Evidence map›Paper›PMID 35222360›Full record

Observational studyFrontiers in immunology2022

AKT Hyperphosphorylation and T Cell Exhaustion in Down Syndrome.

Daphne Peeters, Ingrid Pico-Knijnenburg, Douwe Wieringa, Mandana Rad, Roos Cuperus, Madelon Ruige, Frank Froeling, Gerda W Zijp, Mirjam van der Burg, Gertjan J A Driessen

Open access · goldAbstract readObservational Study
In one paragraph

Observational study in Frontiers in immunology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.9field-weighted citation impact, top 28% 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

8 citing papers in PubMed, 12 citations in OpenAlex.

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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

10 authors at 3 institutions in 1 country.

Daphne PeetersDepartment of Pediatrics, Juliana Children's Hospital, The Hague, Netherlands.
Ingrid Pico-KnijnenburgDepartment of Pediatrics, Laboratory for Pediatric Immunology, Willem-Alexander Children's Hospital, Leiden University Medical Centre, Leiden, Netherlands.
Douwe WieringaDepartment of Pediatrics, Laboratory for Pediatric Immunology, Willem-Alexander Children's Hospital, Leiden University Medical Centre, Leiden, Netherlands.
Mandana RadDepartment of Pediatric Anaesthesiology, Juliana Children's Hospital/Haga Teaching Hospital, The Hague, Netherlands.
Roos CuperusDepartment of Pediatrics, Juliana Children's Hospital, The Hague, Netherlands.
Madelon RuigeDepartment of Pediatrics, Juliana Children's Hospital, The Hague, Netherlands.
Frank FroelingDepartment of Pediatric Urology, Juliana Children's Hospital, The Hague, Netherlands.
Gerda W ZijpDepartment of Paediatric Surgery, Juliana Children's Hospital, The Hague, Netherlands.
Mirjam van der BurgDepartment of Pediatrics, Laboratory for Pediatric Immunology, Willem-Alexander Children's Hospital, Leiden University Medical Centre, Leiden, Netherlands.
Gertjan J A DriessenDepartment of Pediatrics, Juliana Children's Hospital, The Hague, Netherlands.
Juliana Kinderziekenhuis · NLLeiden University · NLHaga Hospital · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Down syndrome (DS) is associated with increased susceptibility to infections, auto-immunity, immunodeficiency and haematological malignancies. The exact underlying immunological pathophysiology is still unclear. The immunophenotype and clinical characteristics of DS resemble those of Activated PI3K Delta Syndrome (APDS), in which the PI3K/AKT/mTOR pathway is overactivated. We hypothesized that T cell exhaustion and the hyperactivation of the AKT signalling pathway is also present in immune cells of children with DS. In this observational non-interventional cohort study we collected blood samples of children with DS (n=22) and healthy age-matched controls (n=21) for flowcytometric immunophenotyping, phospho-flow AKT analysis and exhaustion analysis of T cells. The median age was 5 years (range 1-12y). Total T and NK cells were similar for both groups, but absolute values and transitional B cells, naive memory B cells and naive CD4+ and CD8+ T cells were lower in DS. pAKT and AKT were increased for CD3+ and CD4+ T cells and CD20+ B cells in children with DS. Total AKT was also increased in CD8+ T cells. Children with DS showed increased expression of inhibitory markers Programmed cell dealth-1 (PD-1), CD244 and CD160 on CD8+ T cells and increased PD-1 and CD244+ expression on CD4+ T cells, suggesting T cell exhaustion. Children with DS show increased pAKT and AKT and increased T cell exhaustion, which might contribute to their increased susceptibility to infections, auto immunity and haematological malignancies.

Indexed as

Down SyndromeProto-Oncogene Proteins c-aktT-LymphocytesChildChild, PreschoolCohort StudiesHematologic NeoplasmsHumansInfantPhosphatidylinositol 3-KinasesProgrammed Cell Death 1 ReceptorPhosphatidylinositol 3-KinasesProgrammed Cell Death 1 ReceptorProto-Oncogene Proteins c-aktactivated PI3 kinase delta syndromeAKT pathwaydown syndromeimmunodeficienciesimmunophenotypingT cell exhaustion

Identifiers

PMID35222360
PMCPMC8866941
OpenAlexW4211029548

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.