Evidence map›Paper›PMID 41977281›Full record

ArticleInternational journal of molecular sciences2026

Myxovirus Resistance A Protein Expression in Idiopathic Inflammatory Myopathies and Hereditary Muscle Diseases with Inflammatory Cell Infiltration: A North African Study.

Emna Farhat, Imen Zamali, Thouraya Ben Younes, Hedia Klaa, Werner Stenzel, Samar Samoud, Hanen Ben Rhouma, Yousr Galai, Ilhem Ben Youssef-Turki, Ichraf Kraoua and 2 more

Abstract read
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Article in International journal of molecular sciences, 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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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

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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

12 authors.

Emna FarhatFaculty of Medicine of Tunis, Tunis El Manar University, Tunis 1007, Tunisia.ORCID 0009-0004-3431-4566
Imen ZamaliFaculty of Medicine of Tunis, Tunis El Manar University, Tunis 1007, Tunisia.ORCID 0000-0002-0438-6807
Thouraya Ben YounesFaculty of Medicine of Tunis, Tunis El Manar University, Tunis 1007, Tunisia.
Hedia KlaaFaculty of Medicine of Tunis, Tunis El Manar University, Tunis 1007, Tunisia.
Werner StenzelDepartment of Neuropathology, Charité Medicine University, 10117 Berlin, Germany.
Samar SamoudLaboratory of the Transmission, Control and Immunobiology of Infections, Pasteur Institute, Tunis 1002, Tunisia.ORCID 0009-0003-0652-6484
Hanen Ben RhoumaFaculty of Medicine of Tunis, Tunis El Manar University, Tunis 1007, Tunisia.
Yousr GalaiDepartment of Clinical Immunology, Pasteur Institute of Tunis, Tunis 1002, Tunisia.
Ilhem Ben Youssef-TurkiFaculty of Medicine of Tunis, Tunis El Manar University, Tunis 1007, Tunisia.
Ichraf KraouaFaculty of Medicine of Tunis, Tunis El Manar University, Tunis 1007, Tunisia.
Mélika Ben AhmedFaculty of Medicine of Tunis, Tunis El Manar University, Tunis 1007, Tunisia.
Ahlem Ben HmidFaculty of Medicine of Tunis, Tunis El Manar University, Tunis 1007, Tunisia.ORCID 0000-0001-9766-920X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Muscle biopsy (MB) is an important tool to help differentiate idiopathic inflammatory myopathies (IIMs) from hereditary muscular diseases (HMDs). The usefulness of immunohistochemical stains of the major histocompatibility complex class I and the membrane attack complex are controversial, as both may be identified in some HMDs. More sensitive markers of IIMs have recently been used, such as myxovirus resistance A (MxA), a type I interferon-inducible protein. We selected skeletal MB samples from 81 patients diagnosed with IIM and HMD harbouring overt inflammatory infiltrates on their MBs in the period between March 2022 and September 2024. Two groups were identified: the IIM group (46 cases) and the HMD group (35 cases). We characterized and compared the patterns of MxA protein expression among the two groups. In the IIM group, positive sarcoplasmic MxA expression was detected on the myofibres of 10 patients (24%), among whom were eight dermatomyositis patients. In the HMD group, we did not identify any sarcoplasmic positivity. However, five patients (14%) showed positive labelling restricted to the sarcolemmal membrane, including non-necrotic or regenerating fibres. Our study demonstrates the value of MxA for increasing dermatomyositis diagnostic accuracy and suggests the potential role of interferon type I in the pathophysiology of HMD.

Indexed as

Muscular DiseasesMyositisMyxovirus Resistance ProteinsAdolescentAdultAgedFemaleHumansMaleMiddle AgedMuscle, SkeletalYoung AdultMX1 protein, humanMyxovirus Resistance Proteinsimmune systemimmunohistochemistryinflammatory myopathiesmuscle biopsymuscular dystrophiesmyxovirus resistance Atype I interferon

Identifiers

PMID41977281
PMCPMC13073650

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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.