Printing of Large-Scale, Flexible, Long-Term Stable Dielectric Mirrors with Suppressed Side Interferences

Dielectric mirrors are wavelength-selective mirrors which are based on thin film interference effects. Their optical band can precisely be adjusted in width, position, and reflectance by the refractive index of the applied materials, the layers' thicknesses, and the amount of deposited layers. Nowadays, they are a well-known light management tool for efficiency enhancement in, for example, semitransparent organic solar cells (OSCs) and light guiding in organic light-emitting diodes (OLEDs). However, most of the dielectric mirrors are still fabricated by lab-scale techniques such as spin-coating or physical vapor deposition under vacuum. Large-scale, fully printed (maximum 20 x 20 cm(2)) dielectric mirrors with adjustable reflectance characteristics are fabricated, using temperatures of maximum 50 degrees C and alcohol-based inks. According to the moderate processing conditions they can be easily deposited not only on rigid glass substrates but also on flexible foils. They show high stability against humidity, light irradiation, and temperature, positioning themselves as good candidates for applications in OLEDs and OSCs. Eventually, by simulations and experiments it is verified that a moderate degree of variations in layer thickness and surface roughness can suppress side interference fringes, while not impacting the main transmittance minimum or the main reflection maximum, respectively

Wild-Type Measles Virus Interferes with Short-Term Engraftment of Human CD34+ Hematopoietic Progenitor Cells ▿

Transient lymphopenia is a hallmark of measles virus (MV)-induced immunosuppression. To address to what extent replenishment of the peripheral lymphocyte compartment from bone marrow (BM) progenitor/stem cells might be affected, we analyzed the interaction of wild-type MV with hematopoietic stem and progenitor cells (HS/PCs) and stroma cells in vitro. Infection of human CD34+ HS/PCs or stroma cells with wild-type MV is highly inefficient yet noncytolytic. It occurs independently of CD150 in stroma cells but also in HS/PCs, where infection is established in CD34+ CD150− and CD34+ CD150+ (in humans representing HS/PC oligopotent precursors) subsets. Stroma cells and HS/PCs can mutually transmit MV and may thereby create a possible niche for continuous viral exchange in the BM. Infected lymphocytes homing to this compartment may serve as sources for HS/PC or stroma cell infection, as reflected by highly efficient transmission of MV from both populations in cocultures with MV-infected B or T cells. Though MV exposure does not detectably affect the viability, expansion, and colony-forming activity of either CD150+ or CD150− HS/PCs in vitro, it efficiently interferes with short- but not long-term hematopoietic reconstitution in NOD/SCID mice. Altogether, these findings support the hypothesis that MV accession of the BM compartment by infected lymphocytes may contribute to peripheral blood mononuclear cell lymphopenia at the level of BM suppression