30 research outputs found

    Karakteristik Peredaman Getaran Konstruksi Model Jembatan untuk Pengembangan Sistem Diganosis Pola Gagal

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    In operation, the bridge structure is subjected to load variation both in the form of static load and dynamic load in variation of load intensity and frequency. In bridge structures made of steel structures, dynamic loading conditions can cause loosening of bolts, cracks and even structural failures. This paper describes the method of determining the damping bridge constant (c) by the logarithmic decrement calculation method of the vibration data generated by the impulse load. Furthermore the damping constant is used to calculate the vibration response equation of the structure along with the mass constant (m) and the stiffness of the structure (k). The mass constants are obtained by measurement whereas the stiffness constant of the structure is obtained by FEM modeling for open and closed structure models. The results of the analysis will be used to interpret the pattern of failed structures in the development of the diagnostic system. The calculation of damping constant for open and closed model is 0.07556 and 0.12513, while mass and stiffness constant for closed and open model model is 18 kg and 9 kg and 9523809.524 N / m and 183486.2 N / m for stiffness constant

    Inflammatory profile of vertically HIV-1 infected adolescents receiving ART in Cameroon: a contribution toward optimal pediatric HIV control strategies

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    Antiretroviral therapy (ART) has improved the lifespan of people living with HIV. However, their immune system remains in a state of sustained activation/inflammation, which favors viral replication and depletion of helper T-cells with varying profiles according to ART-response. We herein sought to ascertain the inflammatory profile of adolescents living with perinatal HIV-1 infection (ALPHI) receiving ART in an African context. In this cross-sectional and comparative study among ART-experienced ALPHI in Yaoundé-Cameroon, HIV-1 RNA was measured by Abbott Real-time PCR; CD4 cells were enumerated using flow cytometry; serum cytokines were measured by ELISA; HIV-1 proviral DNA was genotyped by Sanger-sequencing; and archived drug resistance mutations (ADRMs) were interpreted using Stanford HIVdb.v9.0.1. Overall, 73 adolescents were enrolled (60 ALPHI and 13 HIV-1 negative peers) aged 15 (13-18) years; 60.00% were female. ART median duration was 92 (46-123) months; median viral load was 3.99 (3.17-4.66) RNA Log10 (copies)/mL and median CD4 count was 326 (201-654) cells/mm3. As compared to HIV-negative adolescents, TNFα was highly expressed among ALPHI (p<0.01). Following a virological response, inflammatory cytokines (IFNγ and IL-12), anti-inflammatory cytokines (IL-4 and IL-10) and inflammation-related cytokines (IL-6 and IL-1β) were highly expressed with viral suppression (VS) vs. virological failure (VF), while the chemokine CCL3 was highly expressed with VF (p<0.01). Regarding the immune response, the inflammatory cytokine TNFα was highly expressed in those that are immunocompetent (CD4≥500 cell/mm3) vs. immunocompromised (CD4<500 cell/mm3), p ≤ 0.01; while chemokine CCL2 was highly expressed in the immunocompromised (p<0.05). In the presence of ADRMs, IL-4 and CCL3 were highly expressed (p=0.027 and p=0.043 respectively). Among ART-experienced ALPHI in Cameroon, the TNFα cytokine was found to be an inflammatory marker of HIV infection; IFNγ, IL-1β, IL-6, and IL-12 are potential immunological markers of VS and targeting these cytokines in addition to antiretroviral drugs may improve management. Moreover, CCL3 and CCL2 are possible predictors of VF and/or being immunocompromised and could serve as surrogates of poor ART response

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