenase pathway, but inducing the cyclooxygenase (COX) pathway. In human macrophages and granulocytes, the HpbE-driven induction of the COX pathway resulted in the production of anti-inflammatory mediators [e.g., prostaglandin E-2 (PGE(2)) and IL-10] and suppressed chemotaxis. HpbE also abrogated the chemotaxis of granulocytes from patients suffering from aspirin-exacerbated respiratory disease (AERD), a severe type-2 inflammatory condition. Intranasal treatment with HpbE extract attenuated allergic airway inflammation in mice, and intranasal transfer of HpbE-conditioned macrophages led to reduced airway eosinophilia in a COX/PGE(2)-dependent fashion. The induction of regulatory mediators in macrophages depended on p38 mitogen-activated protein kinase (MAPK), hypoxia-inducible factor-1 alpha (HIF-1 alpha), and Hpb glutamate dehydrogenase (GDH), which we identify as a major immunoregulatory protein in HpbE. Hpb GDH activity was required for anti-inflammatory effects of HpbE in macrophages, and local administration of recombinant Hpb GDH to the airways abrogated allergic airway inflammation in mice. Thus, a metabolic enzyme present in helminth larvae can suppress type-2 inflammation by inducing an anti-inflammatory eicosanoid switch, which has important implications for the therapy of allergy and asthma.
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Publikationstyp Artikel: Journalartikel
Dokumenttyp Wissenschaftlicher Artikel
Schlagwörter Allergic Airway Inflammation; House-dust Mite; Lung Inflammation; Alveolar Macrophages; Immunity; Receptor; Accumulation; Leukotrienes; Homeostasis; Inhibition
Sprache englisch
Veröffentlichungsjahr 2020
HGF-Berichtsjahr 2020
ISSN (print) / ISBN 1946-6234
e-ISSN 1946-6242
Zeitschrift Science Translational Medicine
Quellenangaben Band: 12, Heft: 540, Seiten: , Artikelnummer: eaay0605 Supplement: ,
Verlag American Association for the Advancement of Science (AAAS)
Verlagsort 1200 New York Ave, Nw, Washington, Dc 20005 Usa
Begutachtungsstatus Peer reviewed
Institut(e) Institute for Allergy Research (IAF)
Institute of Structural Biology (STB)
POF Topic(s) 30202 - Environmental Health
30203 - Molecular Targets and Therapies
Forschungsfeld(er) Allergy
Enabling and Novel Technologies
PSP-Element(e) G-554600-001
G-505400-001
G-503000-001
DOI 10.1126/scitranslmed.aay0605
WOS ID WOS:000528274300006
Scopus ID 85083848414
PubMed ID 32321863
Erfassungsdatum 2020-05-15
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