Evidence map›Paper›PMID 26093676›Full record

ReviewTrends in immunology2015

Innate immunity at mucosal surfaces: the IRE1-RIDD-RIG-I pathway.

Wayne I Lencer, Heidi DeLuca, Michael J Grey, Jin Ah Cho

Open access · greenAbstract readReview
In one paragraph

Review in Trends in immunology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
2.5field-weighted citation impact, top 11% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

30 citing papers in PubMed, 49 citations in OpenAlex.

  1. Article
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  3. Article
  4. Article
  5. Aging · 2023
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  6. Article
  7. Review
  8. Review
  9. Review
  10. Article
  11. Review
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  14. Crosstalk between ER stress, NLRP3 inflammasome, and inflammation.Applied microbiology and biotechnology · 2020
    Review
  15. Article
  16. Review
  17. Article
  18. Review
  19. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors at 1 institution in 1 country.

Wayne I LencerDepartment of Pediatrics, Harvard Medical School and Boston Children's Hospital, Boston, MA, USA; Harvard Digestive Diseases Center, Boston, MA, USA. Electronic address: Wayne.Lencer@childrens.harvard.edu.
Heidi DeLucaDepartment of Pediatrics, Harvard Medical School and Boston Children's Hospital, Boston, MA, USA.
Michael J GreyDepartment of Pediatrics, Harvard Medical School and Boston Children's Hospital, Boston, MA, USA.
Jin Ah ChoDepartment of Pediatrics, Harvard Medical School and Boston Children's Hospital, Boston, MA, USA; Harvard Digestive Diseases Center, Boston, MA, USA.
Boston Children's Hospital · US

Funding

STRUCTURE-FUNCTION RELATIONSHIPS IN THE ALIMENTARY TRACTP30DK034854 · NIDDK · HARVARD UNIVERSITY (MEDICAL SCHOOL) · PI WAYNE I LENCER · 1986 to 2026
$32.4M
Mechanism of action for the epithelial-specific ER stress sensor IRE1β in regulating intestinal homeostasis and host defenseR01DK048106 · NIDDK · CHILDREN'S HOSPITAL BOSTON · PI WAYNE I LENCER · 1993 to 2026
$9.6M
Intestinal Disease-enterocyte toxin interactionR37DK048106 · NIDDK · BOSTON CHILDREN'S HOSPITAL · PI LENCER, WAYNE I · 2011 to 2020
$7.0M
FcRn-dependent sorting of IgG and IgG-opsinized antigens by epithelial cellsR01DK084424 · NIDDK · BOSTON CHILDREN'S HOSPITAL · PI LENCER, WAYNE I · 2009 to 2013
$1.9M
Intestinal innate immunity by the IRE1-RIDD pathwayK01DK102828 · NIDDK · BOSTON CHILDREN'S HOSPITAL · PI CHO, JIN AH · 2015 to 2015
$154k
NIDDK NIH HHS DK048106NIDDK NIH HHS DK084424NIDDK NIH HHS K01 DK102828NIDDK NIH HHS P30 DK034854NIDDK NIH HHS R01 DK048106NIDDK NIH HHS R01 DK084424NIDDK NIH HHS R37 DK048106
6 · The paper itself

Abstract

Recent studies have linked the ER stress sensor IRE1α with the RIG-I pathway, which triggers an inflammatory response upon detection of viral RNAs. In response to ER dysfunction, IRE1α cleaves mRNA into single-strand fragments that lack markers of self, which activate RIG-I. Certain microbial products from mucosal pathogens activate this pathway by binding IRE1α directly, and the discovery that IRE1 is amplified at mucosal surfaces by gene duplication suggests an important role for IRE1 in mucosal immunity. Here, we review evidence in support of this hypothesis, and propose a model wherein IRE1 surveys the integrity of the ER, acting as a guard receptor and a pattern recognition receptor, capable both of sensing cellular stress caused by microbial infection and of responding to pathogens directly.

Indexed as

Immunity, InnateImmunity, MucosalDEAD Box Protein 58DEAD-box RNA HelicasesEndoplasmic ReticulumEndoribonucleasesHumansMucous MembraneProtein Serine-Threonine KinasesReceptors, ImmunologicSurface PropertiesDEAD Box Protein 58DEAD-box RNA HelicasesEndoribonucleasesERN1 protein, humanProtein Serine-Threonine KinasesReceptors, ImmunologicRIGI protein, humaninflammationinnate immunityintestineIRE1mucosal immunityRIG-I

Identifiers

PMID26093676
PMCPMC4490948
OpenAlexW1573568265

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.