Desigualdades socioeconomicas e demograficas como fatores de risco para a artrite autorreferida: estudo de base populacional em adultos no Sul do Brasil

Abstract published in English and Portuguese English title: Socioeconomic and demographic inequalities as risk factors for self-reported arthritis: a population-based study in southern BrazilThe study aimed to estimate prevalence of self-reported arthritis or rheumatism and associated factors. This was a cross-sectional population-based study in Florianopolis, Santa Catarina State, Brazil, with 1,720 adults ranging from 20 to 59 years of age. Presence of self-reported arthritis or rheumatism was analyzed with a hierarchical approach, considering demographic, socioeconomic, and behavioral variables and use of health services. Logistic regression was used to evaluate the association between the outcome and independent variables. Prevalence of self-reported arthritis or rheumatism was 7.7% (95%CI: 6.4-8.9). The odds of self-reported arthritis were twice as high in women, and increased self-reported arthritis was directly associated with BMI > 30kg/m2 and increasing age and inversely proportional to schooling. Self-reported arthritis or rheumatism was higher in this sample than in Brazilian adults in general in 2008. The results suggest the need to plan public health policies to address this problem. = Estimar a prevalência de artrite ou reumatismo autorreferido e os fatores associados. Realizou-se um estudo transversal de base populacional em Florianópolis, Santa Catarina, Brasil, com 1.720 adultos entre 20 e 59 anos. A presença de artrite ou reumatismo autorreferido foi analisada por meio do modelo hierárquico de determinação no nível demográfico, socioeconômico, comportamental e uso de serviços de saúde. Utilizou-se análise de regressão logística para avaliar a associação entre as variáveis. A prevalência de artrite ou reumatismo autorreferido foi de 7,7% (IC95%: 6,4-8,9). A chance de artrite ou reumatismo autorreferido foi duas vezes maior entre as mulheres, maior entre aqueles com índice de massa corporal (IMC) > 30kg/m2,diretamente proporcional à idade e inversamente proporcional à escolaridade. A prevalência de artrite ou reumatismo autorreferido foi maior do que a estimativa nacional no ano de 2008. Essa realidade sugere a necessidade de um planejamento de políticas públicas voltado para esse agravo de saúde.Rafael Santos Gomes, Karen Glazer Pere

Skewed maturation of memory HIV-specific CD8 T lymphocytes

Understanding the lineage differentiation of memory T cells is a central question in immunology. We investigated this issue by analysing the expression of the chemokine receptor CCR7, which defines distinct subsets of naive and memory T lymphocytes with different homing and effector capacities and antiviral immune responses to HIV and cytomegalovirus. Ex vivo analysis of the expression of CD45RA and CCR7 antigens, together with in vitro analysis of the cell-division capacity of different memory CD8+ T-cell populations, identified four subsets of HIV- and CMV-specific CD8+ T lymphocytes, and indicated the following lineage differentiation pattern: CD45RA+ CCR7+ --> CD45RA- CCR7+ --> CD45RA- CCR7- --> CD45RA+ CCR7-. Here we demonstrate through analysis of cell division (predominantly restricted to the CCR7+ CD8+ T-cell subsets) that the differentiation of antigen-specific CD8+ T cells is a two-step process characterized initially by a phase of proliferation largely restricted to the CCR7+ CD8+ cell subsets, followed by a phase of functional maturation encompassing the CCR7- CD8+ cell subsets. The distribution of these populations in HIV- and CMV-specific CD8+ T cells showed that the HIV-specific cell pool was predominantly (70%) composed of pre-terminally differentiated CD45RA- CCR7- cells, whereas the CMV-specific cell pool consisted mainly (50%) of the terminally differentiated CD45RA+ CCR7- cells. These results demonstrate a skewed maturation of HIV-specific memory CD8+ T cells during HIV infection

Genetically Encoded Fluorescent Biosensors to Explore AMPK Signaling and Energy Metabolism

International audienceMaintenance of energy homeostasis is a basic requirement for cell survival. Different mechanisms have evolved to cope with spatial and temporal mismatch between energy-providing and -consuming processes. Among these, signaling by AMP-activated protein kinase (AMPK) is one of the key players, regulated by and itself regulating cellular adenylate levels. Further understanding its complex cellular function requires deeper insight into its activation patterns in space and time at a single cell level. This may become possible with an increasing number of genetically encoded fluorescent biosensors, mostly based on fluorescence resonance energy transfer, which have been engineered to monitor metabolic parameters and kinase activities. Here, we review basic principles of biosensor design and function and the advantages and limitations of their use and provide an overview on existing FRET biosensors to monitor AMPK activation, ATP concentration, and ATP/ADP ratios, together with other key metabolites and parameters of energy metabolism