Evidence map›Paper›PMID 34531853›Full record

ArticleFrontiers in immunology2021

Case Report:

Afef Rais, Najla Mekki, Faten Fedhila, Mohammed Faraj Alosaimi, Monia Ben Khaled, Amal Zameli, Nourhen Agrebi, Maryam Kallel Sellami, Raif Geha, Imen Ben-Mustapha and 1 more

Open access · goldAbstract readCase Reports
In one paragraph

Article in Frontiers in immunology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.2field-weighted citation impact, top 49% 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

3 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
  2. Review
  3. 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

11 authors at 6 institutions in 3 countries.

Afef RaisLaboratory of Transmission, Control and Immunobiology of Infections (LR11IPT02), Institut Pasteur de Tunis, Tunis, Tunisia.
Najla MekkiLaboratory of Transmission, Control and Immunobiology of Infections (LR11IPT02), Institut Pasteur de Tunis, Tunis, Tunisia.
Faten FedhilaFaculty of Medicine, Université de Tunis El Manar, Tunis, Tunisia.
Mohammed Faraj AlosaimiDepartment of Pediatrics, College of Medicine, King Saud University, Riyadh, Saudi Arabia.
Monia Ben KhaledFaculty of Medicine, Université de Tunis El Manar, Tunis, Tunisia.
Amal ZameliLaboratory of Transmission, Control and Immunobiology of Infections (LR11IPT02), Institut Pasteur de Tunis, Tunis, Tunisia.
Nourhen AgrebiLaboratory of Transmission, Control and Immunobiology of Infections (LR11IPT02), Institut Pasteur de Tunis, Tunis, Tunisia.
Maryam Kallel SellamiFaculty of Medicine, Université de Tunis El Manar, Tunis, Tunisia.
Raif GehaDivision of Immunology, Boston Children's Hospital, Harvard Medical School, Boston, MA, United States.
Imen Ben-MustaphaLaboratory of Transmission, Control and Immunobiology of Infections (LR11IPT02), Institut Pasteur de Tunis, Tunis, Tunisia.
Mohamed-Ridha BarboucheLaboratory of Transmission, Control and Immunobiology of Infections (LR11IPT02), Institut Pasteur de Tunis, Tunis, Tunisia.
Institut Pasteur de Tunis · TNTunis University · TNTunis El Manar University · TNChildren's Hospital · TNHarvard University · USKing Saud University · SA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

ALPS and IPEX are two well-characterized inborn errors of immunity with immune dysregulation, considered as two master models of monogenic auto-immune diseases. Thus, with autoimmunity as their primary clinical manifestation, these two entities may show clinical overlap. Traditionally, immunological biomarkers are used to establish an accurate differential diagnosis. Herein, we describe a patient who presented with clinical features and biomarkers fulfilling the diagnostic criteria of ALPS. Severe apoptotic defect was also shown in the patient's cell lines and PHA-activated peripheral blood lymphocytes. Sanger sequencing of the

Indexed as

Autoimmune Lymphoproliferative SyndromeChildForkhead Transcription FactorsHumansMaleMutationForkhead Transcription FactorsFOXP3 protein, humanALPSFOXP3inborn errors of immunityIPEXNGS

Identifiers

PMID34531853
PMCPMC8438314
OpenAlexW3197408987

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.