Evidence map›Paper›PMID 39165363›Full record

ArticleFrontiers in immunology2024

Immune profiling and functional analysis of NK and T cells in ataxia telangiectasia.

Lea Graafen, Annekathrin Heinze, Nawid Albinger, Emilia Salzmann-Manrique, Franziska Ganß, Sabine Hünecke, Claudia Cappel, Sandra Wölke, Helena Donath, Jordis Trischler and 10 more

Abstract read
In one paragraph

Article in Frontiers in immunology, 2024. 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. Article
  2. Review
  3. Review
  4. Article
  5. 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

20 authors.

Lea GraafenDepartment of Pediatrics, Goethe University Frankfurt, Frankfurt am Main, Germany.
Annekathrin HeinzeDepartment of Pediatrics, Goethe University Frankfurt, Frankfurt am Main, Germany.
Nawid AlbingerDepartment of Pediatrics, Goethe University Frankfurt, Frankfurt am Main, Germany.
Emilia Salzmann-ManriqueDepartment of Pediatrics, Goethe University Frankfurt, Frankfurt am Main, Germany.
Franziska GanßDepartment of Pediatrics, Goethe University Frankfurt, Frankfurt am Main, Germany.
Sabine HüneckeDepartment of Pediatrics, Goethe University Frankfurt, Frankfurt am Main, Germany.
Claudia CappelDepartment of Pediatrics, Goethe University Frankfurt, Frankfurt am Main, Germany.
Sandra WölkeDepartment of Pediatrics, Goethe University Frankfurt, Frankfurt am Main, Germany.
Helena DonathDepartment of Pediatrics, Goethe University Frankfurt, Frankfurt am Main, Germany.
Jordis TrischlerDepartment of Pediatrics, Goethe University Frankfurt, Frankfurt am Main, Germany.
Till-Martin TheilenDepartment of Pediatric Surgery and Urology, Goethe University Frankfurt, Frankfurt, Germany.
Christine HellerDepartment of Pediatrics, Goethe University Frankfurt, Frankfurt am Main, Germany.
Christoph KönigsDepartment of Pediatrics, Goethe University Frankfurt, Frankfurt am Main, Germany.
Stephan EhlInstitute for Immunodeficiency, Center for Chronic Immunodeficiency, Medical Center-University of Freiburg, Faculty of Medicine, University of Freiburg, Freiburg, Germany.
Peter BaderDepartment of Pediatrics, Goethe University Frankfurt, Frankfurt am Main, Germany.
Thomas KlingebielDepartment of Pediatrics, Goethe University Frankfurt, Frankfurt am Main, Germany.
Jan-Henning KlusmannDepartment of Pediatrics, Goethe University Frankfurt, Frankfurt am Main, Germany.
Stefan ZielenDepartment of Pediatrics, Goethe University Frankfurt, Frankfurt am Main, Germany.
Ralf SchubertDepartment of Pediatrics, Goethe University Frankfurt, Frankfurt am Main, Germany.
Evelyn UllrichDepartment of Pediatrics, Goethe University Frankfurt, Frankfurt am Main, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Ataxia telangiectasia (AT) is a rare autosomal-recessive disorder characterized by profound neurodegeneration, combined immunodeficiency, and an increased risk for malignant diseases. Treatment options for AT are limited, and the long-term survival prognosis for patients remains grim, primarily due to the emergence of chronic respiratory pathologies, malignancies, and neurological complications. Understanding the dysregulation of the immune system in AT is fundamental for the development of novel treatment strategies. In this context, we performed a retrospective longitudinal immunemonitoring of lymphocyte subset distribution in a cohort of AT patients (

Indexed as

Ataxia TelangiectasiaKiller Cells, NaturalAdolescentAdultChildChild, PreschoolFemaleHumansImmunophenotypingMaleRetrospective StudiesT-LymphocytesYoung Adultataxia telangiectasiaimmune characterizationNK cellsphenotypingT cells

Identifiers

PMID39165363
PMCPMC11333214

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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.