Evidence map›Paper›PMID 36838426›Full record

ReviewMicroorganisms2023

Innate Lymphoid Cell Plasticity in Mucosal Infections.

Anna A Korchagina, Ekaterina Koroleva, Alexei V Tumanov

Abstract readReview
In one paragraph

Review in Microorganisms, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
–field-weighted citation impact
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

15 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Review
  6. Review
  7. Review
  8. Review
  9. Progesterone amplifies allergic inflammation and airway pathology in association with higher lung ILC2 responses.American journal of physiology. Lung cellular and molecular physiology · 2024
    Article
  10. Review
  11. Review
  12. Review
  13. Review
  14. Transcriptional control of ILC identity.Frontiers in immunology · 2023
    Review
  15. Review
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

3 authors.

Anna A KorchaginaDepartment of Microbiology, Immunology and Molecular Genetics, University of Texas Health Science Center at San Antonio, 7703 Floyd Curl Dr., San Antonio, TX 78229, USA.ORCID 0000-0001-6177-2379
Ekaterina KorolevaDepartment of Microbiology, Immunology and Molecular Genetics, University of Texas Health Science Center at San Antonio, 7703 Floyd Curl Dr., San Antonio, TX 78229, USA.
Alexei V TumanovDepartment of Microbiology, Immunology and Molecular Genetics, University of Texas Health Science Center at San Antonio, 7703 Floyd Curl Dr., San Antonio, TX 78229, USA.ORCID 0000-0001-6042-0152

Funding

Lymphotoxin-Beta Receptor Peripheral Signaling Regulates the Transition to Inflammation and Neuropathy-Induced Chronic PainR01NS112263 · NINDS · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI AKOPIAN, ARMEN N, TUMANOV, ALEXEI V · 2020 to 2024
$2.4M
Novel animal models to study organ-specific SARS-CoV-2-induced pathologyR21AI173816 · NIAID · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI KOROLEVA, EKATERINA, MARTINEZ-SOBRIDO, LUIS · 2023 to 2024
$499k
Innate lymphoid cells in Campylobacter-induced colitisR21AI135574 · NIAID · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI TUMANOV, ALEXEI V · 2018 to 2019
$419k
Targeting SARS-CoV-2 induced lung immunopathology using novel genetic mouse modelsR21AI161400 · NIAID · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI KOROLEVA, EKATERINA, TUMANOV, ALEXEI V · 2022 to 2023
$419k
NIAID NIH HHS R21 AI135574NIAID NIH HHS R21 AI161400NIAID NIH HHS R21 AI173816NIH HHS AI135574, AI161400, AI173816NINDS NIH HHS R01 NS112263
6 · The paper itself

Abstract

Mucosal tissue homeostasis is a dynamic process that involves multiple mechanisms including regulation of innate lymphoid cells (ILCs). ILCs are mostly tissue-resident cells which are critical for tissue homeostasis and immune response against pathogens. ILCs can sense environmental changes and rapidly respond by producing effector cytokines to limit pathogen spread and initiate tissue recovery. However, dysregulation of ILCs can also lead to immunopathology. Accumulating evidence suggests that ILCs are dynamic population that can change their phenotype and functions under rapidly changing tissue microenvironment. However, the significance of ILC plasticity in response to pathogens remains poorly understood. Therefore, in this review, we discuss recent advances in understanding the mechanisms regulating ILC plasticity in response to intestinal, respiratory and genital tract pathogens. Key transcription factors and lineage-guiding cytokines regulate this plasticity. Additionally, we discuss the emerging data on the role of tissue microenvironment, gut microbiota, and hypoxia in ILC plasticity in response to mucosal pathogens. The identification of new pathways and molecular mechanisms that control functions and plasticity of ILCs could uncover more specific and effective therapeutic targets for infectious and autoimmune diseases where ILCs become dysregulated.

Indexed as

ILC plasticityinnate lymphoid cellsmucosal pathogens

Identifiers

PMID36838426
PMCPMC9967737

What OpenQuestion holds

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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.