Types, obstacles and sources of empowerment in co-design: the role of shared material objects and processes

Co-design is intrinsically linked to the notion of empowerment, however little research has focussed specifically on understanding the types, obstacles and sources of empowerment in co-design. This paper combines theoretical investigations with observations derived from co-designed research by academic and non-academic partners to explore these issues, in particular, the role of shared material objects and processes in supporting empowerment during co-design. The paper uses the notions of ‘power over,’ ‘power to’, ‘power with’ and ‘power within’ to tease out different aspects of empowerment, and draws on empirical observations to determine different obstacles and sources associated with each. The study therefore makes a theoretical contribution to the understanding of co-design as an empowerment process and should be useful for design researchers undertaking co-design projects with non-experts

Spin-Orbit Interaction Enhanced Fractional Quantum Hall States in the Second Landau Level

We study the fractional quantum Hall effect at filling fractions 7/3 and 5/2 in the presence of the spin-orbit interaction, using the exact diagonalization method and the density matrix renormalization group (DMRG) method in a spherical geometry. Trial wave functions at these fillings are the Laughlin state and the Moore-Reed-Pfaffian state. The ground state excitation energy gaps and pair-correlation functions at fractional filling factor 7/3 and 5/2 in the second Landau level are calculated. We find that the spin-orbit interaction stabilizes the fractional quantum Hall states.Comment: 4pages, 4figure

Enhancing the immunogenicity of tumour lysate-loaded dendritic cell vaccines by conjugation to virus-like particles

BACKGROUND: Tumour cell lysates are an excellent source of many defined and undefined tumour antigens and have been used clinically in immunotherapeutic regimes but with limited success. METHODS: We conjugated Mel888 melanoma lysates to rabbit haemorrhagic disease virus virus-like particles (VLP), which can act as vehicles to deliver multiple tumour epitopes to dendritic cells (DC) to effectively activate antitumour responses. RESULTS: Virus-like particles did not stimulate the phenotypic maturation of DC although, the conjugation of lysates to VLP (VLP-lysate) did overcome lysate-induced suppression of DC activation. Lysate-conjugated VLP enhanced delivery of antigenic proteins to DC, while the co-delivery of VLP-lysates with OK432 resulted in cross-priming of naïve T cells, with expansion of a MART1(+) population of CD8(+) T cells and generation of a specific cytotoxic response against Mel888 tumour cell targets. The responses generated with VLP-lysate and OK432 were superior to those stimulated by unconjugated lysate with OK432. CONCLUSION: Collectively, these results show that the combination of VLP-lysate with OK432 delivered to DC overcomes the suppressive effects of lysates, and enables priming of naïve T cells with superior ability to specifically kill their target tumour cells

VLPs and particle strategies for cancer vaccines

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Microneedles: A New Frontier in Nanomedicine Delivery

This review aims to concisely chart the development of two individual research fields, namely nanomedicines, with specific emphasis on nanoparticles (NP) and microparticles (MP), and microneedle (MN) technologies, which have, in the recent past, been exploited in combinatorial approaches for the efficient delivery of a variety of medicinal agents across the skin. This is an emerging and exciting area of pharmaceutical sciences research within the remit of transdermal drug delivery and as such will undoubtedly continue to grow with the emergence of new formulation and fabrication methodologies for particles and MN. Firstly, the fundamental aspects of skin architecture and structure are outlined, with particular reference to their influence on NP and MP penetration. Following on from this, a variety of different particles are described, as are the diverse range of MN modalities currently under development. The review concludes by highlighting some of the novel delivery systems which have been described in the literature exploiting these two approaches and directs the reader towards emerging uses for nanomedicines in combination with MN

Limited in vivo reactivity of polyclonal effector cytotoxic T cells towards altered peptide ligands.

T cell responses are regulated by the affinity/avidity of the T cell receptor for the MHC/peptide complex, available costimulation and duration of antigenic stimulation. Altered peptide ligands (APLs) are usually recognized with a reduced affinity/avidity by the T cell receptor and are often able to only partially activate T cells in vitro or may even function as antagonists. Here we assessed the ability of APLs derived from peptide p33 of lymphocytic choriomeningitis virus (LCMV) to mediate lysis of target cells in vivo, confer anti-viral protection and cause auto-immune disease. In general, in vitro cross-reactivity between APLs was rather limited, and even strongly cross-reactive cytotoxic T lymphocytes were only able to mediate moderate anti-viral protection. Partial protection was observed for infection with LCMV or low doses of recombinant vaccinia virus, while no reduced viral titers could be seen upon infection with high dose of vaccinia virus. In a transgenic mouse model expressing LCMV glycoprotein in the islets of the pancreas, APLs induced a transient insulitis but failed to induce autoimmune diabetes. Thus, effector functions induced by even highly homologous APLs are rather limited in vivo

Limited in vivo reactivity of polyclonal effector cytotoxic T cells towards altered peptide ligands.

T cell responses are regulated by the affinity/avidity of the T cell receptor for the MHC/peptide complex, available costimulation and duration of antigenic stimulation. Altered peptide ligands (APLs) are usually recognized with a reduced affinity/avidity by the T cell receptor and are often able to only partially activate T cells in vitro or may even function as antagonists. Here we assessed the ability of APLs derived from peptide p33 of lymphocytic choriomeningitis virus (LCMV) to mediate lysis of target cells in vivo, confer anti-viral protection and cause auto-immune disease. In general, in vitro cross-reactivity between APLs was rather limited, and even strongly cross-reactive cytotoxic T lymphocytes were only able to mediate moderate anti-viral protection. Partial protection was observed for infection with LCMV or low doses of recombinant vaccinia virus, while no reduced viral titers could be seen upon infection with high dose of vaccinia virus. In a transgenic mouse model expressing LCMV glycoprotein in the islets of the pancreas, APLs induced a transient insulitis but failed to induce autoimmune diabetes. Thus, effector functions induced by even highly homologous APLs are rather limited in vivo

\uc1caros de penas e carrapatos (Acari) associados a Turdus albicollis Vieillot (Aves, Muscicapidae) em uma \ue1rea de Mata Atl\ue2ntica da Ilha Grande, Rio de Janeiro, Brasil

O parasitismo é um importante mecanismo que afeta populações e comunidades. O objetivo deste estudo foi investigar a fauna de ectoparasitos que habita o corpo do sabiá-de-coleira, Turdus albicollis Vieillot, 1818 e avaliar se a massa corporal do hospedeiro é afetada por estes parasitos. Os indivíduos de T. albicollis foram mensalmente capturados na Ilha Grande, Rio de Janeiro, no período de julho de 1999 a junho de 2000, em uma área de Floresta Atlântica. As aves foram individualmente marcadas, pesadas e examinadas para registrar e quantificar a presença de ectoparasitos. A abundância e a localização dos parasitos no corpo do hospedeiro foram registradas. Em 54 indivíduos de T. albicollis amostrados, foram encontrados duas espécies de ectoparasitos. A prevalência de ácaros de penas, Pterodectes turdinus Berla, 1959, foi de 72,2% enquanto que a de carrapatos, Amblyomma longirostre Koch, 1844, foi de 27,8%. A abundância mensal de P. turdinus foi significativamente relacionada com os meses do ano, sendo maior nos meses com menor freqüência de chuva. Não houve relação estatisticamente significativa entre a massa corporal do hospedeiro (g) e a abundância total de ácaros de penas e carrapatos.<br>Parasitism is an important mechanism affecting populations and communities. The purpose of this study was to investigate the ectoparasites fauna living on the body of the white-necked trush, Turdus albicollis Vieillot, 1818, and to evaluate if the host body mass is affected by these parasites. Turdus albicollis were monthly captured at Ilha Grande, Rio de Janeiro, from July 1999 to June 2000 in an area of Atlantic Forest. The birds were individualy marked, weighed and carefully checked to record and quantify the presence of ectoparasites. Parasite abundance and location on the bird's body were recorded. In 54 individuals of T. albicollis sampled, two ectoparasite species were found. The prevalence of the feather mite Pterodectes turdinus Berla, 1959, and the tick Amblyomma longirostre Koch, 1844 was 72,2% and 27,8%, respectively. The monthly abundance of P. turdinus was related to the dry and wet months, and it was significantly higher in the dry months than in the wet months. There was no significant relationship between hosts body mass (g) and total abundance of feather mites and ticks