50 research outputs found

    An Investigation of Equivalence Principle Violations Using Solar Neutrino Oscillations in a Constant Gravitational Potential

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    Neutrino oscillations induced by a flavor-dependent violation of the Einstein Equivalence Principle (VEP) have been recently considered as a suitable explanation of the solar electron-neutrino deficiency. Unlike the MSW oscillation mechanism, the VEP mechanism is dependent on a coupling to the local background gravitational potential Φ\Phi. We investigate the differences which arise by considering three-flavor VEP neutrinos oscillating against fixed background potentials, and against the radially-dependent solar potential. This can help determine the sensitivity of the gravitationally-induced oscillations to both constancy and size (order of magnitude) of Φ\Phi. In particular, we consider the potential of the local superculster, Φ=3×105|\Phi|=3\times 10^{-5}, in light of recent work suggesting that the varying solar potential has no effect on the oscillations. The possibility for arbitrarily large background potentials in different cosmologies is discussed, and the effects of one such potential (Φ=103\Phi = 10^{-3}) are considered.Comment: 12pp, LaTeX; 12 figures (bitmapped postscript); Submitted to Phys Rev

    Broadly reactive human CD8 T cells that recognize an epitope conserved between VZV, HSV and EBV

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    Human herpesviruses are important causes of potentially severe chronic infections for which T cells are believed to be necessary for control. In order to examine the role of virus-specific CD8 T cells against Varicella Zoster Virus (VZV), we generated a comprehensive panel of potential epitopes predicted in silico and screened for T cell responses in healthy VZV seropositive donors. We identified a dominant HLA-A*0201-restricted epitope in the VZV ribonucleotide reductase subunit 2 and used a tetramer to analyze the phenotype and function of epitope-specific CD8 T cells. Interestingly, CD8 T cells responding to this VZV epitope also recognized homologous epitopes, not only in the other α-herpesviruses, HSV-1 and HSV-2, but also the γ-herpesvirus, EBV. Responses against these epitopes did not depend on previous infection with the originating virus, thus indicating the cross-reactive nature of this T cell population. Between individuals, the cells demonstrated marked phenotypic heterogeneity. This was associated with differences in functional capacity related to increased inhibitory receptor expression (including PD-1) along with decreased expression of co-stimulatory molecules that potentially reflected their stimulation history. Vaccination with the live attenuated Zostavax vaccine did not efficiently stimulate a proliferative response in this epitope-specific population. Thus, we identified a human CD8 T cell epitope that is conserved in four clinically important herpesviruses but that was poorly boosted by the current adult VZV vaccine. We discuss the concept of a “pan-herpesvirus” vaccine that this discovery raises and the hurdles that may need to be overcome in order to achieve this
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