LPS is a main causative agent of septic shock. There is a lack of effective therapies. In vitro studies have shown that uptake of apoptotic cells actively inhibits the secretion by activated macrophages (M) of proinflammatory mediators such as TNF- and that such uptake increases the antiinflammatory and immunosuppressive cytokine TGF-. We therefore investigated the protective effect of apoptotic cells against LPS-induced endotoxic shock in mice. The current report is the first study to demonstrate that administration of apoptotic cells can protect mice from LPS-induced death, even when apoptotic cells were administered 24 h after LPS challenge. The beneficial effects of administration of apoptotic cells included 1) reduced circulating proinflammatory cytokines, 2) suppression of polymorphonuclear neutrophil infiltration in target organs, and 3) decreased serum LPS levels. LPS can quickly bind to apoptotic cells

We derive the asymptotic distributions of the spiked eigenvalues and eigenvectors under a generalized and unified asymptotic regime, which takes into account the spike magnitude of leading eigenvalues, sample size, and dimensionality. This new regime allows high dimensionality and diverging eigenvalue spikes and provides new insights into the roles the leading eigenvalues, sample size, and dimensionality play in principal component analysis. The results are proven by a technical device, which swaps the role of rows and columns and converts the high-dimensional problems into low-dimensional ones. Our results are a natural extension of those in Paul (2007) to more general setting with new insights and solve the rates of convergence problems in Shen et al.(2013). They also reveal the biases of the estimation of leading eigenvalues and eigenvectors by using principal component analysis, and lead to a new covariance estimator for the approximate factor model, called shrinkage principal orthogonal complement thresholding (S-POET), that corrects the biases. Our results are successfully applied to outstanding problems in estimation of risks of large portfolios and false discovery proportions for dependent test statistics and are illustrated by simulation studies.

No abstract uploaded!

Turkish J. Math. 25 (2001), no. 1, 195–236.

Strongly pseudoconvex CR manifolds are boundaries of Stein varieties with isolated normal singularities.We prove that any nonconstant CR morphism between two (2n.1)-dimensional strongly pseudoconvex CR manifolds lying in an n-dimensional Stein variety with isolated singularities are necessarily a CR biholomorphism. As a corollary, we prove that any nonconstant self map of (2n . 1)-dimensional strongly pseudoconvex CR manifold is a CR automorphism. We also prove that a finite ′etale covering map between two resolutions of isolated normal singularities must be an isomorphism.