Evidence map›Paper›PMID 33569778›Full record

ReviewEuropean journal of immunology2021

Multiomics uncovers developing immunological lineages in human.

Emily Stephenson, Simone Webb, Muzlifah Haniffa

Abstract readReview
In one paragraph

Review in European journal of immunology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
  4. Review
  5. Review
  6. Resolving trained immunity with systems biology.European journal of immunology · 2021
    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.

Emily StephensonBiosciences Institute, Newcastle University, Newcastle Upon Tyne, NE2 4HH, UK.
Simone WebbBiosciences Institute, Newcastle University, Newcastle Upon Tyne, NE2 4HH, UK.
Muzlifah HaniffaBiosciences Institute, Newcastle University, Newcastle Upon Tyne, NE2 4HH, UK.

Funding

Department of HealthWellcome TrustWellcome Trust WT107931/Z/15/ZWellcome Trust WT211276/Z/18/Z
6 · The paper itself

Abstract

The development of the human immune system during embryonic and fetal life has historically been difficult to research due to limited access to human tissue. Experimental animal models have been widely used to study development but cellular and molecular programmes may not be conserved across species. The advent of multiomic single-cell technologies and an increase in human developmental tissue biobank resources have facilitated single-cell multiomic studies focused on human immune development. A critical question in the near future is "How do we best reconcile scientific findings across multiple omic modalities, developmental time, and organismic space?" In this review, we discuss the application of single-cell multiomic technologies to unravel the major cellular lineages in the prenatal human immune system. We also identify key areas where the combined power of multiomics technologies can be leveraged to address specific immunological gaps in our current knowledge and explore new research horizons in human development.

Indexed as

Cell LineageEmbryo, MammalianEmbryonic DevelopmentEpigenomicsGene Expression ProfilingGenomicsHigh-Throughput Nucleotide SequencingHumansProteomicsSingle-Cell Analysisbioinformaticsdevelopmental immunologyprenatal immunity

Identifiers

PMID33569778
PMCPMC8600952

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.