Evidence map›Paper›PMID 37753823›Full record

ArticleThe clinical respiratory journal2023

Deconvolution of bulk RNA sequencing in activated phosphoinositide 3-kinase δ syndrome.

Xia Huang, Haiyan Gu

Open access · goldAbstract read
In one paragraph

Article in The clinical respiratory journal, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.2field-weighted citation impact, top 38% 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

2 citing papers in PubMed, 1 citations in OpenAlex.

  1. 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

2 authors at 1 institution in 1 country.

Xia HuangDepartment of Respiratory Medicine, Children's Hospital of Nanjing Medical University, Nanjing, China.
Haiyan GuDepartment of Respiratory Medicine, Children's Hospital of Nanjing Medical University, Nanjing, China.ORCID https://orcid.org/0000-0002-7013-3955
Nanjing Children's Hospital · CN

Funding

National Natural Science Foundation of China 82200008
6 · The paper itself

Abstract

backgroundMany gaps remain in our understanding of the immune and molecular characteristics that underlie activated phosphoinositide 3-kinase delta syndrome (APDS).

methodsWe performed RNA sequencing of peripheral blood leukocytes obtained from a child with APDS and his healthy parents and deconvoluted bulk transcriptional data to assess immune cell status.

resultsPathway enrichment analysis suggested signaling pathways enriched in virus infection as well as the PI3K, mitogen-activated protein kinase (MAPK), natural killer cell-mediated cytotoxicity, and nucleotide-binding oligomerization domain (NOD)-like receptor signaling pathways. The proportion of B cells memory, T cells CD4 memory resting and dendritic cells activated were reduced, whereas B cells naïve, T cells CD8, NK cells resting, monocytes and macrophages M2 were increased in the child. Top 10 hub genes were screened and showed moderate to strong relatedness with immune cell proportions.

conclusionDeconvolution of bulk RNA sequencing to assess immune cells status can provide further insight into the alterations in immunological features underlying APDS and other rare diseases.

Indexed as

Immunologic Deficiency SyndromesPhosphatidylinositol 3-KinaseChildClass I Phosphatidylinositol 3-KinasesHumansPhosphatidylinositol 3-KinasesSignal TransductionClass I Phosphatidylinositol 3-KinasesPhosphatidylinositol 3-KinasePhosphatidylinositol 3-KinasesCIBERSORTPI3Kδprimary immunodeficiencyRNA-seq

Identifiers

PMID37753823
PMCPMC10632076
OpenAlexW4387077348

What OpenQuestion holds

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Registered trials

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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.