Efficacy of cell-based immunotherapies on patients with glioma: an umbrella review of systematic reviews and meta-analysis protocol.

INTRODUCTION: Glial brain tumours are highly mortal and are noted as major neurosurgical challenges due to frequent recurrence or progression. Despite standard-of-care treatment for gliomas, the prognosis of patients with higher-grade glial tumours is still poor, and hence empowering antitumour immunity against glioma is a potential future oncological prospect. This review is designed to improve our understanding of the efficacy of cell-based immunotherapies for glioma. METHODS AND ANALYSIS: This systematic review will be performed according to the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines. A comprehensive search of main electronic databases: PubMed/MEDLINE, Scopus, ISI Web of Science EMBASE and ProQuest will be done on original articles, followed by a manual review of review articles. Only records in English and only clinical trials will be encountered for full-text review. All the appropriate studies that encountered the inclusion criteria will be screened, selected and then will undergo data extraction step by two independent authors. For meta-analyses, data heterogeneity for each parameter will be first evaluated by Cochran's Q and I2 statistics. In case of possible heterogeneity, a random-effects meta-analysis will be performed and for homogenous data, fixed-effects models will be selected for reporting the results of the proportional meta-analysis. Bias risk will be assessed through Begg's and Egger's tests and will also be visualised by Funnel plots. ETHICS AND DISSEMINATION: As this study will be a systematic review without human participants' involvement, no ethical registration is required and meta-analysis will be presented at a peer-reviewed journal. PROSPERO REGISTRATION NUMBER: CRD42022373297.

Non-invasive in situ monitoring of bone scaffold activity by speckle pattern analysis.

Scaffold-based bone tissue engineering aims to develop 3D scaffolds that mimic the extracellular matrix to regenerate bone defects and damages. In this paper, we provide a laser speckle analysis to characterize the highly porous scaffold. The experimental procedure includes in situ acquisition of speckle patterns of the bone scaffold at different times under preserved environmental conditions, and follow-up statistical post-processing toward examining its internal activity. The activity and overall viscoelastic properties of scaffolds are expressed via several statistical parameters, and the variations in the computed parameters are attributed to time-varying activity of the samples during their internal substructure migration.

Flat Wall Proximity Effect on Micro-Particle Sedimentation in Non-Newtonian Fluids.

We investigate the sedimentation of colloidal micro-spheres and red blood cells (RBCs) in non-Newtonian fluid - silicone oil with different viscosities. We use digital holographic microscopy (DHM) to obtain volumetric information of the sedimenting micro-objects. Especially, the numerical refocusing feature of DHM is used to extract the depth information of multiple particles moving inside the fluid. The effects of proximity to a flat wall and the non-Newtonian behavior on the sedimenting micro-spheres and RBCs are studied by trajectory analyzing and velocimetry. We observe that for lower viscosity values the proximity effect is more pronounced. The variation rate of the particle falling velocities versus their distance to the flat wall decreases by increasing the viscosity of the fluid. For RBCs, however, the decreasing of the velocity variations have a smoother trend. The experimental results verify the theoretical prediction that, similar to Newtonian case, a correction factor in Stokes' law suffices for describing the wall effect.

Speckle pattern analysis of crumpled papers.

In this paper, we show that laser speckle analysis (LSA) can provide valuable information about the structure of crumpled thin sheets. Crumpling and folding of slender objects are present in several phenomena and in various ranges of size, e.g., paper compaction, cortical folding in brains, DNA packing in viral capsids, and flower buds, to name a few. The analysis of laser speckles, both numerical and graphical, is a source of information about the activity of biological or non-biological materials, and the development of digital electronics, which brought the ease of image processing, has opened new perspectives for a spectrum of LSA applications. LSA is applied on randomly crumpled and one-, two-, and three-times folded papers, and appreciable differences in LSA parameters are observed. The methodology can be applied for easy-to-implement quantitative assessment of similar phenomena and samples.

Digital holographic microscopy of phase separation in multicomponent lipid membranes.

Lateral in-homogeneities in lipid compositions cause microdomains formation and change in the physical properties of biological membranes. With the presence of cholesterol and mixed species of lipids, phospholipid membranes segregate into lateral domains of liquid-ordered and liquid-disordered phases. Coupling of two-dimensional intralayer phase separations and interlayer liquid-crystalline ordering in multicomponent membranes has been previously demonstrated. By the use of digital holographic microscopy (DHMicroscopy), we quantitatively analyzed the volumetric dynamical behavior of such membranes. The specimens are lipid mixtures composed of sphingomyelin, cholesterol, and unsaturated phospholipid, 1,2-dioleoyl-sn-glycero-3-phosphocholine. DHMicroscopy in a transmission mode is an effective tool for quantitative visualization of phase objects. By deriving the associated phase changes, three-dimensional information on the morphology variation of lipid stacks at arbitrary time scales is obtained. Moreover, the thickness distribution of the object at demanded axial planes can be obtained by numerical focusing. Our results show that the volume evolution of lipid domains follows approximately the same universal growth law of previously reported area evolution. However, the thickness of the domains does not alter significantly by time; therefore, the volume evolution is mostly attributed to the changes in area dynamics. These results might be useful in the field of membrane-based functional materials.