367 research outputs found
Atom in a coherently controlled squeezed vacuum
A broadband squeezed vacuum photon field is characterized by a complex
squeezing function. We show that by controlling the wavelength dependence of
its phase it is possible to change the dynamics of the atomic polarization
interacting with the squeezed vacuum. Such a phase modulation effectively
produces a finite range temporal interaction kernel between the two quadratures
of the atomic polarization yielding the change in the decay rates as well as
the appearance of additional oscillation frequencies. We show that decay rates
slower than the spontaneous decay rate can be achieved even for a squeezed bath
in the classic regime. For linear and quadratic phase modulations the power
spectrum of the scattered light exhibits narrowing of the central peak due to
the modified decay rates. For strong phase modulations side lobes appear
symmetrically around the central peak reflecting additional oscillation
frequencies.Comment: 4 pages, 4 figure
Control of Raman Lasing in the Nonimpulsive Regime
We explore coherent control of stimulated Raman scattering in the
nonimpulsive regime. Optical pulse shaping of the coherent pump field leads to
control over the stimulated Raman output. A model of the control mechanism is
investigated.Comment: 4 pages, 5 figure
Retinal nerve fiber layer thickness in subgroups of multiple sclerosis, measured by optical coherence tomography and scanning laser polarimetry
Optical coherence tomography (OCT) and scanning laser polarimetry (GDx ECC) are non-invasive methods used to assess retinal nerve fiber layer (RNFL) thickness, which may be a reliable tool used to monitor axonal loss in multiple sclerosis (MS). The objectives of this study are (1) to compare OCT with the GDx ECC; (2) to assess and compare the RNFL thickness in subgroups of MS. Ophthalmologic examination and RNFL assessment by OCT and GDx were performed in 65 MS patients (26 relapsing-remitting (RRMS), ten secondary-progressive (SPMS), 29 primary-progressive (PPMS)). Twenty-eight patients (43%) had a history of optic neuritis (ON). Adjustments were made for age and disease duration. RNFL thickness was reduced in eyes with previous ON (p < 0.01). No differences were found between PPMS and relapse-onset MS. OCT and GDx ECC measurements were moderately correlated (rho = 0.73, p < 0.01). Visual field-mean deviation (MD) values correlated with OCT means (r = 0.44, p < 0.01) and GDx ECC TSNIT average (r = 0.41, p < 0.01). In patients without previous ON, EDSS correlated with MD (r = -0.36, p < 0.01), visual field-pattern standard deviation (PSD) (r = 0.30, p < 0.05), OCT means (r = -0.31-0.30, p < 0.05) and macular volume (r = -0.37, p < 0.01). For MSIS-29 physical impact score, significant correlations were found with MD (r = -0.48, p < 0.01) and PSD (r = 0.48, p < 0.01). Conclusions: No differences between PPMS and relapse-onset MS subgroups were found. RNFL thickness was reduced in eyes with previous ON. Although OCT and GDx ECC findings were moderately correlated and showed significant correlations with measures of visual function in patients without previous ON, EDSS correlated significantly with visual and OCT measures, but not with GDx ECC
Immune Curbing of Cancer Stem Cells by CTLs Directed to NANOG
Cancer stem cells (CSCs) have been identified as the source of tumor growth and disease recurrence. Eradication of CSCs is thus essential to achieve durable responses, but CSCs are resistant to current anti-tumor therapies. Novel therapeutic approaches that specifically target CSCs will, therefore, be crucial to improve patient outcome. Immunotherapies, which boost the body’s own immune system to eliminate cancerous cells, could be an alternative approach to target CSCs. Vaccines of dendritic cells (DCs) loaded with tumor antigens can evoke highly specific anti-tumor T cell responses. Importantly, DC vaccination also promotes immunological memory formation, paving the way for long-term cancer control. Here, we propose a DC vaccination that specifically targets CSCs. DCs loaded with NANOG peptides, a protein required for maintaining stem cell properties, could evoke a potent anti-tumor immune response against CSCs. We hypothesize that the resulting immunological memory will also control newly formed CSCs, thereby preventing disease recurrence
FAST CARS: Engineering a Laser Spectroscopic Technique for Rapid Identification of Bacterial Spores
Airborne contaminants, e.g., bacterial spores, are usually analyzed by time
consuming microscopic, chemical and biological assays. Current research into
real time laser spectroscopic detectors of such contaminants is based on e.g.
resonant Raman spectroscopy. The present approach derives from recent
experiments in which atoms and molecules are prepared by one (or more) coherent
laser(s) and probed by another set of lasers. The connection with previous
studies based on "Coherent Anti-Stokes Raman Spectroscopy" (CARS) is to be
noted. However generating and utilizing maximally coherent oscillation in
macromolecules having an enormous number of degrees of freedom is much more
challenging. This extension of the CARS technique is called FAST CARS
(Femtosecond Adaptive Spectroscopic Techniques for Coherent Anti-Stokes Raman
Spectroscopy), and the present paper proposes and analyses ways in which it
could be used to rapidly identify pre-selected molecules in real time.Comment: 43 pages, 21 figures; replacement with references added. Submitted to
the Proceedings of National Academy of Science
Spontaneous Regression of Ovarian Carcinoma After Septic Peritonitis; A Unique Case Report
Despite advances in therapy, ovarian cancer remains the most lethal gynecological malignancy and prognosis has not substantially improved over the past 3 decades. Immunotherapy is a promising new treatment option. However, the immunosuppressive cancer microenvironment must be overcome for immunotherapy to be successful. Here, we present a unique case of spontaneous regression of ovarian carcinoma after septic peritonitis. A 79-year-old woman was diagnosed with stage IIIc ovarian cancer. The omental cake biopsy was complicated by sepsis. Although the patient recovered, her physical condition did not allow further treatment for her ovarian cancer. After 6 months, spontaneous regression of the tumor was observed during surgery. Analysis of the immune infiltrate in the tissues showed a shift from a pro-tumorigenic to an anti-tumorigenic immune response after sepsis. Strong activation of the immune system during sepsis overruled the immunosuppressive tumor microenvironment and allowed for a potent anti-tumor immune response. More understanding of immunological responses in cases with cancer and septic peritonitis might be crucial to identify potential new targets for immunotherapy
Survival of Ovarian Cancer Patients Is Independent of the Presence of DC and T Cell Subsets in Ascites
Ascites is a prominent feature of ovarian cancer and could serve as liquid biopsy to assess the immune status of patients. Tumor-infiltrating T lymphocytes are correlated with improved survival in ovarian cancer. To investigate whether immune cells in ascites are associated with patient outcome, we analyzed the amount of dendritic cell (DC) and T cell subsets in ascites from ovarian cancer patients diagnosed with high-grade serous cancer (HGSC). Ascites was collected from 62 HGSC patients prior to chemotherapy. Clinicopathological, histological and follow-up data from patients were collected. Ascites-derived immune cells were isolated using density-gradient centrifugation. The presence of myeloid DCs (BDCA-1+, BDCA-3+, CD16+), pDCs (CD123+BDCA-2+), and T cells (CD4+, CD8+) was analyzed using flow cytometry. Complete cytoreduction, response to primary treatment and chemosensitivity were associated with improved patient outcome. In contrast, immune cells in ascites did not significantly correlate with patient survival. However, we observed a trend toward improved outcome for patients having low percentages of CD4+ T cells. Furthermore, we assessed the expression of co-stimulatory and co-inhibitory molecules on T cells and non-immune cells in 10 ascites samples. PD-1 was expressed by 30% of ascites-derived T cells and PD-L1 by 50% of non-immune cells. However, the percentage of DC and T cell subsets in ascites was not directly correlated to the survival of HGSC patients
Beta-delayed proton emission in the 100Sn region
Beta-delayed proton emission from nuclides in the neighborhood of 100Sn was
studied at the National Superconducting Cyclotron Laboratory. The nuclei were
produced by fragmentation of a 120 MeV/nucleon 112Sn primary beam on a Be
target. Beam purification was provided by the A1900 Fragment Separator and the
Radio Frequency Fragment Separator. The fragments of interest were identified
and their decay was studied with the NSCL Beta Counting System (BCS) in
conjunction with the Segmented Germanium Array (SeGA). The nuclei 96Cd, 98Ing,
98Inm and 99In were identified as beta-delayed proton emitters, with branching
ratios bp = 5.5(40)%, 5.5+3 -2%, 19(2)% and 0.9(4)%, respectively. The bp for
89Ru, 91,92Rh, 93Pd and 95Ag were deduced for the first time with bp = 3+1.9
-1.7%, 1.3(5)%, 1.9(1)%, 7.5(5)% and 2.5(3)%, respectively. The bp = 22(1)% for
101Sn was deduced with higher precision than previously reported. The impact of
the newly measured bp values on the composition of the type-I X-ray burst ashes
was studied.Comment: 15 pages, 14 Figures, 4 Table
MAPK Signaling Determines Anxiety in the Juvenile Mouse Brain but Depression-Like Behavior in Adults
MAP kinase signaling has been implicated in brain development, long-term memory, and the response to antidepressants. Inducible Braf knockout mice, which exhibit protein depletion in principle forebrain neurons, enabled us to unravel a new role of neuronal MAPK signaling for emotional behavior. Braf mice that were induced during adulthood showed normal anxiety but increased depression-like behavior, in accordance with pharmacological findings. In contrast, the inducible or constitutive inactivation of Braf in the juvenile brain leads to normal depression-like behavior but decreased anxiety in adults. In juvenile, constitutive mutants we found no alteration of GABAergic neurotransmission but reduced neuronal arborization in the dentate gyrus. Analysis of gene expression in the hippocampus revealed nine downregulated MAPK target genes that represent candidates to cause the mutant phenotype
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