Evidence map›Paper›PMID 41620725›Full record

ArticleBMC pulmonary medicine2026

Demographic, clinical, and immunological features in combined immunodeficiency patients: a comparative analysis of those with and without pulmonary manifestations - a multicenter study from Iran.

Ghamartaj Khanbabaee, Matin Pourghasem, Mahnaz Jamee, Seyed Ahmad Tabatabaii, Mitra Khalili, Samin Sharafian, Mehrnaz Mesdaghi, Mahnaz Sadeghi-Shabestari, Armin Shirvani, Saeid Sadr and 15 more

Abstract readMulticenter StudyComparative Study
In one paragraph

Article in BMC pulmonary medicine, 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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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

25 authors.

Ghamartaj Khanbabaee *Department of Pediatric Pulmonology, Mofid Children's Hospital, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Matin Pourghasem *Pediatric Diseases Research Center, Guilan university of Medical Sciences, Rasht, Iran. Matinpourghasem@yahoo.com.
Mahnaz JameePediatric Nephrology Research Center, Research Institute for Children's Health, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Seyed Ahmad TabatabaiiDepartment of Pediatric Pulmonology, Mofid Children's Hospital, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Mitra KhaliliDepartment of Radiology, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Samin SharafianImmunology and Allergy Department, Mofid Children's Hospital, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Mehrnaz MesdaghiImmunology and Allergy Department, Mofid Children's Hospital, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Mahnaz Sadeghi-ShabestariImmunology Research Center of Tabriz, TB and lung research center of Tabriz, children hospital, Tabriz University of medical science, Tabriz, Iran.
Armin ShirvaniDepartment of Medical Education, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Saeid SadrDepartment of Pediatric Pulmonology, Mofid Children's Hospital, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Arefeh ZahmatkeshPediatric Nephrology Research Center, Research Institute for Children's Health, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Samaneh DelavariResearch Center for Immunodeficiencies, Pediatrics Center of Excellence, Children's Medical Center, Tehran University of Medical Sciences, Tehran, Iran.
Narges EslamiImmunology and Allergy Department, Mofid Children's Hospital, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Nazanin FarahbakhshDepartment of Pediatric Pulmonology, Mofid Children's Hospital, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Mahboubeh MansouriImmunology and Allergy Department, Mofid Children's Hospital, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Ebrahim TabieiDepartment of Pediatric Pulmonology, Akbar Children's Hospital, Mashhad University of Medical Sciences, Mashhad, Iran.
Seyedeh Zalfa ModarresiChildren Growth Disorder Research Center, Shahid Sadoughi University of Medical Sciences, Yazd, Iran.
Abdolhamid Taghizadeh BehbahaniDepartment of Pediatric Cardiology, Cardiovascular Research center, Rajaie cardiovascular institute, Tehran, Iran.
Golnaz EslamianImmunology and Allergy Department, Mofid Children's Hospital, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Mazdak FallahiShahid fahmideh children hospital, Iran University of medical sciences, Tehran, Iran.
Javad EnayatDepartment of Pediatrics, Taleghani Children's Hospital, Golestan University of Medical Sciences, Gorgan, Iran.
Shahrzad FallahImmunology and Allergy Department, Mofid Children's Hospital, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Mahsa PourghasemDepartment of Pharmacy, Pharmaceutical Sciences Branch (IAUPS), Islamic Azad University, Tehran, Iran.
Asghar AghamohammadiResearch Center for Immunodeficiencies, Pediatrics Center of Excellence, Children's Medical Center, Tehran University of Medical Sciences, Tehran, Iran.
Zahra ChavoshzadehImmunology and Allergy Department, Mofid Children's Hospital, Shahid Beheshti University of Medical Sciences, Tehran, Iran. zahra_chavoshzadeh@yahoo.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCombined immunodeficiency (CID) involves profound defects in B and T lymphocyte development and function. This study examined clinical and immunological phenotypes of CID patients with and without pulmonary manifestations.

methodsThis retrospective multicenter study included 53 CID patients diagnosed between 2009 and 2022 with available thoracic computed tomography scans. Patients were categorized based on pulmonary manifestations presence. Demographic, clinical, and laboratory characteristics were compared using conservative statistical thresholds (P < 0.01). All laboratory parameters were interpreted using age-adjusted pediatric reference ranges.

resultsAmong 53 patients (56.6% male), 43 had pulmonary abnormalities on HRCT. Common clinical features included skin lesions (43.4%), failure to thrive (34%), and autoimmunity (32.1%). HRCT revealed pneumonia (28.3%), bronchiectasis (18.9%), interstitial lung disease with BOOP-like pattern (3.8%), and other findings. Using age-adjusted pediatric reference ranges, profound immunological defects were confirmed: absolute lymphocyte count below the 5th percentile in 92% (49/53), CD3 + T cells below the 5th percentile in 94% (47/50 tested), CD4 + T cells below the 5th percentile in 96% (51/53), CD19 + B cells below the 5th percentile in 94% (50/53), and hypogammaglobulinaemia (IgG below the 5th percentile) in 98% (52/53). Patients with abnormal HRCT had significantly lower CD4 + T-cell counts (178 vs. 498 cells/µL; P = 0.008) and CD19 + B-cell counts (42 vs. 189 cells/µL; P = 0.009). Bronchoscopy identified Aspergillus fumigatus, Streptococcus pneumoniae, and multidrug-resistantAcinetobacter baumannii. Deceased patients showed significantly lower baseline platelets (183,000 vs. 266,000 cells/µL; P = 0.009), IgG (380 vs. 720 mg/dL; P = 0.007), and IgE (0.8 vs. 12 IU/mL; P = 0.008).

conclusionPulmonary manifestations affect 81.1% of Iranian CID patients. Low baseline platelets, IgG, and IgE constitute a robust prognostic triad for mortality (P = 0.009, P = 0.007, P = 0.008 respectively). Application of age-adjusted reference ranges revealed profound immunological defects. Systematic HRCT surveillance using low-dose protocols and distinguishing infectious sequelae from immune-mediated lung disease guides targeted management in resource-limited settings.

Indexed as

Lung Diseases, InterstitialSevere Combined ImmunodeficiencyBronchiectasisChildChild, PreschoolFemaleHumansInfantIranLymphocyte CountMaleRetrospective StudiesTomography, X-Ray ComputedBronchiectasisCombined immunodeficiencyHRCTInterstitial lung diseasePrimary immunodeficiencyPrognostic biomarkersPulmonary manifestations

Identifiers

PMID41620725
PMCPMC12947537

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