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Biomedical subjects

P Prete

Publications and source records attributed to P Prete.

11 recordsLinked to original sources

Au nanoparticles prepared by physical method on Si and sapphire substrates for biosensor applications.

Gold nanoparticles heavily functionalized with oligonucleotides have been used in a variety of DNA detection methods. The optical properties of three-dimensional aggregates of Au nanoparticles in solution or deposited onto suitable surfaces have been analyzed to detect hybridization processes of specific DNA sequences as possible alternatives to fluorescent labeling methods. This paper reports on the preparation of gold nanoparticles directly deposited onto the surface of silicon (Si) and sapphire (Al2O3) substrates by a physical methodology, consisting in the thermal evaporation of a thin Au film and its successive annealing. The method guarantees the preparation of monodispersed single-crystal Au nanoparticles with a strong surface plasmon resonance (SPR) peak centered at about 540 nm. We show that the changes of SPR excitation before and after DNA functionalization and subsequent hybridization of Au nanoparticles immobilized onto Si and Al2O3 substrates can be exploited to fabricate specific biosensors devices in solid phase.

Aluminum Oxide↗

The in vitro effects of endogenous opiates on natural killer cells, antigen-specific cytolytic T cells, and T-cell subsets.

In concert with the known effects of stress on immune function, we examined a possible neurohumoral connection. The endogenous opiates beta-endorphin, dynorphin, and methionine-enkephalin were assessed for their in vitro effects on human natural killer cell activity, antigen-specific cytolysis, and numbers and ratios of T cells and T-cell subsets. Preincubation with beta-endorphin, an opiate released into the circulation during various stresses, caused a 50% reduction in natural killer cell activity. All endogenous opiates significantly decreased antigen-specific cytolysis. Inhibition of cytolysis in vitro was not mediated through an alteration of T-cell subsets or inhibition of T-cell soluble factors (interleukin 2). The direct effects of these opiates on cytolytic T-cell and natural killer cell function may provide a link between stress and disease susceptibility.

Cytotoxicity, Immunologic↗

Abrogation of the in vitro generation of the cytotoxic T-cell response to a murine tumor: the role of suppressor cells.

A reproducible in vitro assay for the effect of suppressor T cells on the generation of an in vitro cytotoxic response to a metastatic murine tumor is described. Suppression in this system is maximal. The model uses splenic T cells from DBA/2 mice bearing the MDAY-D2 metastatic tumor as suppressors of the in vitro generation of a cell mediated cytotoxic response by syngeneic tumor-bearer (i.e., primed) peripheral lymph node cells stimulated with mitomycin C-treated MDAY-D2 tumor cells. The effect of the cell mediated cytotoxic response is profound, specific and mediated by splenic T cells. The suppressor T cells appear to impair precursor rather than mature cytotoxic cells. A highly immunogenic variant of MDAY-D2, namely MDWI, does not generate a suppressor response. Suppressor T cells from an MDAY-D2 tumor-bearer cannot suppress the in vitro response to MDWI. This model of potent suppressor T-cell action is highly reproducible and offers an opportunity for the analysis of why some tumors generate an effective cell mediated cytotoxic response which others stimulate dramatic suppressor T-cell response.

Animals↗

Diagnostic errors in polymyalgia rheumatica and temporal arteritis.

Incomplete clinical response or persistence of a rapid ESR despite corticosteroid treatment of polymyalgia rheumatica or temporal arteritis should always arouse suspicion and prompt a search for other diagnoses. Lumbar spinal stenosis and Pancoast's tumor are two unusual entities that can complicate or compete for the diagnosis of polymyalgia rheumatica and temporal arteritis.

Diagnostic Errors↗