5 research outputs found

    Coinfection of Tuberculosis Pneumonia and COVID-19 in a Patient Vaccinated with Bacille Calmette-Guérin (BCG). Case Report

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    COVID-19 is a respiratory tract infection caused by the new coronavirus SARS-COV2 that can be complicated by acute distress respiratory syndrome and multiorgan failure. In light of the high rate of mortality associated with COVID-19, pharmacological and non-pharmacological strategies to prevent the infection are currently being tested. Among non-pharmacological preventive measures, vaccines represent one of the main resources for public health. It has been suggested that Bacille Calmette-Guérin (BCG) vaccine may protect individuals against infection from COVID-19 virus, and two clinical trials addressing this question are underway. Here, we report the case of a 32-year-old woman, vaccinated with BCG when she was 1 year old, who was diagnosed with apical tuberculous pneumonia of the right lung along with COVID 19 pneumonia

    A direct methodology for the calibration of ductile damage models from a simple multiaxial test

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    In the present work a straightforward calibration procedure of ductile damage models is proposed. The direct methodology involves the use of a simple multiaxial specimen, to be tested with a universal testing machine, capable to reproduce different stress states in the material. The specimen geometry was the one proposed by Driemeier et al. [1]. In addition, a numerical-analytical procedure was devised for the identification of material strains to fracture and corresponding stress states, directly from experimental tests. This allowed to overcome the use of Finite Element Analysis and inverse methods usually adopted to retrieve the local parameters representative of the material ductility

    Additive manufacturing structural redesign of hip prostheses for stress-shielding reduction and improved functionality and safety

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    Nowadays, the total hip arthroplasty (THA) is a widespread surgical procedure, representing the best option to restore hip joint mobility in patients suffering from trauma or joint diseases. One of the well-known possible drawbacks of THA is the stress-shielding phenomenon. Some years after the surgery, the femur starts to degrade because of its persistent unloaded condition induced by the high prosthesis stiffness, which carries the great part of the load normally taken by the bone. This condition is particularly invalidating in younger patients, with longer life expectation after the operation, requiring one or multiple additional operations to restore the proper prosthesis-bone firm connection. The present study tries to address this issue proposing an innovative prosthesis design, taking advantage of the shape freedom ensured by Additive Manufacturing techniques. Additionally, the structural integrity of the novel prosthesis is assessed using a ductile damage numerical approach. Different prosthesis geometries were investigated: one conventional and commercially available already, and two more innovative geometries. For each one, a bulk solution was compared to a lighter version characterized by an inner reticular structure with a body-centred cubic unit cell and by an equivalent density of about 5%, only feasible through the additive manufacturing fabrication. Extensive Finite Element numerical simulations were carried out to compare the percentage of the induced stress shielding for the different prosthesis geometries. Pros and cons of each geometry were pointed out and eventually the most promising solution in limiting the stress shielding phenomenon was chosen. At the same time, the structural integrity of the selected design was ensured, embedding a ductile damage model in the Finite Element analysis, calibrated on a SLM Ti6Al4V, the biocompatible alloy for the prosthesis fabrication. Structural safety was evaluated under four different loading conditions: walking, stumbling, the exceptional overload due to hammering insertion during surgery and the force which induced the collapse of the implant. Additionally, the safety margin was quantified through the definition of an overall safety factor under the maximum expected load

    Effects of Temperature and Strain Rate on the Ductility of an API X65 Grade Steel

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    In the last few decades, great effort has been spent on advanced material testing and the development of damage models intended to estimate the ductility and fracture of ductile metals. While most studies focused on static testing are applied at room temperatures only, in this paper, multiaxial tests have been executed to investigate the effects of dynamic action and temperature on the mechanical and fracture behavior of an API X65 steel. To this end, a Split Hopkinson Bar (SHB) facility for dynamic tests, and a uniaxial testing machine equipped with a high-temperature furnace, were used. Numerical simulations of the experiments were setup for calibration and validation purposes. Based on the experimental results, the Johnson–Cook and Zerilli–Armstrong plasticity models were first tuned, resulting in a good experimental–numerical match. Secondly, the triaxiality and Lode angle dependent damage models proposed by Bai–Wierzbicki and Coppola–Cortese were also calibrated. The comparison of the fracture surfaces predicted by the damage models under different loading conditions showed, as expected, an overall significant increase in ductility with temperature; an appreciable increase in ductility was also observed with the increase in strain rate, in the range of low and moderate triaxialities

    Immunosuppressive Therapies Differently Modulate Humoral- and T-Cell-Specific Responses to COVID-19 mRNA Vaccine in Rheumatoid Arthritis Patients

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    Objective: To assess in rheumatoid arthritis (RA) patients, treated with different immunosuppressive therapies, the induction of SARS-CoV-2-specific immune response after vaccination in terms of anti-region-binding-domain (RBD)-antibody- and T-cellspecific responses against spike, and the vaccine safety in terms of clinical impact on disease activity. Methods: Health care workers (HCWs) and RA patients, having completed the BNT162b2-mRNA vaccination in the last 2 weeks, were enrolled. Serological response was evaluated by quantifying anti-RBD antibodies, while the cell-mediated response was evaluated by a whole-blood test quantifying the interferon (IFN)-g-response to spike peptides. FACS analysis was performed to identify the cells responding to spike stimulation. RA disease activity was evaluated by clinical examination through the DAS28crp, and local and/or systemic clinical adverse events were registered. In RA patients, the ongoing therapeutic regimen was modified during the vaccination period according to the American College of Rheumatology indications. Results: We prospectively enrolled 167 HCWs and 35 RA patients. Anti-RBD-antibodies were detected in almost all patients (34/35, 97%), although the titer was significantly reduced in patients under CTLA-4-inhibitors (median: 465 BAU/mL, IQR: 103-1189, p<0.001) or IL-6-inhibitors (median: 492 BAU/mL, IQR: 161-1007, p<0.001) compared to HCWs (median: 2351 BAU/mL, IQR: 1389-3748). T-cell-specific response scored positive in most of RA patients [24/35, (69%)] with significantly lower IFN-g levels in patients under biological therapy such as IL-6-inhibitors (median: 33.2 pg/mL, IQR: 6.1-73.9, p<0.001), CTLA-4-inhibitors (median: 10.9 pg/mL, IQR: 3.7-36.7, p<0.001), and TNF-ainhibitors (median: 89.6 pg/mL, IQR: 17.8-224, p=0.002) compared to HCWs (median: 343 pg/mL, IQR: 188-756). A significant correlation between the anti-RBD-antibody titer and spike-IFN-g-specific T-cell response was found in RA patients (rho=0.432, p=0.009). IFN-g T-cell response was mediated by CD4+ and CD8+ T cells. Finally, no significant increase in disease activity was found in RA patients following vaccination. Conclusion: This study showed for the first time that antibody-specific and whole-blood spike-specific T-cell responses induced by the COVID-19 mRNA-vaccine were present in the majority of RA patients, who underwent a strategy of temporary suspension of immunosuppressive treatment during vaccine administration. However, the magnitude of specific responses was dependent on the immunosuppressive therapy administered. In RA patients, BNT162b2 vaccine was safe and disease activity remained stabl
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