Effects of psycho-educational training and stimulant medication on visual perceptual skills in children with attention deficit hyperactivity disorder

Attention deficit hyperactivity disorder (ADHD) is treated with stimulants and psycho-educational remedial programs despite limited literature support for the latter. This study aimed to examine changes in a “Test of Visual Perceptual Skills” (TVPS) that has not been previously reported in children with ADHD enrolled in such a program

Programmable Edge-to-Cloud Virtualization for 5G Media Industry: The 5G-MEDIA Approach

To ensure high Quality of Experience (QoE) for end users, many media applications require significant quantities of computing and network resources, making their realization challenging in resource constrained environments. In this paper, we present the approach of the 5G-MEDIA project, providing an integrated programmable service platform for the development, design and operations of media applications in 5G networks, facilitating media service management across the service life cycle. The platform offers tools to service developers for efficient development, testing and continuous correction of services. One step further, it provides a service virtualization platform offering horizontal services, such as a Media Service Catalogue and accounting services, as well as optimization mechanisms to flexibly adapt service operations to dynamic conditions with efficient use of infrastructure resources. The paper outlines three use cases where the platform was tested and validated

Dual targeting of CD19 and CD22 against B-ALL using a novel high-sensitivity aCD22 CAR

CAR T cells recognizing CD19 effectively treat relapsed and refractory B-ALL and DLBCL. However, CD19 loss is a frequent cause of relapse. Simultaneously targeting a second antigen, CD22, may decrease antigen escape, but is challenging: its density is approximately 10-fold less than CD19, and its large structure may hamper immune synapse formation. The characteristics of the optimal CD22 CAR are underexplored. We generated 12 distinct CD22 antibodies and tested CARs derived from them to identify a CAR based on the novel 9A8 antibody, which was sensitive to low CD22 density and lacked tonic signaling. We found no correlation between affinity or membrane proximity of recognition epitope within Ig domains 3–6 of CD22 with CART function. The optimal strategy for CD19/CD22 CART co-targeting is undetermined. Co-administration of CD19 and CD22 CARs is costly; single CARs targeting CD19 and CD22 are challenging to construct. The co-expression of two CARs has previously been achieved using bicistronic vectors. Here, we generated a dual CART product by co-transduction with 9A8-41BBζ and CAT-41BBζ (obe-cel), the previously described CD19 CAR. CAT/9A8 CART eliminated single- and double-positive target cells in vitro and eliminated CD19- tumors in vivo. CAT/9A8 CART is being tested in a phase I clinical study (NCT02443831)

Towards Serverless NFV for 5G Media Applications

The advent of virtualization and IaaS have revolutionized the telecom industry via SDN/NFV. A new wave of cloud-native PaaS promises to further improve SDN/NFV performance, portability, and cost-efficiency. In this poster, we highlight a work in progress being done in the 5G-MEDIA project [2], which pioneers the application of the serverless paradigm to NFV in the context of media intensive applications in 5G networks. Motivational use cases include tele-immersive gaming, mobile journalism and UHD content distribution. For example, consider a next-gen e-sport, in which bouts between gamers last only a few minutes. FaaS offers a clear cost-efficiency benefit for hosting such applications. An architecture is shown in Fig. 1. It includes i) an Application/Service Development Kit (SDK) to enable access to media applications development tools; ii) a Service Virtualization Platform (SVP) to run the ETSI MANO framework, the Media Service MAPE optimization component and the VIM and WIM plugins to enable NFVIs integration; iii) different NFVIs to execute media-specific VNFs. FaaS VIM is implemented for integration of FaaS with the rest of the MANO stack. It allows mixing FaaS and "regular" VNFs within the same media forwarding graph. For reference implementation, Apache OpenWhisk [1] and Kubernetes are used. The main challenge is extending the programming model to support groups of actions communicating over a network, while retaining the simplicity of FaaS

A service platform architecture enabling programmable edge-to-cloud virtualization for the 5G Media industry

Media applications are amongst the most demanding services in terms of resources, requiring huge network capacity for high bandwidth audio-visual and other mobile sensory streams. The 5G-MEDIA project aims at innovating media-related applications by investigating how these applications and the underlying 5G network should be coupled and interwork to the benefit of both. The 5G-MEDIA approach aims at delivering an integrated programmable service platform for the development, design and operations of media applications in 5G networks by providing mechanisms to flexibly adapt service operations to dynamic conditions and react upon events (e.g. to transparently accommodate auto-scaling of resources, VNF replacement, etc.). In this paper we present the 5G-MEDIA service platform architecture, which has been specifically designed to enable the development and operation of services for the nascent 5G media industry. Our approach delivers an integrated programmable service platform for the development, design and operations of media applications in 5G networks

Moderate intensity exercise training combined with inulin-propionate ester supplementation increases whole body resting fat oxidation in overweight women

Background: Our previous work has shown that oral supplementation with inulin propionate ester (IPE) reduces intra-abdominal fat and prevents weight gain and that oral propionate intake enhances resting fat oxidation. The effects of IPE combined with exercise training on energy substrate utilisation are unknown. The aim of this study was to investigate the impact of 4-weeks IPE supplementation, in combination with a moderate intensity exercise training programme, on whole body fat oxidation and on plasma GLP-1 and PYY. Methods: Twenty overweight healthy women participated in randomised parallel study and underwent 4 weeks of supervised exercise training either with IPE (EX/IPE group) or Placebo (EX/Placebo group) supplementation. Before and after the intervention participants conducted an experimental trial, which involved collection of expired gas and blood samples in the fasted state and during 7 h of the postprandial state. Results: Within groups, the EX/IPE group significantly enhanced the amount of fat (Pre, 24.1 ± 1.2 g; Post, 35.9 ± 4.0 g, P < .05) oxidised and reduced CHO (Pre, 77.8 ± 6.0 g; Post, 57.8 ± 7.7 g, P < .05) oxidised, reduced body weight (Pre, 77.3 ± 4.2 kg; Post, 76.6 ± 4.1 kg, P < .05) and body fat mass (Pre, 37.7 ± 1.9%; Post, 36.9 ± 1.9%, P < .05). In EX/Placebo group, changes in amount of fat (Pre, 36.8 ± 3.9 g; Post, 37.0 ± 4.0 g) and CHO (Pre, 62.7 ± 6.5 g; Post, 61.5 ± 7.4 g) oxidised, body weight (Pre, 84.2 ± 4.3 kg; Post, 83.6 ± 4.3 kg) and body fat mass (Pre, 40.1 ± 1.9%; Post, 38.7 ± 1.5%) were not significant (P > .05). Comparing between groups, changes in the amount of fat oxidised were significantly (P < .05) different and a trend for difference was observed for amount of CHO oxidised (P = .06) and RER (P = .06). The interventions had no impact on fasting or postprandial plasma concentrations of GLP-1 and PYY. Conclusion: Moderate intensity exercise training programmes when combined with daily oral IPE supplementation may help overweight women to achieve increase in fat oxidation. The study was registered at clinicaltrials.gov as NCT04016350

miR-155 overexpressing monocytes resemble HLA highISG15 + synovial tissue macrophages from patients with rheumatoid arthritis and induce polyfunctional CD4+ T cell activation

MicroRNAs (miRs) are known to regulate pro-inflammatory effector functions of myeloid cells, and miR dysregulation is implicated in rheumatoid arthritis (RA), a condition characterized by inflammation and destruction of the joints. We showed previously that miR-155 is increased in myeloid cells in RA and induces pro-inflammatory activation of monocytes and macrophages; however, its role at the interface between innate and adaptive immunity was not defined. Here, RNA-sequencing revealed that overexpression of miR-155 in healthy donor monocytes conferred a specific gene profile which bears similarities to that of RA synovial fluid-derived CD14+ cells and HLAhighISG15+ synovial tissue macrophages, both of which are characterized by antigen-presenting pathways. In line with this, monocytes in which miR-155 was overexpressed, displayed increased expression of HLA-DR and both co-stimulatory and co-inhibitory molecules, and induced activation of polyfunctional T cells. Together, these data underpin the notion that miR-155-driven myeloid cell activation in the synovium contributes not only to inflammation but may also influence the adaptive immune response

Cell-specific bioorthogonal tagging of glycoproteins

Altered glycoprotein expression is an undisputed corollary of cancer development. Understanding these alterations is paramount but hampered by limitations underlying cellular model systems. For instance, the intricate interactions between tumour and host cannot be adequately recapitulated in monoculture of tumour-derived cell lines. More complex co-culture models usually rely on sorting procedures for proteome analyses and rarely capture the details of protein glycosylation. Here, we report a strategy termed Bio-Orthogonal Cell line-specific Tagging of Glycoproteins (BOCTAG). Cells are equipped by transfection with an artificial biosynthetic pathway that transforms bioorthogonally tagged sugars into the corresponding nucleotide-sugars. Only transfected cells incorporate bioorthogonal tags into glycoproteins in the presence of non-transfected cells. We employ BOCTAG as an imaging technique and to annotate cell-specific glycosylation sites in mass spectrometry-glycoproteomics. We demonstrate application in co-culture and mouse models, allowing for profiling of the glycoproteome as an important modulator of cellular function