Jonathan Brestoff

Jonathan Brestoff

orcid

Research Focus & Metrics

Academic Career Length

19Years (2008-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 September 2017 in Cell
Verified
Journal Article
Closed access
LOLandon K. Oetjen
Landon K. Oetjen
MMMadison R. Mack
Madison R. Mack
JFJing Feng
Jing Feng
TWTimothy M. Whelan
Timothy M. Whelan
HNHaixia Niu
Haixia Niu
BKBrian S. Kim
Brian S. Kim

22 December 2014 in Nature
Verified
Journal Article
Closed access
PDF file
JBJonathan Brestoff
Jonathan Brestoff
BKBrian S. Kim
Brian S. Kim
SSSteven A. Saenz
Steven A. Saenz
RSRachel R. Stine
Rachel R. Stine
LMLaurel A. Monticelli
Laurel A. Monticelli
DADavid Artis
David Artis

18 June 2013 in Nature Immunology
Verified
Journal Article
Closed access
PDF file
JBJonathan Brestoff
Jonathan Brestoff
DADavid Artis
David Artis

8 November 2023 in Nature
Verified
Journal Article
Closed access
PDF file
NBNicholas Borcherding
Nicholas Borcherding
JBJonathan Brestoff
Jonathan Brestoff

1 March 2015 in Cell
Verified
Journal Article
Closed access
JBJonathan Brestoff
Jonathan Brestoff
DADavid Artis
David Artis

2 March 2018 in Science
Verified
Journal Article
Closed access
PDF file
SMSaya Moriyama
Saya Moriyama
JBJonathan Brestoff
Jonathan Brestoff
AFAnne-Laure Flamar
Anne-Laure Flamar
JMJesper Bonnet Moeller
Jesper Bonnet Moeller
CKChristoph S. N. Klose
Christoph S. N. Klose
DADavid Artis
David Artis
An off switch for helminth immunity: Group 2 innate lymphoid cells (ILC2s) are involved in responses to helminths, viruses, and allergens. Moriyamaet al.found that ILC2s interact with the nervous system to modulate helminth immunity. ILC2s from the small intestine expressed the β2-adrenergic receptor (β2AR), which normally interacts with the neurotransmitter epinephrine. Inactivating β2AR resulted in lower helminth burden and more ILC2s, eosinophils, and type 2 cytokine production in mice. Conversely, treatment of helminth-infected mice with a β2AR agonist enhanced worm burden and reduced proliferation of ILC2s. Thus, β2AR negatively regulates ILC2-driven protective immunity.Science, this issue p.1056