Testing intermediate-age stellar evolution models with VLT photometry of LMC clusters. I. The data

This is the first of a series of three papers devoted to the calibration of a few parameters of crucial importance in the modeling of the evolution of intermediate-mass stars, with special attention to the amount of convective core overshoot. To this end we acquired deep V and R photometry for three globular clusters of the Large Magellanic Cloud (LMC), namely NGC 2173, SL 556 and NGC 2155, in the age interval 1-3 Gyr. In this first paper, we describe the aim of the project, the VLT observations and data reduction, and we make preliminary comparisons of the color-magnitude diagrams with both Padova and Yonsei-Yale isochrones. Two following papers in this series present the results of a detailed analysis of these data, independently carried out by members of the Yale and Padova stellar evolution groups. This allows us to compare both sets of models and discuss their main differences, as well as the systematic effects that they would have to the determination of the ages and metallicities of intermediate-age single stellar populations.Comment: 27 pages with 10 figures. Accepted by the Astronomical Journa

Healthy preterm newborns: Altered innate immunity and impaired monocyte function

: Birth prior to 37 completed weeks of gestation is referred to as preterm (PT). Premature newborns are at increased risk of developing infections as neonatal immunity is a developing structure. Monocytes, which are key players after birth, activate inflammasomes. Investigations into the identification of innate immune profiles in premature compared to full-term infants are limited. Our research includes the investigation of monocytes and NK cells, gene expression, and plasma cytokine levels to investigate any potential differences among a cohort of 68 healthy PT and full-term infants. According to high-dimensional flow cytometry, PT infants have higher proportions of CD56+/- CD16+ NK cells and immature monocytes, and lower proportions of classical monocytes. Gene expression revealed lower proportions of inflammasome activation after in vitro monocyte stimulation and the quantification of plasma cytokine levels expressed higher concentrations of alarmin S100A8. Our findings suggest that PT newborns have altered innate immunity and monocyte functional impairment, and pro-inflammatory plasmatic profile. This may explain PT infants' increased susceptibility to infectious disease and should pave the way for novel therapeutic strategies and clinical interventions

Differential effects of antiretrovirals on microbial translocation and gut microbiota composition of HIV-infected patients

Introduction: Increased bacterial translocation and alterations to gut microbiota composition have been described in HIV infection and contribute to immune activation and inflammation. These effects persist despite combined antiretroviral therapy (cART). However, the contribution of different cART combinations has not yet been investigated. The aim of this study was to analyse the long-term effects of different combinations of cART on bacterial translocation and gut microbiota composition in HIV-infected patients. Methods: We carried out a cross-sectional study of 45 HIV-infected patients on cART, classified as nucleoside reverse transcriptase inhibitors (NRTIs)+ protease inhibitors (PIs) (n = 15), NRTIs+ non-nucleoside reverse transcriptase inhibitors (NNRTIs) (n = 22), and NRTIs+ integrase strand transfer inhibitors (INSTIs) (n = 8). Untreated HIV-infected patients (n = 5) and non-infected volunteers (n = 21) were also included. Soluble markers of bacterial translocation and inflammation were measured and gut microbiota composition was analysed using 16S rDNA pyrosequencing (Illumina MiSeq). Results: The NRTIs+INSTIs regimen was associated with levels of systemic inflammation that were similar to uninfected controls. The reduction in faecal bacterial diversity induced by HIV infection was also restored by this regimen. HIV infection was more closely related to changes in lower taxonomic units and diversity rather than at the phylum level. The NRTIs+PIs regimen showed the highest reduction in bacterial species, whereas NRTIs+INSTIs induced a minor loss of bacterial species and a significant increase in others. Conclusions: Our study demonstrated that INSTI-based ART was associated with levels of systemic inflammation and microbial diversity similar to that of uninfected controls. The role of INSTIs other than raltegravir needs to be further investigated. Patients on the NRTIs+PIs regimen presented the highest reduction in bacterial species compared with other antiretrovirals and naive patients. Thus, different cART regimens are associated with diverse profiles in gut microbiota composition. Longitudinal and functional studies are needed to better understand these findings

A data base for Galaxy evolution modeling

This paper represents a collective effort to provide an extensive electronic database useful for the interpretation of galaxy properties