Evidence map›Paper›PMID 41452432›Full record

ArticleJournal of clinical immunology2025

Age-Related Patterns of Type II Interferon Immunity: Implications for Intramacrophagic Infections and MSMD Diagnosis During Childhood.

Yiyi Luo, Guillermo Argüello, Daniel Acevedo, Cristina Jou, Anna Codina, Jesús Márquez, Alexandru Vlagea, Sara Peiró, Víctor Bolaño, Aina Freixedas and 6 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. Not yet cited in PubMed.

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0cells of the map it votes in
0citing papers in PubMed
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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

16 authors.

Yiyi LuoStudy Group for Immune Dysfunction Diseases in Children (GEMDIP), Institut de Recerca Sant Joan de Déu, Barcelona (IRSJD), Barcelona, EU, Spain. yiyi.luo@sjd.es.
Guillermo ArgüelloMedSavana SL, Madrid, Spain.
Daniel AcevedoStudy Group for Immune Dysfunction Diseases in Children (GEMDIP), Institut de Recerca Sant Joan de Déu, Barcelona (IRSJD), Barcelona, EU, Spain.
Cristina JouBiobank and Pathology department. Institut de Recerca Sant Joan de Déu, Hospital Sant Joan de Déu, CIBERER ISCIII, Barcelona, 08950, Spain.
Anna CodinaBiobank and Pathology department. Institut de Recerca Sant Joan de Déu, Hospital Sant Joan de Déu, CIBERER ISCIII, Barcelona, 08950, Spain.
Jesús MárquezBiobank and Pathology department. Institut de Recerca Sant Joan de Déu, Hospital Sant Joan de Déu, CIBERER ISCIII, Barcelona, 08950, Spain.
Alexandru VlageaClinical Immunology Unit, Hospital Sant Joan de Déu-Hospital Clínic, Barcelona, EU, Spain.
Sara PeiróImmunology Department, Biomedic Diagnostic Center (CDB), Hospital Clínic of Barcelona, Barcelona, Spain.
Víctor BolañoImmunology Department, Biomedic Diagnostic Center (CDB), Hospital Clínic of Barcelona, Barcelona, Spain.
Aina FreixedasStudy Group for Immune Dysfunction Diseases in Children (GEMDIP), Institut de Recerca Sant Joan de Déu, Barcelona (IRSJD), Barcelona, EU, Spain.
Angela Deyà-MartínezStudy Group for Immune Dysfunction Diseases in Children (GEMDIP), Institut de Recerca Sant Joan de Déu, Barcelona (IRSJD), Barcelona, EU, Spain.
Ana García-GarcíaStudy Group for Immune Dysfunction Diseases in Children (GEMDIP), Institut de Recerca Sant Joan de Déu, Barcelona (IRSJD), Barcelona, EU, Spain.
Celia Martí-CastelloteStudy Group for Immune Dysfunction Diseases in Children (GEMDIP), Institut de Recerca Sant Joan de Déu, Barcelona (IRSJD), Barcelona, EU, Spain.
Manel JuanClinical Immunology Unit, Hospital Sant Joan de Déu-Hospital Clínic, Barcelona, EU, Spain.
Ana Esteve-SoléStudy Group for Immune Dysfunction Diseases in Children (GEMDIP), Institut de Recerca Sant Joan de Déu, Barcelona (IRSJD), Barcelona, EU, Spain.
Laia AlsinaStudy Group for Immune Dysfunction Diseases in Children (GEMDIP), Institut de Recerca Sant Joan de Déu, Barcelona (IRSJD), Barcelona, EU, Spain. laia.alsina@sjd.es.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Type II interferon (IFN) immunity is crucial for controlling intramacrophagic infections, driven by the interaction between innate immunity (macrophage-derived IL-12) and adaptive immunity (Th-derived IFN-γ). This study examines the maturation of type II IFN immunity in 55 healthy children (ages 1-18) to enable proper identification of deficiencies as part of the diagnostic evaluation of Mendelian Susceptibility to Mycobacterial Diseases (MSMD). The IL-12/IFN-γ axis was assessed through: (1) cytokine production after mycobacterial stimulation (Luminex and ELISA for IFN-γ, IL-12p70, TNF, CXCL10, IL-1RA, IL-10, IL-1β and IL-6), (2) IFN-γR1/R2 expression on monocytes, and (3) STAT1 phosphorylation/dephosphorylation. T cell maturation (primary IFN-γ source) was evaluated via immunophenotyping (naïve/memory/activated, Th1; Th2; Th17; Th1/17; Tfh) and proliferation assays. Main findings: (1) stable expression/production of key components of the IL-12/IFN-γ axis (IFN-γ, IL-12, TNF, IFN-γR1/2, and STAT1 activity) across ages confirming the stability of innate immune function throughout childhood; (2) increasing responses to IFN-γ with age reflected by increased CXCL10 production, and increase in the IFN-γ counter-acting anti-inflammatory cytokines (IL-10, IL-1RA); and (3) progressive T cell maturation, including Th1, Th17 and Th1/17 subsets, with significant milestones between 6 and 8.6 years, while T cell proliferative capacity remained stable. These observations highlight the stability of IL-12/IFN-γ axis innate components with age, accompanied by enhanced downstream IFN-γ signaling, aligning with the maturation of Th cell compartment. These underscore the limited benefit of age-specific controls in the evaluation of IL-12/IFN-γ axis in MSMD diagnosis, while emphasizing the importance of T cell maturation in the overall type II IFN immunity.

Indexed as

Interferon-gammaMycobacterium InfectionsAdaptive ImmunityAdolescentAge FactorsChildChild, PreschoolCytokinesDisease SusceptibilityFemaleHumansImmunity, InnateImmunophenotypingInfantInterferon gamma ReceptorInterleukin-12CytokinesInterferon-gammaInterferon gamma ReceptorInterleukin-12Receptors, InterferonSTAT1 Transcription FactorCFSEChemokine CXCL10Interferon-gammaPrimary immunodeficiencySTAT1 transcription factorT-lymphocytes

Identifiers

PMID41452432
PMCPMC12831799

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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.