RESUMO
Herpes simplex virus (HSV) infection can cause inflammatory reactions and angiogenesis of the cornea, which significantly reduce corneal transparency. Herpes stromal keratitis (HSK) is an immune mediated disease caused by HSV infection, and is associated with inflammation and angiogenesis of the cornea. It is difficult to control HSK therapeutically. Repeated episodes of HSK can result in chronic inflammatory disease in the corneal stroma. Neovascularization plays a key role in the pathogenesis of HSK, so inhibiting the angiogenesis will help to control HSK disease. In this review, the pathomechanism of HSK is described. The roles of multiple cytokines and soluble mediators in corneal vascularization are discussed, and the potential ways of preventing and controlling corneal vascularization induced by HSK are summarized. (Chin J Ophthalmol, 2019, 55:956-960).
Assuntos
Neovascularização da Córnea , Ceratite Herpética , Neovascularização Patológica , Córnea , Substância Própria , Humanos , Ceratite Herpética/fisiopatologiaRESUMO
The electrical and magnetic properties of Zn-doped Fe(3)O(4) at different doping concentrations of Zn have been investigated using a density functional method with generalized-gradient approximation corrected for on-site Coulombic interactions. The electronic structure calculation predicts that Zn(x)Fe(3-x)O(4) (0 ≤x≤ 0.875) is half-metallic with a full spin polarization. The hopping carrier concentration of Zn(x)Fe(3-x)O(4) decreases with increasing x, which indicates a distinct increase in the resistivity. The saturation magnetization of Zn(x)Fe(3-x)O(4) increases evidently with increasing x from x = 0 to x = 0.75 (i.e. from 4.0 to 8.3 µ(B)/f.u.) and then decreases rapidly to zero at x = 1. The robust half-metallicity, large tunability of electrical and magnetic properties of a Zn doped Fe(3)O(4) system make it a promising functional material for spintronic applications.