Evidence map›Paper›PMID 32117280›Full record

ArticleFrontiers in immunology2020

An Anti-inflammatory microRNA Signature Distinguishes Group 3 Innate Lymphoid Cells From Natural Killer Cells in Human Decidua.

Andrea Pelosi, Claudia Alicata, Nicola Tumino, Tiziano Ingegnere, Fabrizio Loiacono, Maria Cristina Mingari, Lorenzo Moretta, Paola Vacca

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.4field-weighted citation impact, top 19% 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

13 citing papers in PubMed, 21 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. ILC3: a case of conflicted identity.Frontiers in immunology · 2023
    Review
  6. Article
  7. Review
  8. Article
  9. Review
  10. Review
  11. miRNAs in decidual NK cells: regulators worthy of attention during pregnancy.Reproductive biology and endocrinology : RB&E · 2021
    Review
  12. Deciphering the role of microRNAs in mustard gas-induced toxicity.Annals of the New York Academy of Sciences · 2021
    Review
  13. Article
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

8 authors at 3 institutions in 1 country.

Andrea PelosiImmunology Research Area, IRCCS Bambino Gesù Pediatric Hospital, Rome, Italy.
Claudia AlicataImmunology Research Area, IRCCS Bambino Gesù Pediatric Hospital, Rome, Italy.
Nicola TuminoImmunology Research Area, IRCCS Bambino Gesù Pediatric Hospital, Rome, Italy.
Tiziano IngegnereImmunology Research Area, IRCCS Bambino Gesù Pediatric Hospital, Rome, Italy.
Fabrizio LoiaconoImmunology Operative Unit, Department of Integrated Oncological Therapies, IRCCS Policlinico San Martino Hospital, Genoa, Italy.
Maria Cristina MingariImmunology Operative Unit, Department of Integrated Oncological Therapies, IRCCS Policlinico San Martino Hospital, Genoa, Italy.
Lorenzo MorettaImmunology Research Area, IRCCS Bambino Gesù Pediatric Hospital, Rome, Italy.
Paola VaccaImmunology Research Area, IRCCS Bambino Gesù Pediatric Hospital, Rome, Italy.
Bambino Gesù Children's Hospital · ITIstituti di Ricovero e Cura a Carattere Scientifico · ITOspedale Policlinico San Martino · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Innate lymphoid cells (ILCs) are a heterogeneous subset of lymphocytes deeply implicated in the innate immune responses to different pathogens, in lymphoid organogenesis and in the maintenance of tissue homeostasis. Group 3 innate lymphoid cells (ILC3) have been detected in human decidua, where they play a role in the early inflammatory phase favoring implantation and tissue remodeling as well as in the subsequent regulatory phase preventing fetal rejection and supporting neoangiogenesis. A balance between inflammation and immune tolerance is required to maintain pregnancy, thus maternal immune system must be controlled by finely tuned mechanisms. microRNAs (miRNAs) are small non-coding RNAs with important regulatory roles in immune cells, but their function in decidual ILC3 (dILC3) and in decidual NK (dNK) cells is still undefined. Here, we examined the miRNome by microarray in these cells during the first trimester of pregnancy and compared with miRNA profiles of peripheral blood NK (pbNK) cells from pregnant women. We show that distinct miRNA profiles could clearly distinguish dILC3 from NK cells. Correlation analyses revealed that dNK and pbNK miRNome profiles are more similar to each other as compared to dILC3. In particular, we identified 302 and 279 mature miRNAs differentially expressed in dILC3 as compared to dNK and pbNK, respectively. The expression of

Indexed as

Immunity, InnateTranscriptomeCells, CulturedDeciduaFemaleGene Expression ProfilingGene Expression RegulationHumansImmune ToleranceInflammationKiller Cells, NaturalMicroRNAsPregnancyPregnancy Trimester, FirstPrincipal Component AnalysisReal-Time Polymerase Chain ReactionMicroRNAsdeciduaILC3innate lymphoid cellsmicroRNANK cells

Identifiers

PMID32117280
PMCPMC7015979
OpenAlexW3005130261

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.