Analysis of Immune Cell Subsets in Peripheral Blood from Patients with Engineered Stone Silica-Induced Lung Inflammation

• Published in: International journal of molecular sciences 2024-06, Vol.25 (11), p.5722
• Main Authors: Jiménez-Gómez, Gema, Campos-Caro, Antonio, García-Núñez, Alejandro, Gallardo-García, Alberto, Molina-Hidalgo, Antonio, León-Jiménez, Antonio
• Format: Article
• Language: English
• Subjects: Adult; Aged; artificial stone; Blood; Case-Control Studies; Cells; Cytotoxicity; Ethylenediaminetetraacetic acid; Female; Flow cytometry; human; Humans; immune cell subsets; Immune system; Inflammation; Killer Cells, Natural - immunology; Leukocytes; Lymphocyte Subsets - immunology; Lymphocyte Subsets - metabolism; Lymphocytes; Male; Medical equipment and supplies industry; Medical test kit industry; Middle Aged; Neutrophils; Patients; Pneumonia - blood; Pneumonia - immunology; Silica; Silicon Dioxide; Silicosis; Silicosis - blood; Silicosis - immunology; Silicosis - pathology; Sociodemographics
• ISSN: 1422-0067; 1661-6596; 1422-0067
• DOI: 10.3390/ijms25115722

Silicosis caused by engineered stone (ES-silicosis) is an emerging worldwide issue characterized by inflammation and fibrosis in the lungs. To our knowledge, only a few reports have investigated leukocyte/lymphocyte subsets in ES-silicosis patients. The present study was designed to explore the proportions of the main lymphocyte subsets in ES-silicosis patients stratified into two groups, one with simple silicosis (SS) and the other with a more advanced state of the disease, defined as progressive massive fibrosis (PMF). The proportions of B (memory and plasmablasts) cells, T (helper, cytotoxic, regulatory) cells, and natural killer (NK) (regulatory and cytotoxic) cells were investigated by multiparameter flow cytometry in 91 ES-silicosis patients (53 SS patients and 38 PMF patients) and 22 healthy controls (HC). Although the total number of leukocytes did not differ between the groups studied, lymphopenia was observed in patients compared to healthy controls. Compared with those in healthy controls, the proportions of memory B cells, naïve helper T cells, and the CD4 /CD8 T cells' ratio in the peripheral blood of patients with silicosis were significantly decreased, while the percentages of plasma cells, memory helper T cells, and regulatory T cells were significantly increased. For the NK cell subsets, no significant differences were found between the groups studied. These results revealed altered cellular immune processes in the peripheral blood of patients with ES-silicosis and provided further insight into silicosis pathogenesis.