The authors verify whether in silicosis the accumulation of silicon dioxide (SiO2) particles in the lung can induce changes of the activated T lymphocytes in the peripheral blood. The lymphoblastic transformation of lymphocytes stimulated with phytohemagglutinin (PHA), concanavalin A (Con A), Mycobacterium tuberculosis (Mt) and purified protein derivative (PPD) was studied using the classical methods. It was observed that in patients exposed to SiO2 lymphocyte reactivity to the above stimulants decreases. Significant differences between patients and controls were observed only in the response to PHA (p < 0.001).

Humans↗

PubMedDate not supplied

Considerations on the changes of certain immunologic cells in silicosis.

Cell-mediated immunity was estimated in a group of 68 patients divided into three subgroups according to the evolutive stage of disease. It was demonstrated that in silicosis there is a disturbance of immunity. The detection of E rosettes and of activated rosettes was carried out according to the classical method. The mean percentage of total T lymphocytes was found lower in silicosis (62 +/- 2% statistically significant for p < 0.05), compared to the control group (66 +/- 4.6%). The study revealed a decrease of T helper lymphocytes, an increase of T suppressor/cytotoxic lymphocytes and a decrease of the T helper/T suppressor ratio (1.96 +/- 0.13) in silicosis as compared to the control group (2.83 +/- 0.31). The presence of these changes in silicotic patients suggested the participation of cell-mediated immunity in the pathogenesis of disease, the cell mediated immunity being directly responsible for the evolution of silicosis.

Adult↗

PubMedDate not supplied

Silicosis related changes in serum copper.

To ascertain the diagnostic and prognostic value of serum copper in silicosis, this trace element was determined in 68 patients (all males), aged varied between 20 and 60 years (mean age 44 +/- 2.3 years). The same determination was carried out in a control group of 35 healthy subjects. The patients were distributed into three subgroups according to the evolutive stage of disease. The mean value of serum copper increased gradually from stage to stage reaching in stage III the highest copper mean value (p < 0.01). Serum copper concentrations also increased with the severity of the disease. These changes suggest that copper is directly responsible for the lung changes in silicosis and can be used as an indicator of the severity of the inflammatory reaction.

Adult↗

PubMedDate not supplied

[Medicamentous films].

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Adhesives↗

PubMedDate not supplied

[Stomatologic changes following tetracycline therapy].

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Child↗

PubMedDate not supplied

The role of certain immunologic parameters in silicosis.

The paper presents some possibilities of estimating the immunologic aggression in silicosis in a group of 68 patients divided into three subgroups according to the evolutive stage of disease. The results were compared with the data obtained in a control group of 35 clinically healthy subjects not subjected to respiratory noxae. Parameters such as the immunogram (IgG, IgA IgM, IgD), the C3 complement, the circulating immune complexes (CIC) and the C reactive protein (CRP) were investigated using classical immunochemical methods. It was observed that the immunoglobulin titer presented a polyclonal increase. The mean values of C3 complement decreased in stages I and II of disease. The CIC level presented high mean values unrelated to the stage of the disease. The incidence of CRP was found high in stage III. It was demonstrated that there is no significant correlation between the humoral immunologic abnormalities and the radiologic changes or the depression of the pulmonary functional test. These changes suggest that the humoral immunologic abnormalities are not directly responsible for the lung changes in silicosis and cannot be used as a predictive indicator of the severity of the disease or of its progress. The data obtained showed a hyperreactivity of the humoral mediated immunity over the whole course of the disease thus supporting the assumption of an immunopathogenic mechanism in this disease.

Adult↗