Large field homogeneous illumination in microwave-induced thermoacoustic tomography based on a quasi-conical spiral antenna

Conventional helical and horn antennas based on frequency selective surfaces have been used to provide microwave illumination in microwave-induced thermoacoustic tomography (TAT). However, the electromagnetic waves radiated from the conventional antennas are not circularly polarized and thus impair image quality. In addition, conventional antennas can provide uniform radiations only within a relatively small area and thus limit their clinical applications (e.g., breast imaging). To address these problems, we propose a quasi-conical log-spiral antenna for homogenous illumination over a large field. We theoretically and experimentally validated this approach. Tissue-mimicking phantoms were imaged. The antenna produced not only an electric field with a circular polarization but also a homogeneous illumination area with a 10 cm diameter. Accordingly, our method has advanced TAT by improving microwave illumination

Large field homogeneous illumination in microwave-induced thermoacoustic tomography based on a quasi-conical spiral antenna

Conventional helical and horn antennas based on frequency selective surfaces have been used to provide microwave illumination in microwave-induced thermoacoustic tomography (TAT). However, the electromagnetic waves radiated from the conventional antennas are not circularly polarized and thus impair image quality. In addition, conventional antennas can provide uniform radiations only within a relatively small area and thus limit their clinical applications (e.g., breast imaging). To address these problems, we propose a quasi-conical log-spiral antenna for homogenous illumination over a large field. We theoretically and experimentally validated this approach. Tissue-mimicking phantoms were imaged. The antenna produced not only an electric field with a circular polarization but also a homogeneous illumination area with a 10 cm diameter. Accordingly, our method has advanced TAT by improving microwave illumination

T cell immunity rather than antibody mediates cross-protection against Zika virus infection conferred by a live attenuated Japanese encephalitis SA14-14-2 vaccine.

Zika virus (ZIKV) and Japanese encephalitis virus (JEV) are closely related to mosquito-borne flaviviruses. Japanese encephalitis (JE) vaccine SA14-14-2 has been in the Chinese national Expanded Program on Immunization since 2007. The recent recognition of severe disease syndromes associated with ZIKV, and the identification of ZIKV from mosquitoes in China, prompts an urgent need to investigate the potential interaction between the two. In this study, we showed that SA14-14-2 is protective against ZIKV infection in mice. JE vaccine SA14-14-2 triggered both Th1 and Th2 cross-reactive immune responses to ZIKV; however, it was cellular immunity that predominantly mediated cross-protection against ZIKV infection. Passive transfer of immune sera did not result in significant cross-protection but did mediate antibody-dependent enhancement in vitro, though this did not have an adverse impact on survival. This study suggests that the SA14-14-2 vaccine can protect against ZIKV through a cross-reactive T cell response. This is vital information in terms of ZIKV prevention or precaution in those ZIKV-affected regions where JEV circulates or SA14-14-2 is in widespread use, and opens a promising avenue to develop a novel bivalent vaccine against both ZIKV and JEV. KEY POINTS: • JEV SA14-14-2 vaccine conferred cross-protection against ZIKV challenge in mice. • T cell immunity rather than antibody mediated the cross-protection. • It provides important information in terms of ZIKV prevention or precaution

On the Measurement of Gas Holdup Distribution Near the Region of Impeller in a Gas-Liquid Stirred Rushton Tank by Means of Γ-CT

Three Flow Patterns of Flooding, Loading and Complete Recirculation in a Gas-Liquid Stirred Rushton Tank Were Identified based on Experimental Observation. the Gas-Liquid System Was Composed of Air and Water. under Different Operating Conditions of Gas Flow Rate and Impeller Rotating Speed, the Distribution of Gas Holdup Near the Region of Impeller Was Measured using a Γ-CT Scan Method. Both Quantitative Digital Distribution Curves of Gas Holdup and their Qualitative Color CT Images Were Obtained. at the Region of Impeller, There Was a Convex Characteristic Peak of Gas Holdup Distribution Both in Radial and in Axial Directions, and with the Region Being Gradually Away from the Impeller, the Distribution of Gas Holdup Became Flatter. the Values of Gas Holdup in S33 Regime Were a Little Higher Than Those in L33 Regime. Higher Impeller Rotating Speed Had Some Effect on the Increasing of Gas Holdup at the Region of Higher Axial Height. the Experimental Measurement Results Were Basically Consistent with Those Previously Published by Bombač. the Hole Number and Diameter of Sparger Had Little Influence on the Distribution of Gas Holdup, While the Sparger\u27s Installed Height Had Significant Influence on Them. When the Sparger Was Installed Close to the Bottom of Rushton Tank, a Comparatively Smoother Distribution of Gas Holdup above the Space of Impeller Could Be Obtained. the Research Results in This Paper Were Useful for Better Understanding of Gas Holdup Distribution Near the Region of Impeller of Rushton Tank and Could Also Provide Experimental Data for CFD Simulation. © 2012 Elsevier B.V

Depletion of OLFM4 gene inhibits cell growth and increases sensitization to hydrogen peroxide and tumor necrosis factor-alpha induced-apoptosis in gastric cancer cells

<p>Abstract</p> <p>Background</p> <p>Human olfactomedin 4 (OLFM4) gene is a secreted glycoprotein more commonly known as the anti-apoptotic molecule GW112. OLFM4 is found to be frequently up-regulated in many types of human tumors including gastric cancer and it was believed to play significant role in the progression of gastric cancer. Although the function of OLFM4 has been indicated in many studies, recent evidence strongly suggests a cell or tissue type-dependent role of OLFM4 in cell growth and apoptosis. The aim of this study is to examine the role of gastric cancer-specific expression of OLFM4 in cell growth and apoptosis resistance.</p> <p>Methods</p> <p>OLFM4 expression was eliminated by RNA interference in SGC-7901 and MKN45 cells. Cell proliferation, anchorage-independent growth, cell cycle and apoptosis were characterized in vitro. Tumorigenicity was analyzed in vivo. The apoptosis and caspase-3 activation in response to hydrogen peroxide (H₂O₂) or tumor necrosis factor-alpha (TNF α) were assessed in the presence or absence of caspase inhibitor Z-VAD-fmk.</p> <p>Results</p> <p>The elimination of OLFM4 protein by RNA interference in SGC-7901 and MKN45 cells significantly inhibits tumorigenicity both in vitro and in vivo by induction of cell G1 arrest (all P < 0.01). OLFM4 knockdown did not trigger obvious cell apoptosis but increased H₂O₂or TNF α-induced apoptosis and caspase-3 activity (all P < 0.01). Treatment of Z-VAD-fmk attenuated caspase-3 activity and significantly reversed the H₂O₂or TNF α-induced apoptosis in OLFM4 knockdown cells (all P < 0.01).</p> <p>Conclusion</p> <p>Our study suggests that depletion of OLFM4 significantly inhibits tumorigenicity of the gastric cancer SGC-7901 and MKN45 cells. Blocking OLFM4 expression can sensitize gastric cancer cells to H₂O₂or TNF α treatment by increasing caspase-3 dependent apoptosis. A combination strategy based on OLFM4 inhibition and anticancer drugs treatment may provide therapeutic potential in gastric cancer intervention.</p

Genetic Polymorphisms In Estrogen-related Genes And The Risk Of Breast Cancer Among Han Chinese Women

Exposure to high levels of estrogen is considered an important risk factor for susceptibility to breast cancer. Common polymorphisms in genes that affect estrogen levels may be associated with breast cancer risk, but no comprehensive study has been performed among Han Chinese women. In the present study, 32 single-nucleotide polymorphisms (SNPs) in estrogen-related genes were genotyped using the MassARRAY IPLEX platform in 1076 Han Chinese women. Genotypic and allelic frequencies were compared between case and control groups. Unconditional logistic regression was used to assess the effects of SNPs on breast cancer risk. Associations were also evaluated for breast cancer subtypes stratified by estrogen receptor (ER) and progesterone receptor (PR) status. Case-control analysis showed a significant relation between heterozygous genotypes of rs700519 and rs2069522 and breast cancer risk (OR = 0.723, 95% CI = 0.541-0.965, p = 0.028 and OR = 1.500, 95% CI = 1.078-2.087, p = 0.016, respectively). Subgroup comparisons revealed that rs2446405 and rs17268974 were related to ER status, and rs130021 was associated with PR status. Our findings suggest that rs700519 and rs2069522 are associated with susceptibility to breast cancer among the Han Chinese population and have a cumulative effect with three other identified SNPs. Further genetic and functional studies are needed to identify additional SNPs, and to elucidate the underlying molecular mechanisms

Cross-Protection Against Four Serotypes of Dengue Virus in Mice Conferred by a Zika DNA Vaccine

Both Zika virus (ZIKV) and four serotypes of dengue virus (DENV1–4) are antigenically related mosquito-borne flaviviruses that co-circulate in overlapping geographic distributions. The considerable amino acid sequence homology and structural similarities between ZIKV and DENV1–4 may be responsible for the complicated immunological cross-reactivity observed for these viruses. Thus, a successful Zika vaccine needs to not only confer protection from ZIKV infection but must also be safe during secondary exposures with other flavivirus, especially DENVs. In this study, we used a Zika DNA vaccine candidate (pV-ZME) expressing the ZIKV premembrane and envelop proteins to immunize BALB/c mice and evaluated the potential cross-reactive immune responses to DENV1–4. We observed that three doses of the pV-ZME vaccine elicited the production of cross-reactive antibodies, cytokines and CD8+ T cell responses and generated cross-protection against DENV1–4. Our results demonstrate a novel approach for design and development of safe Zika and/or dengue vaccines