32 research outputs found

    Patient-Specific Unicompartmental Knee Resurfacing Arthroplasty: Use of a Novel Interference Lock to Reduce Tibial Insert Micromotion and Backside Wear

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    Micromotion has long been associated with wear of polyethylene tibial inserts, potentially causing failure of unicompartmental knee replacement systems. One cause of micromotion is the locking mechanism between the undersurface of the polyethylene and the tibial tray. The objective of this study was to investigate the use of new novel lock designs for reducing the micromotion associated with a patient specific tibial implant. Micromotion occurring between the tibial insert and tibial tray was measured using the DVRT method for two new lock designs and compared to the micromotion measured for the prior generation lock design. In total, 18 samples were tested, six in each of the three designs: prior generation CLEARANCE lock design, new LINE-TO-LINE design, new INTERFERENCE design

    Potent and broad HIV-neutralizing antibodies in memory B cells and plasma

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    Induction of broadly neutralizing antibodies (bnAbs) is a goal of HIV-1 vaccine development. Antibody 10E8, reactive with the distal portion of the membrane-proximal external region (MPER) of HIV-1 gp41, is broadly neutralizing. However, the ontogeny of distal MPER antibodies and the relationship of memory B cell to plasma bnAbs are poorly understood. HIV-1–specific memory B cell flow sorting and proteomic identification of anti-MPER plasma antibodies from an HIV-1–infected individual were used to isolate broadly neutralizing distal MPER bnAbs of the same B cell clonal lineage. Structural analysis demonstrated that antibodies from memory B cells and plasma recognized the envelope gp41 bnAb epitope in a distinct orientation compared with other distal MPER bnAbs. The unmutated common ancestor of this distal MPER bnAb was autoreactive, suggesting lineage immune tolerance control. Construction of chimeric antibodies of memory B cell and plasma antibodies yielded a bnAb that potently neutralized most HIV-1 strains

    Plastome phylogenomics of sugarcane and relatives confirms the segregation of the genus Tripidium (Poaceae: Andropogoneae)

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    Sugarcane (Saccharum officinarum) is one of the most important crops inthe world and a major source of sugar for human consumption. Despite this immense value, the circumscription of the genus Saccharum is complex, contentious, and largely unresolved. Saccharum is accepted in a broad sense by some authors or split into various genera such as Erianthus and Tripidium. A plastome phylogenomic analysis of sugarcane and relatives was performed in order to investigate generic delimitation, with emphasis on Tripidium (= Erianthus sect. Ripidium). Our plastome phylogenomics clearly demonstrates that Saccharum s.l. is polyphyletic and Tripidium (distributed in Old World) belongs to a distinct lineage from Saccharum s.s. (Old World) and Erianthus s.s. (= Erianthus sect. Erianthus, New World). Therefore, the present analysis confirms the recognition of Tripidium as a distinct genus from Saccharum and Erianthus, which is also supported by morphology and nuclear markers. The circumscription of Erianthus s.s. remains unclear since our plastome phylogenomics is consistent with either considering it as a distinct genus or including it in Saccharum. Better understanding of the evolutionary relationships of sugarcane and relatives may be useful for the selection of potential taxa for interspecific and intergeneric crosses in the genetic improvement of sugarcane. A taxonomic treatment of the six species of Tripidium is also presented, including descriptions, illustrations, data on geographical distribution, and three new nomenclatural combinations.Fil: Welker, Cassiano A. D.. Universidade Federal de UberlĂąndia; BrasilFil: McKain, Michael R.. University of Alabama at Birmingahm; Estados UnidosFil: Vorontsova, Maria S.. Royal Botanic Gardens; Reino UnidoFil: Peichoto, Myriam Carolina. Consejo Nacional de Investigaciones CientĂ­ficas y TĂ©cnicas. Centro CientĂ­fico TecnolĂłgico Conicet - Nordeste. Instituto de BotĂĄnica del Nordeste. Universidad Nacional del Nordeste. Facultad de Ciencias Agrarias. Instituto de BotĂĄnica del Nordeste; ArgentinaFil: Kellogg, Elizabeth Anne. Donald Danforth Plant Science Center; Estados Unido

    Comparison among total knee arthroplasties with a mobile bearing: menisci versus rotating platform versus AP glide platform

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    A retrospective study was conducted on 60 patients (53 females, seven males with a mean age of 68 years and 5 months) who underwent a total knee replacement using a mobile bearing. The diagnosis was primary osteoarthritis in 57 cases and rheumatoid arthritis in three cases. None of the patients underwent a bilateral procedure, thus 60 implants (33 all cementless, three all cemented, 24 with only the tibial component cemented) were considered. Three different groups were identified: Group 1: first 20 total knee arthroplasties with menisci. Group 2: first 20 total knee arthroplasties with rotating platform. Group 3: first 20 total knee arthroplasties with AP glide platform. Clinical and radiological results at the final follow up, although different in time among the three groups, have shown no revision due to mechanical or septic reasons, and no signs of impending failure

    Immunogenicity of NYVAC Prime-Protein Boost Human Immunodeficiency Virus Type 1 Envelope Vaccination and Simian-Human Immunodeficiency Virus Challenge of Nonhuman Primates.

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    A preventive human immunodeficiency virus type 1 (HIV-1) vaccine is an essential part of the strategy to eradicate AIDS. A critical question is whether antibodies that do not neutralize primary isolate (tier 2) HIV-1 strains can protect from infection. In this study, we investigated the ability of an attenuated poxvirus vector (NYVAC) prime-envelope gp120 boost to elicit potentially protective antibody responses in a rhesus macaque model of mucosal simian-human immunodeficiency virus (SHIV) infection. NYVAC vector delivery of a group M consensus envelope, trivalent mosaic envelopes, or a natural clade B isolate B.1059 envelope elicited antibodies that mediated neutralization of tier 1 viruses, cellular cytotoxicity, and phagocytosis. None of the macaques made neutralizing antibodies against the tier 2 SHIV SF162P3 used for mucosal challenge. Significant protection from infection was not observed for the three groups of vaccinated macaques compared to unvaccinated macaques, although binding antibody to HIV-1 Env correlated with decreased viremia after challenge. Thus, NYVAC Env prime-gp120 boost vaccination elicited polyfunctional, nonneutralizing antibody responses with minimal protective activity against tier 2 SHIV mucosal challenge. <b>IMPORTANCE</b> The antibody responses that confer protection against HIV-1 infection remain unknown. Polyfunctional antibody responses correlated with time to infection in previous macaque studies. Determining the ability of vaccines to induce these types of responses is critical for understanding how to improve upon the one efficacious human HIV-1 vaccine trial completed thus far. We characterized the antibody responses induced by a NYVAC-protein vaccine and determined the protective capacity of polyfunctional antibody responses in an R5, tier 2 mucosal SHIV infection model
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