Evidence map›Paper›PMID 42317362›Full record

ArticleFrontiers in immunology2026

Interleukin-15 correlates with cytotoxic immune networks in cervical tuberculous lymphadenitis.

Soumaya Bchiri, Khadija Bahrini, Rosane M B Teles, Ameni Ben Alaya, Houssem Eddine Kamel, Julie West, Kimia Rategh, Asma Bouzekri, Eya Bousalem, Rim Ouni and 13 more

Abstract read
In one paragraph

Article in Frontiers in immunology, 2026. 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

23 authors.

Soumaya BchiriLaboratory of Transmission Control and Immunobiology of Infections, Institut Pasteur de Tunis, Tunis, Tunisia.
Khadija BahriniLaboratory of Transmission Control and Immunobiology of Infections, Institut Pasteur de Tunis, Tunis, Tunisia.
Rosane M B TelesDivision of Dermatology, Department of Medicine, University of California, Los Angeles, Los Angeles, CA, United States.
Ameni Ben AlayaUniversity Tunis El Manar, Tunis, Tunisia.
Houssem Eddine KamelUniversity Tunis El Manar, Tunis, Tunisia.
Julie WestDivision of Dermatology, Department of Medicine, University of California, Los Angeles, Los Angeles, CA, United States.
Kimia RateghDivision of Dermatology, Department of Medicine, University of California, Los Angeles, Los Angeles, CA, United States.
Asma BouzekriLaboratory of Transmission Control and Immunobiology of Infections, Institut Pasteur de Tunis, Tunis, Tunisia.
Eya BousalemLaboratory of Transmission Control and Immunobiology of Infections, Institut Pasteur de Tunis, Tunis, Tunisia.
Rim OuniLaboratory of Transmission Control and Immunobiology of Infections, Institut Pasteur de Tunis, Tunis, Tunisia.
Meriem FassatouiLaboratory of Transmission Control and Immunobiology of Infections, Institut Pasteur de Tunis, Tunis, Tunisia.
Helmi MardassiLaboratory of Molecular Microbiology, Vaccinology and Biotechnological Development, Institut Pasteur de Tunis, Tunis, Tunisia.
Neira DekhilLaboratory of Molecular Microbiology, Vaccinology and Biotechnological Development, Institut Pasteur de Tunis, Tunis, Tunisia.
Issam Ben BelghithLaboratory of Transmission Control and Immunobiology of Infections, Institut Pasteur de Tunis, Tunis, Tunisia.
Rym LahianiUniversity Tunis El Manar, Tunis, Tunisia.
Emna RomdhaneUniversity Tunis El Manar, Tunis, Tunisia.
Meriem Ben-AliLaboratory of Transmission Control and Immunobiology of Infections, Institut Pasteur de Tunis, Tunis, Tunisia.
Soumaya RammehUniversity Tunis El Manar, Tunis, Tunisia.
Asma FerjaniUniversity Tunis El Manar, Tunis, Tunisia.
Mamia Ben-SalehUniversity Tunis El Manar, Tunis, Tunisia.
Mohamed-Ridha BarboucheLaboratory of Transmission Control and Immunobiology of Infections, Institut Pasteur de Tunis, Tunis, Tunisia.
Robert L ModlinDivision of Dermatology, Department of Medicine, University of California, Los Angeles, Los Angeles, CA, United States.
Chaouki BenabdessalemLaboratory of Transmission Control and Immunobiology of Infections, Institut Pasteur de Tunis, Tunis, Tunisia.

Funding

Microbiology and Metagenomics CoreP50AR080594 · NIAMS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI ROBERT L MODLIN · 2022 to 2026
$9.2M
NIAMS NIH HHS P50 AR080594
6 · The paper itself

Abstract

Introduction: Cervical tuberculous lymphadenitis (CTL) represents a localized manifestation of Methods: We performed integrated immune profiling of patients with CTL (n = 60) and non-tuberculous cervical lymphadenopathy (CNTL; n = 44). Immune-gene expression was quantified in peripheral blood and lymph node mononuclear cells by qPCR. Systems-level analyses including principal component and correlation-network approaches were used to define coordinated immune pathways. Serum IL-15 was measured by ELISA, and tissue localization of IL-15 and IL-15Rα was examined by immunohistochemistry. Results: CTL was characterized by a structured cytotoxic immune program enriched for granulysin, granzyme B, perforin, IFN-γ, and CCL5. Network analysis identified IL-15 as a highly connected hub within this cytotoxic module in CTL. IL-15 transcripts were significantly elevated in both blood and lymph node compartments (p = 0.0003; p = 0.0007, respectively) and strongly correlated with cytotoxic effector genes. Circulating IL-15 concentrations were higher in CTL than CNTL (p < 0.0001) and increased with GeneXpert-defined bacillary burden (AUC 0.73). Immunohistochemistry demonstrated IL-15 and IL-15Rα expression within CD68 Conclusions: These findings identify IL-15 as a potential central organizer of cytotoxic immune pathways in CTL and highlight IL-15-linked immune signatures as biologically informative features of CTL immunopathogenesis.

Indexed as

Interleukin-15Mycobacterium tuberculosisT-Lymphocytes, CytotoxicTuberculosis, Lymph NodeAdultCytotoxicity, ImmunologicFemaleHumansLymph NodesMaleMiddle AgedIL15 protein, humanInterleukin-15cervical lymphadenitiscytotoxicityIL-15immunoregulatory markertuberculosis

Identifiers

PMID42317362
PMCPMC13271968

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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.