Inducing Cross-Clade Neutralizing Antibodies against HIV-1 by Immunofocusing

Background: Although vaccines are important in preventing viral infections by inducing neutralizing antibodies (nAbs), HIV-1 has proven to be a difficult target and escapes humoral immunity through various mechanisms. We sought to test whether HIV-1 Env mimics may serve as immunogens. Methodology/Principal Findings: Using random peptide phage display libraries, we identified the epitopes recognized by polyclonal antibodies of a rhesus monkey that had developed high-titer, broadly reactive nAbs after infection with a simianhuman immunodeficiency virus (SHIV) encoding env of a recently transmitted HIV-1 clade C (HIV-C). Phage peptide inserts were analyzed for conformational and linear homology using computational analysis; some peptides mimicked various domains of the original HIV-C Env, such as conformational V3 loop epitopes and the conserved linear region of the gp120 C-terminus. Next, we devised a novel prime/boost strategy to test the immunogenicity of such phage-displayed peptides and primed mice only once with HIV-C gp160 DNA followed by boosting with mixtures of recombinant phages. Conclusions/Significance: This strategy, which was designed to focus the immune system on a few Env epitopes (immunofocusing), not only induced HIV-C gp160 binding antibodies and cross-clade nAbs, but also linked a conserved HIV Env region for the first time to the induction of nAbs: the C-terminus of gp120. The identification of conserved antige

Lattice Thermal Boundary Resistance

Control and modelling of thermal transport at the nanoscale has emerged either as a key issue in modern nanoscience or as a compelling demand for the ever- increasing miniaturization process in information technologies: here the thermal budget of nanodevices is basically ruled over by heat exchanges across interfaces, and the relevant physics is cast in terms of a thermal boundary resistance. In this chapter, we present a unified discussion about the fundamental knowledge developed in this framework. Starting from the most general thermodynamical description of an interface, where the driving force for heat transport is identified together with the actual location and thickness of the interface itself, we define what the thermal boundary resistance is in fact. We then delve into the most successful modelling approaches, based either on the phonon picture or on the atomistic picture. Adopting different assumptions and employing different implementation strategies, they offer a complementary description of the physi- cal mechanisms underlying thermal boundary resistance, and they provide useful computational protocols to predict its value in realistic systems

An Invitro Method to Study the Adherence of Bacteria to Saliva-Treated Tooth Enamel Sections

An in vitro bacterial adherence assay which employed human tooth enamel sections precoated with saliva and an epifluorescent staining technique with acridine orange was developed. The assay was used to study the adherence properties of fresh and type strains of the following oral bacterial species: Bacteroides gingivalis, Bacteroides intermedius, Capnocytophaga species, Haemophilus aphrophilus, Actinobacillus actinomycetemcomitans, Peptostreptococcus species, Veillonella species, Actinomyces israelii, Streptococcus salivarius and Streptococcus sanguis. Approximately half of the bacteria tested adhered well to enamel, including the fresh isolates of B. gingivalis, B. intermedius, Veillonella species and S. sanguis. Adherence did not correlate in all cases with the known distribution of these species in vivo. Three-quarters of the fresh strains adhered better than the type strains of the same species. The assay method is an alternative to the widely used hydroxyapatite bead assay.link_to_subscribed_fulltex