47 research outputs found
Defects and glassy dynamics in solid He-4: Perspectives and current status
We review the anomalous behavior of solid He-4 at low temperatures with
particular attention to the role of structural defects present in solid. The
discussion centers around the possible role of two level systems and structural
glassy components for inducing the observed anomalies. We propose that the
origin of glassy behavior is due to the dynamics of defects like dislocations
formed in He-4. Within the developed framework of glassy components in a solid,
we give a summary of the results and predictions for the effects that cover the
mechanical, thermodynamic, viscoelastic, and electro-elastic contributions of
the glassy response of solid He-4. Our proposed glass model for solid He-4 has
several implications: (1) The anomalous properties of He-4 can be accounted for
by allowing defects to freeze out at lowest temperatures. The dynamics of solid
He-4 is governed by glasslike (glassy) relaxation processes and the
distribution of relaxation times varies significantly between different
torsional oscillator, shear modulus, and dielectric function experiments. (2)
Any defect freeze-out will be accompanied by thermodynamic signatures
consistent with entropy contributions from defects. It follows that such
entropy contribution is much smaller than the required superfluid fraction, yet
it is sufficient to account for excess entropy at lowest temperatures. (3) We
predict a Cole-Cole type relation between the real and imaginary part of the
response functions for rotational and planar shear that is occurring due to the
dynamics of defects. Similar results apply for other response functions. (4)
Using the framework of glassy dynamics, we predict low-frequency yet to be
measured electro-elastic features in defect rich He-4 crystals. These
predictions allow one to directly test the ideas and very presence of glassy
contributions in He-4.Comment: 33 pages, 13 figure
The rise of \u27women\u27s poetry\u27 in the 1970s an initial survey into new Australian poetry, the women\u27s movement, and a matrix of revolutions
Fc-Optimized Anti-CD25 Depletes Tumor-Infiltrating Regulatory T Cells and Synergizes with PD-1 Blockade to Eradicate Established Tumors
CD25 is expressed at high levels on regulatory TÂ (Treg) cells and was initially proposed as a target for cancer immunotherapy. However, anti-CD25 antibodies have displayed limited activity against established tumors. We demonstrated that CD25 expression is largely restricted to tumor-infiltrating Treg cells in mice and humans. While existing anti-CD25 antibodies were observed to deplete Treg cells in the periphery, upregulation of the inhibitory Fc gamma receptor (FcÎłR) IIb at the tumor site prevented intra-tumoral Treg cell depletion, which may underlie the lack of anti-tumor activity previously observed in pre-clinical models. Use of an anti-CD25 antibody with enhanced binding to activating FcÎłRs led to effective depletion of tumor-infiltrating Treg cells, increased effector to Treg cell ratios, and improved control of established tumors. Combination with anti-programmed cell death protein-1 antibodies promoted complete tumor rejection, demonstrating the relevance of CD25 as a therapeutic target and promising substrate for future combination approaches in immune-oncology
Genome-wide association study identifies two susceptibility loci for osteosarcoma
Osteosarcoma is the most common primary bone malignancy of adolescents and young adults. To better understand the genetic etiology of osteosarcoma, we performed a multistage genome-wide association study consisting of 941 individuals with osteosarcoma (cases) and 3,291 cancer-free adult controls of European ancestry. Two loci achieved genome-wide significance: a locus in the GRM4 gene at 6p21.3 (encoding glutamate receptor metabotropic 4; rs1906953; P = 8.1 Ă 10â»âč) and a locus in the gene desert at 2p25.2 (rs7591996 and rs10208273; P = 1.0 Ă 10â»âž and 2.9 Ă 10â»â·, respectively). These two loci warrant further exploration to uncover the biological mechanisms underlying susceptibility to osteosarcoma
Improving Vaccine-Induced Immunity: Can Baseline Predict Outcome?
Immune signatures measured at baseline and immediately prior to vaccination may predict the immune response to vaccination. Such pre-vaccine assessment might allow not only population-based, but also more personalized vaccination strategies (âprecision vaccinationâ). If baseline immune signatures are predictive, the underlying mechanism they reflect may also determine vaccination outcome. Thus, baseline signatures might contribute to identifying interventional targets to be modulated prior to vaccination in order to improve vaccination responses. This concept has the potential to transform vaccination strategies and usher in a new approach to improve global health.SCOPUS: re.jinfo:eu-repo/semantics/publishe
Antibody Engineering & Therapeutics 2015: The Antibody Society's annual meeting December 7-10, 2015, San Diego, CA
Stemcel biology/Regenerative medicine (incl. bloodtransfusion