Chemokines involved in the early inflammatory response and in pro-tumoral activity in asbestos-exposed workers from an Italian coastal area with territorial clusters of pleural malignant mesothelioma
Objectives: Immune mediators are likely to be relevant for the biological response to asbestos exposure.
The aim of this study was to investigate the association between immune mediators involved in inflammation,
cell survival and angiogenesis, and asbestos-related diseases in workers from a coastal area of
North-East Italy with a high incidence of pleural malignant mesothelioma (PMM).
Materials and methods: A selected custom set of 12 soluble mediators was evaluated with a Luminex
platform in sera, pleural fluid and mesothelioma biopsies from 123 asbestos-exposed workers (38 free
from pleural-pulmonary disorders, 46 with non-malignant asbestos diseases, 39 with PMM) and in sera
from 33 healthy controls from the same territorial area.
Results: Increased immune mediator concentrations were observed in the sera of the asbestos-exposed
workers compared to controls for human fibroblast growth factor (FGF-b), vascular endothelial growth
factor (VEGF), CCL5 (RANTES), CXCL10 (IP-10), CLEC11A (SCGF-b), CCL27 (CTACK), CCL11 (EOTAXIN), IL-5
and IL-6 (p < 0.001). The chemokines IP-10 and RANTES were associated with the severity of asbestosrelated
diseases. In the workers with PMM, the immune proteins secreted by mesothelioma biopsies
showed detectable levels of RANTES, VEGF, and IP-10. In the same workers with PMM, a significant
relationship between serum and pleural fluid concentrations was found for RANTES alone.
Conclusions: Occupational exposure to asbestos seems to drive the production of specific growth factors
dually involved in the early inflammatory response and in pro-tumoral activity before clinical evidence
of related disorders, suggesting that their over-expression may precede the onset of asbestos-related
diseases. These findings suggest that some chemokines may have a prognostic role in the progression
of asbestos-related diseases and could be used for the health surveillance of either workers with
an occupational history of asbestos exposure or patients affected by non-malignant asbestos-related
diseases.