Methodology Based on Vector and Scalar Measurement of Traffic Channel Power Levels to Assess Maximum Exposure to Electromagnetic Radiation Generated by 5G NR Systems

Maximum-Power Extrapolation (MPE) for mobile telecommunication sources follows an established paradigm based on the identification and measurement of a channel that acts as a power reference. Prior to the 5G era, the role of reference channel has been played by always-on broadcast signals since they had the great advantage of being always transmitted at the maximum power level allowed for a generic signal channel. However, the beamforming implemented by 5G sources obliges us to rethink this approach. In fact, with beamforming the 5G source can transmit data traffic streams through a beam characterized by a much higher gain than the broadcast one. This implies that the detected power for traffic beams could be much higher than the corresponding power of broadcast beams. In this paper, a novel approach for 5G MPE procedure is presented, where the direct measurement of the received power of a traffic beam is used to assess the maximum exposure generated by a 5G system. An innovative specific experimental setup is also proposed, with the use of a User Equipment (UE) with the aim of forcing the traffic beam toward the measurement positions. In this way, it is possible to directly measure the power of each Resource Element (RE) transmitted by the traffic beam. As opposed to other MPE proposals for 5G, the discussed technique does not require any correction of the measured data since it relies only on the traffic beam pointing toward the measurement position, simplifying the overall MPE procedure and thus reducing the uncertainty of the MPE estimated field strength

New Microbicidal Functions of Tracheal Glands: Defective Anti-Infectious Response to Pseudomonas aeruginosa in Cystic Fibrosis

Tracheal glands (TG) may play a specific role in the pathogenesis of cystic fibrosis (CF), a disease due to mutations in the cftr gene and characterized by airway inflammation and Pseudomonas aeruginosa infection. We compared the gene expression of wild-type TG cells and TG cells with the cftr ΔF508 mutation (CF-TG cells) using microarrays covering the whole human genome. In the absence of infection, CF-TG cells constitutively exhibited an inflammatory signature, including genes that encode molecules such as IL-1α, IL-β, IL-32, TNFSF14, LIF, CXCL1 and PLAU. In response to P. aeruginosa, genes associated with IFN-γ response to infection (CXCL10, IL-24, IFNγR2) and other mediators of anti-infectious responses (CSF2, MMP1, MMP3, TLR2, S100 calcium-binding proteins A) were markedly up-regulated in wild-type TG cells. This microbicidal signature was silent in CF-TG cells. The deficiency of genes associated with IFN-γ response was accompanied by the defective membrane expression of IFNγR2 and altered response of CF-TG cells to exogenous IFN-γ. In addition, CF-TG cells were unable to secrete CXCL10, IL-24 and S100A8/S100A9 in response to P. aeruginosa. The differences between wild-type TG and CF-TG cells were due to the cftr mutation since gene expression was similar in wild-type TG cells and CF-TG cells transfected with a plasmid containing a functional cftr gene. Finally, we reported an altered sphingolipid metabolism in CF-TG cells, which may account for their inflammatory signature. This first comprehensive analysis of gene expression in TG cells proposes a protective role of wild-type TG against airborne pathogens and reveals an original program in which anti-infectious response was deficient in TG cells with a cftr mutation. This defective response may explain why host response does not contribute to protection against P. aeruginosa in CF

Calculation of atomic spontaneous emission rate in 1D finite photonic crystal with defects

We derive the expression for spontaneous emission rate in finite one-dimensional photonic crystal with arbitrary defects using the effective resonator model to describe electromagnetic field distributions in the structure. We obtain explicit formulas for contributions of different types of modes, i.e. radiation, substrate and guided modes. Formal calculations are illustrated with a few numerical examples, which demonstrate that the application of effective resonator model simplifies interpretation of results.Comment: Cent. Eur. J. Phys, in pres

Coxiella burnetii, the Agent of Q Fever, Replicates within Trophoblasts and Induces a Unique Transcriptional Response

Q fever is a zoonosis caused by Coxiella burnetii, an obligate intracellular bacterium typically found in myeloid cells. The infection is a source of severe obstetrical complications in humans and cattle and can undergo chronic evolution in a minority of pregnant women. Because C. burnetii is found in the placentas of aborted fetuses, we investigated the possibility that it could infect trophoblasts. Here, we show that C. burnetii infected and replicated in BeWo trophoblasts within phagolysosomes. Using pangenomic microarrays, we found that C. burnetii induced a specific transcriptomic program. This program was associated with the modulation of inflammatory responses that were shared with inflammatory agonists, such as TNF, and more specific responses involving genes related to pregnancy development, including EGR-1 and NDGR1. In addition, C. burnetii stimulated gene networks organized around the IL-6 and IL-13 pathways, which both modulate STAT3. Taken together, these results revealed that trophoblasts represent a protective niche for C. burnetii. The activation program induced by C. burnetii in trophoblasts may allow bacterial replication but seems unable to interfere with the development of normal pregnancy. Such pathophysiologocal processes should require the activation of immune placental cells associated with trophoblasts

Orientia tsutsugamushi Stimulates an Original Gene Expression Program in Monocytes: Relationship with Gene Expression in Patients with Scrub Typhus

Orientia tsutsugamushi is the causal agent of scrub typhus, a public health problem in the Asia-Pacific region and a life-threatening disease. O. tsutsugamushi is an obligate intracellular bacterium that mainly infects endothelial cells. We demonstrated here that O. tsutsugamushi also replicated in monocytes isolated from healthy donors. In addition, O. tsutsugamushi altered the expression of more than 4,500 genes, as demonstrated by microarray analysis. The expression of type I interferon, interferon-stimulated genes and genes associated with the M1 polarization of macrophages was significantly upregulated. O. tsutsugamushi also induced the expression of apoptosis-related genes and promoted cell death in a small percentage of monocytes. Live organisms were indispensable to the type I interferon response and apoptosis and enhanced the expression of M1-associated cytokines. These data were related to the transcriptional changes detected in mononuclear cells isolated from patients with scrub typhus. Here, the microarray analyses revealed the upregulation of 613 genes, which included interferon-related genes, and some features of M1 polarization were observed in these patients, similar to what was observed in O. tsutsugamushi-stimulated monocytes in vitro. This is the first report demonstrating that monocytes are clearly polarized in vitro and ex vivo following exposure to O. tsutsugamushi. These results would improve our understanding of the pathogenesis of scrub typhus, during which interferon-mediated activation of monocytes and their subsequent polarization into an M1 phenotype appear critical. This study may give us a clue of new tools for the diagnosis of patients with scrub typhus

Analysis of surface relief diffraction gratings made of anisotropic materials

A modal method for the analysis of surface relief gratings made with anisotropic material is presented. The structure is decomposed into a series of cascaded discontinuities between planar waveguides with stratified anisotropic dielectric. The basic problem is formulated by an integral equation which is solved numerically by the method of moments. The mode functions of the periodic region are assumed as basis functions to represent the unknown field on the junctions. Each junction is viewed as a waveguide junction problem and has been characterized by the generalized scattering matrix (GSM). The diffraction efficiencies of the grating are determined by combining the various GSM. In this way, the analysis method is stable and can be applied also to deep gratings

Analysis of surface relief diffraction gratings made of anisotropic material

A modal method for the analysis of surface relief gratings made with anisotropic material is presented. The structure is decomposed into a series of cascaded discontinuities between planar waveguides with stratified anisotropic dielectric. The basic problem is formulated by an integral equation which is solved numerically by the method of moments. The mode functions of the periodic region are assumed as basis functions to represent the unknown field on the junctions. Each junction is viewed as a waveguide junction problem and has been characterized by the generalized scattering matrix (GSM). The diffraction efficiencies of the grating are determined by combining the various GSM. In this way, the analysis method is stable and can be applied also to deep gratings