Ashcroft v. Iqbal: The Question of a Heightened Standard of Pleading in Qualified Immunity Cases

Background We have previously shown that Lactobacillus reuteri supplementation from pregnancy week 36 and to the infant through the first year of life decreased the prevalence of IgE-associated eczema at 2 years. The underlying immunological mechanisms are unknown, however. Objective To investigate the immunomodulatory effect of probiotic supplementation on allergen- and mitogen-induced immune responses in children until 2 years of age. Methods Blood mononuclear cells were collected at birth, 6, 12 and 24 months from 61 children (29 probiotic and 32 placebo treated) and cultured with ovalbumin, birch and cat extract and Phytohaemagglutinin (PHA). Cytokine and chemokine secretion was determined using an in-house multiplexed Luminex assay and ELISA. Real-time PCR was performed to investigate the Ebi3, Foxp3, GATA-3 and T-bet mRNA expression. Results Probiotic treatment was associated with low cat-induced Th2-like responses at 6 months (IL-5, P = 0.01, and IL-13, P = 0.009), with a similar trend for IL-5 at 12 months (P = 0.09). Cat-induced IFN-γ responses were also lower after probiotic than after placebo treatment at 24 months (P = 0.007), with similar findings for the anti-inflammatory IL-10 at birth (P = 0.001) and at 12 months (P = 0.009). At 24 months, Th2-associated CCL22 levels were lower in the probiotic than in the placebo group after birch stimulation (P = 0.02), with a similar trend after ovalbumin stimulation (P = 0.07). Lower CCL22 levels were recorded at 12 and 24 months (P = 0.03 and P = 0.01) after PHA stimulation. Conclusion and Clinical Relevance Lactobacillus reuteri supplementation decreases allergen responsiveness and may enhance immunoregulatory capacity during infancy. L. reuteri supplementation from week 36 and during the first year of life significantly decreases IgE-associated eczema and lowers allergen and mitogen responsiveness.Funding Agencies|Swedish Research Council|K2011-56X-21854-01-06|Ekhaga Foundation||Olle Engkvist Foundation||Heart and Lung foundation||Research Council for the South-East Sweden|F2000-106|Swedish Asthma and Allergy Association||Cancer and Allergy Association||BioGaia AB, Stockholm, Sweden||University Hospital of Linkoping, Sweden||</p

Strategic choice of measures: A Swedish method for deciding on infrastructure investments

Since 2013 the study of strategic choice of measures has been a part of the process for the strategic and economic planning of the transport system in Sweden. The main objective in implementing a new planning process for infrastructure was to ensure safe and cost-efficient solutions which contribute to sustainable development and the fulfilment of the Swedish transport policy. The method for strategic choice of measures is focused on facilitating collaboration between the actors that have a responsibility in planning the transport system as well as enabling involvement of the general public and other actors. The methodology is divided into four phases. Initiate - Making the decision of starting a study, involving the closest concerned actors and deciding on the main aim of the study as well as the cost and time frame.Understand the situation - Defining the problems needs and deficiencies, setting a scope for the study, describing the current situation and the ‘zero option’ and agreeing on which goals the measures should reach. Test possible solutions - Identify possible measures with the help of the ‘four-step principle’ and within all modes of transport and assess the measures to see if they contribute to the goal of the study, is economically sound, does not lead to any negative consequences etc.Form a direction and recommend measures - Recommend measures or a combination of measures and hopefully reach an agreement between the actors. There are some adjustments to be made to the method, but there seems to be a consensus that the method for strategic choice of measures has led to a better understanding of the different actors’ points of views - both the problems and needs within the transport system but also the issues and limitations within their respective organisations. This is something that could benefit the Danish authorities, especially since they have separate authorities for road and railway

Long-lived charge separation in dye-semiconductor assemblies: A pathway to multi-electron transfer reactions

Solar energy has the potential of providing the world with clean and storable energy. In principle, solar fuels can be generated by light absorption followed by primary charge separation and secondary charge separation to reaction centres. However this comes with several challenges, including the need for long-lived charge separation and accumulation of several charges. This Feature Article focuses on how to achieve long-lived charge separation in dye sensitized semiconductor assemblies and the way towards multi-electron transfer through conduction band mediation, aiming at solar fuel generation. Herein, we discuss various examples of how the charge separated lifetime can be extended and potential ways of achieving one or multiple electron transfer in these assemblies

Jag valde livet! : En studie av alkoholisters olika vägar ut ur alkoholmissbruk

The purpose of this essay was to find out what alcoholics themselves mean were the way out of their drinking abuse. The questions at stake are: · What kind of context did the interviewed live in before and after the turning point? · How did the process of getting out of the alcohol abuse look like? · What different factors may have influenced the turning point, the maintenance and the interviewee's choice to stop the abuse of alcohol? · Where there any other important occurrences that may have had an impact on their decision to stop drinking? For the investigation we have interviewed three women and five men. They all have had sever problems with alcohol, but all of them also have found a way out of the abuse. Our research shows that the way out of alcohol abuse is very complex and individual. The turning point is rather a process than a single occurrence. Our research also shows that the interaction between the alcohol and important individuals in their immediate surroundings are the absolute most important factor to stop using alcohol in a destructive way but also important when it comes to maintaining soberness

Optically Switchable NIR Photoluminescence of PbS Semiconducting Nanocrystals using Diarylethene Photoswitches

Precisely modulated photoluminescence (PL) with external control is highly demanded in material and biological sciences. However, it is challenging to switch the PL on and off in the NIR region with a high modulation contrast. Here, we demonstrate that reversible on and off switching of the PL in the NIR region can be achieved in a bicomponent system comprised of PbS semiconducting nanocrystals (NCs) and diarylethene (DAE) photoswitches. Photoisomerization of DAE to the ring-closed form upon UV light irradiation causes substantial quenching of the NIR PL of PbS NCs due to efficient triplet energy transfer. The NIR PL fully recovers to an on state upon reversing the photoisomerization of DAE to the ring-open form with green light irradiation. Importantly, fully reversible switching occurs without obvious fatigue, and the high PL on/off ratio (&gt;100) outperforms all previously reported assemblies of NCs and photoswitches

Photophysical characterization of the 9,10-disubstituted anthracene chromophore and its applications in triplet-triplet annihilation photon upconversion

Molecules based on anthracene are commonly used in applications such as OLEDs and triplet-triplet annihilation upconversion. In future design of blue emitting materials it is useful to know which part of the molecule can be altered in order to obtain new physical properties without losing the inherent optical properties. We have studied the effect of substitution of 9,10-substituted anthracenes. Eight anthracenes with aromatic phenyl and thiophene substituents were synthesised, containing both electron donating and accepting groups. The substitutions were found to affect the UV/Vis absorption only to a small extent, however the fluorescence properties were more affected with the thiophene substituents that decreased the fluorescence quantum yield from unity to <10%. DFT calculations confirm the minor change in absorption and indicate that the first and second triplet state energies are also unaffected. Finally the three most fluorescent derivatives 4-(10-phenylanthracene-9-yl) pyridine, 9-phenyl-10-(4-(trifluoromethyl)phenyl) anthracene and 4-(10-phenylanthracene-9-yl) benzonitrile were successfully utilized as annihilators in a triplet-triplet annihilation upconversion (TTA-UC) system employing platinum octaethylporphyrin as the sensitizer. The observed upconversion quantum yields, phi(UC), slightly exceeded that of the benchmark annihilator 9,10-diphenylanthracene (DPA)

Two-colour photoswitching in photoresponsive inorganic thin films

Herein we report the first example of an inorganic photochromic material that allows for spatial addressability. We designed a photoresponsive thin film based on a ruthenium sulfoxide complex, [Ru(deeb)2PySO-iPr]2+, which was immobilized onto a mesoporous ZrO2 surface. The resulting material allows for all-optical detection and shows reversible, selective, photochromic behavior that can be cycled back and forth. The photosiomerization quantum yield is lower on the film than in solution which is attributed to a combination of the immobilization and steric hindrance by molecules in close proximity as evident from a surface coverage dependence of the photoisomerization quantum yield. The results reported here provide an important step towards inorganic photoswitchable materials

Selective Photocatalytic Reduction of CO2-to-CO in Water using a Polymeric Carbon Nitride Quantum Dot/Fe-Porphyrin Hybrid Assembly

Visible light-driven conversion of CO2 into more value-added products is a promising technology not only for diminution of CO2 emission but also for solar energy storage in the form of chemical energy. However, photocatalytic materials that can efficiently and selectively reduce CO2-to-CO in a fully aqueous solution typically involve precious metals that limit their suitability for large scale applications. Herein, a novel photocatalytic assembly is reported, consisting of polymeric carbon nitride quantum dots (CNQDs) as the visible light absorber and a Fe-porphyrin complex (Fe-p-TMA) as the catalyst for CO2-to-CO conversion. Both components were carefully selected to allow for excellent solubility in water as well as improved electronic communication through complementary electrostatic and π-π interactions. This CNQD ⋅ [Fe-p-TMA] hybrid assembly, at the optimized molar ratio, can produce CO with a turnover number (TON) exceeding 105 and selectivity ∼96 % after 10 hours of visible light irradiation (400–700 nm). It is postulated that the enhanced CO2-to-CO transformation performance is due to the convenience of a more direct charge transfer (CT) pathway between the CNQDs and [Fe-p-TMA] motif

Excited State Dynamics of Bistridentate and Trisbidentate RuII Complexes of Quinoline-Pyrazole Ligands

Three homoleptic ruthenium(II) complexes, [Ru(Q3PzH)3]2+, [Ru(Q1Pz)3]2+, and [Ru(DQPz)2]2+, based on the quinoline-pyrazole ligands, Q3PzH (8-(3-pyrazole)-quinoline), Q1Pz (8-(1-pyrazole)-quinoline), and DQPz (bis(quinolinyl)-1,3-pyrazole), have been spectroscopically and theoretically investigated. Spectral component analysis, transient absorption spectroscopy, density functional theory calculations, and ligand exchange reactions with different chlorination agents reveal that the excited state dynamics for Ru(II) complexes with these biheteroaromatic ligands differ significantly from that of traditional polypyridyl complexes. Despite the high energy and low reorganization energy of the excited state, nonradiative decay dominates even at liquid nitrogen temperatures, where triplet metal-to-ligand-charge-transfer emission quantum yields range from 0.7 to 3.8%, and microsecond excited state lifetimes are observed. In contrast to traditional polypyridyl complexes where ligand exchange is facilitated by expansion of the metal-ligand bonds to stabilize a metal-centered state, photoinduced ligand exchange occurs in the bidentate complexes despite no substantial MC state population, while the tridentate complex is extremely photostable despite an activated decay route, highlighting the versatile photochemistry of nonpolypyridine ligands.\ua0\ua9 2019 American Chemical Society