Evidence map›Paper›PMID 41026241›Full record

ArticleJournal of clinical immunology2025

Malignancy and Autoimmune Susceptibility in Adult Patients with Human Inborn Errors of Immunity.

Alejandro Segura-Tudela, Celia Nieto-López, Francisco Javier Bermejo-Olivera, Luis A Andara, Javier Arroyo-Ródenas, Lucía Dueñas-Prieto, Ángel Alfocea-Molina, Estela Paz-Artal, Daniel Pleguezuelo, Oscar Cabrera-Marante and 1 more

Abstract read
In one paragraph

Article in Journal of clinical immunology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

11 authors.

Alejandro Segura-Tudela *Department of Immunology, University Hospital 12 de Octubre, Madrid, Spain.
Celia Nieto-López *Department of Immunology, University Hospital 12 de Octubre, Madrid, Spain.
Francisco Javier Bermejo-OliveraDepartment of Immunology, University Hospital 12 de Octubre, Madrid, Spain.
Luis A AndaraDepartment of Immunology, University Hospital 12 de Octubre, Madrid, Spain.
Javier Arroyo-RódenasDepartment of Immunology, University Hospital 12 de Octubre, Madrid, Spain.
Lucía Dueñas-PrietoDepartment of Immunology, University Hospital 12 de Octubre, Madrid, Spain.
Ángel Alfocea-MolinaDepartment of Immunology, University Hospital 12 de Octubre, Madrid, Spain.
Estela Paz-ArtalDepartment of Immunology, University Hospital 12 de Octubre, Madrid, Spain.
Daniel PleguezueloDepartment of Immunology, University Hospital 12 de Octubre, Madrid, Spain.
Oscar Cabrera-MaranteDepartment of Immunology, University Hospital 12 de Octubre, Madrid, Spain.
Luis M AllendeDepartment of Immunology, University Hospital 12 de Octubre, Madrid, Spain. luis.allende@salud.madrid.org.

Funding

Instituto de Salud Carlos III PI21/01119Private project 21/132
6 · The paper itself

Abstract

Inborn errors of immunity (IEI) are a heterogeneous group of genetic disorders that disrupt the normal development and function of the immune system. These diseases not only increase susceptibility to infections but also significantly elevate the risk of developing malignancies and autoimmune diseases. The interplay between immune dysregulation, chronic inflammation, and altered cellular homeostasis in IEI can lead to aberrant cellular proliferation and self-reactive immune responses. Malignancy in IEI often arises due to the immune system's failure to effectively eliminate transformed cells, predisposing patients to lymphomas, leukemias and solid tumors. Autoimmune diseases in IEI can result from defective T-regulatory cell function, impaired central or peripheral tolerance mechanisms or B-cell dysregulation leading to autoantibody production. This work was a retrospective study of 173 adults with IEI suspicion who underwent genetic sequencing between 2005 and 2023. A significant increase of malignancies was observed in patients with a molecular diagnosis (w_MolDx) compared to those without (wo_MolDx). Notably, hematologic malignancies were predominant in the w_MolDx cohort, whereas solid tumors were more frequently observed in the wo_MolDx group. In contrast, the correlation between autoimmune diseases and molecular diagnosis was less evident when comparing w_MolDx and wo_MolDx patients. Understanding the complex relationship between IEI, malignancies and autoimmunity is crucial for optimizing patient management. Early diagnosis of IEI allows for timely interventions, including hematopoietic stem cell transplantation, gene therapy and targeted immunomodulatory therapies, which can mitigate the risk of both malignancies and autoimmune complications.

Indexed as

Autoimmune DiseasesNeoplasmsAdolescentAdultAgedAutoimmunityDisease SusceptibilityFemaleGenetic Predisposition to DiseaseHumansMaleMiddle AgedRetrospective StudiesYoung AdultALPS-likeAutoimmune lymphoproliferative syndrome (ALPS)Immune dysregulationJeffrey model foundation (JMF) warning signsLymphoproliferationPrimary immune regulatory disorders (PIRD)

Identifiers

PMID41026241
PMCPMC12484250

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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.