On-site monitoring for better selection of stone repairs: a case study

Weathering of clay-bearing sandstones does not only depend on material properties but also on the environmental conditions they are exposed to. The same is true for repaired stones, in which the compatibility of the repair mortar should be studied not only in terms of material properties, but also in terms of the climatic conditions it will be sub- jected, in order to maximize this compatibility. This paper proposes a methodology to quantify the thermal and hygric stresses in clay-bearing sandstones and their repair, based on the measurement of temperature and relative humidity at the surface and at several depths in a repaired and a non-repaired stone, as well as wind-driven rain and absorbed water. This is illustrated by a case study in an historical building. The data are used to quantify the stresses in the mate- rials and to propose possible degradation mechanisms.ISSN:2050-744

Effect of Recombinant alpha1-Antitrypsin Fc-Fused (AAT-Fc)Protein on the Inhibition of Inflammatory Cytokine Production and Streptozotocin-Induced Diabetes

Contains fulltext : 118341.pdf (publisher's version ) (Open Access)alpha1-Antitrypsin (AAT) is a member of the serine proteinase inhibitor family that impedes the enzymatic activity of serine proteinases, including human neutrophil elastase, cathepsin G and neutrophil proteinase 3. Here, we expressed recombinant AAT by fusing the intact AAT gene to the constant region of IgG1 to generate soluble recombinant AAT-Fc protein. The recombinant AAT-Fc protein was produced in Chinese hamster ovary (CHO) cells and purified using mini-protein A affinity chromatography. Recombinant AAT-Fc protein was tested for antiinflammatory function and AAT-Fc sufficiently suppressed tumor necrosis factor (TNF)-alpha-induced interleukin (IL)-6 in human peripheral blood mononuclear cells (PBMCs) and inhibited cytokine-induced TNFalpha by different cytokines in mouse macrophage Raw 264.7 cells. However, AAT-Fc failed to suppress lipopolysaccharide-induced cytokine production in both PBMCs and macrophages. In addition, our data showed that AAT-Fc blocks the development of hyperglycemia in a streptozotocin-induced mouse model of diabetes. Interestingly, we also found that plasma-derived AAT specifically inhibited the enzymatic activity of elastase but that AAT-Fc had no inhibitory effect on elastase activity