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Published on: February 22, 2020
Decreased Natural Killer Cells in Mucormycosis
Alejandra Albarrán-Sánchez1, Maura E Noyola-García1, Luis M Borges-López1
1Medicina Interna, Unidad Médica de Alta Especialidad Hospital de Especialidades, Dr. Bernardo Sepúlveda, Centro Médico Nacional Siglo XXI, Instituto Mexicano del Seguro Social, Mexico City, Mexico.
Background:
Mucormycosis is an invasive fungal infection associated with high morbidity and mortality rates. Previous in vitro studies have demonstrated functional abnormalities in natural killer (NK) cells; however, it remains unclear whether circulating NK cell counts are altered in affected patients.
Aim:
To assess baseline NK cell counts and explore their clinical associations in patients with mucormycosis treated at a tertiary referral hospital in Mexico City.
Methods:
We conducted a cross-sectional analytical study of hospitalized patients with active mucormycosis, as confirmed by direct tissue examination and culture, at the Hospital de Especialidades, Centro Médico Nacional Siglo XXI. From 2019-2024, we performed peripheral blood immunophenotyping and obtained sociodemographic, clinical, and biochemical data. Non-parametric tests were used to compare NK cell counts across clinical subgroups.
Results:
We included 34 patients (59% male; median age, 59 years). Rhino-orbital-cerebral mucormycosis was the most frequent presentation. The most common comorbidities were diabetes (85.3%), hypertension (64.7%), and chronic kidney disease (8.8%). Poor glycemic control (79.4%), prior corticosteroid use (38.2%), previous COVID-19 infection (26.5%), and solid cancer (5.9%) were the main risk factors. Compared with the reference range patients showed reduced NK cell counts (median 0.11 [IQR, 0.05-0.24] vs. 0.15-0.43 × 10³/µL). NK cell counts were not associated with mortality or prior COVID-19 infection.
Conclusions:
Patients with mucormycosis show decreased circulating NK cell counts, suggesting immune dysregulation. These findings describe a distinct immunologic phenotype rather than a causal or prognostic marker.
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