Synthetic Oligosaccharides for Moraxella Vaccine
    74.
    发明申请
    Synthetic Oligosaccharides for Moraxella Vaccine 有权
    Moraxella疫苗的合成寡糖

    公开(公告)号:US20140148592A1

    公开(公告)日:2014-05-29

    申请号:US14171305

    申请日:2014-02-03

    Abstract: The present invention provides synthetic Moraxella catarrhalis lipooligosaccharide (LOS)-based oligosaccharides and conjugates containing various M. catarrhalis serotype-specific oligosaccharide antigens or various core M. catarrhalis oligosaccharide structures or motifs corresponding to one or more of the three major serotypes and/or members within a given serotype. The oligosaccharides may be synthesized by a chemical assembly methodology relying on a limited number of monosaccharide and disaccharide building blocks. The invention further provides M. catarrhalis LOS-based immunogenic and immunoprotective compositions and antibodies derived therefrom for diagnosing, treating, and preventing infections caused by M. catarrhalis.

    Abstract translation: 本发明提供合成的莫拉卡氏菌属低密度脂多糖(LOS)基寡糖和含有各种卡他莫拉胺血清型特异性寡糖抗原或各种核心卡他莫拉低聚糖结构或缀合物的缀合物,其对应于三种主要血清型和/或成员中的一种或多种 在给定的血清型。 寡糖可以通过依靠有限数量的单糖和二糖结构单元的化学组装方法来合成。 本发明进一步提供基于粘膜炎的基于LOS的免疫原性和免疫保护组合物及其衍生的抗体用于诊断,治疗和预防卡他莫拉菌引起的感染。

    Method and compositions for immunotherapy of inflammatory and immune-dysregulatory diseases
    78.
    发明授权
    Method and compositions for immunotherapy of inflammatory and immune-dysregulatory diseases 有权
    免疫治疗炎症和免疫调节疾病的方法和组合物

    公开(公告)号:US08420783B2

    公开(公告)日:2013-04-16

    申请号:US11296432

    申请日:2005-12-08

    Abstract: Methods and compositions for immunotherapy of inflammatory and immune-dysregulatory diseases, using multispecific antagonists that target at least two different markers are disclosed. The different targets include proinflammatory effectors of the innate immune system and targets specifically associated with an inflammatory or immune-dysregulatory disorder, wherein the targets included in the latter group are not a proinflammatory effector of the immune system. Thus, the multispecific antagonist contains at least one binding specificity related to the diseased cell or condition being treated and at least one specificity to a component of the immune system. The multispecific antagonists are used in the treatment of various diseases that are generated or exacerbated by, or otherwise involve, proinflammatory effectors of the innate immune system.

    Abstract translation: 公开了使用靶向至少两种不同标记的多特异性拮抗剂的炎性和免疫调节性疾病的免疫治疗的方法和组合物。 不同的靶标包括先天免疫系统的促炎效应物和与炎症或免疫调节障碍特异性相关的靶标,其中包括在后一组中的靶标不是免疫系统的促炎效应物。 因此,多特异性拮抗剂含有与待治疗的病变细胞或病症相关的至少一种结合特异性,并且对免疫系统的组分具有至少一种特异性。 多特异性拮抗剂用于治疗由天然免疫系统的促炎症作用者产生或加剧或以其他方式涉及的各种疾病。

    Methods For Inducing Autolysis In Infectious Bacteria
    79.
    发明申请
    Methods For Inducing Autolysis In Infectious Bacteria 审中-公开
    诱导感染性细菌自溶的方法

    公开(公告)号:US20130011400A1

    公开(公告)日:2013-01-10

    申请号:US13412218

    申请日:2012-03-05

    Abstract: The present invention relates to methods for the killing of infectious bacteria by modulating the extra-cellular concentration of bacterial cell signalling molecules. This has the effect of inducing rapid cell death (autolysis) in the majority of bacterial cells, and preventing virulence or restoring a benign state in surviving cells. These receptors have applications for the treatment of individuals with susceptibility to infection, the treatment of patients with existing infections, in disease management, and in related applications where the host for infection is an animal or plant. The compositions described herein are particularly relevant to Pseudomonas aeruginosa infection, for example in the treatment of pulmonary infection in cystic fibrosis patients, and represent a unique bactericidal medication that does not directly target the bacteria.

    Abstract translation: 本发明涉及通过调节细菌细胞信号分子的细胞外浓度来杀死感染性细菌的方法。 这具有在大多数细菌细胞中诱导快速细胞死亡(自溶)的作用,并且防止存活细胞中的毒力或恢复良性状态。 这些受体具有用于治疗感染易感性,治疗现有感染患者,疾病管理以及感染宿主是动物或植物的相关应用的个体的应用。 本文描述的组合物与铜绿假单胞菌感染特别相关,例如在囊性纤维化患者中治疗肺部感染,并且代表不直接靶向细菌的独特的杀菌药物。

    Human Antibodies Cross-Reacting With A Bacterial And A Self Antigen From Atherosclerotic Plaques
    80.
    发明申请
    Human Antibodies Cross-Reacting With A Bacterial And A Self Antigen From Atherosclerotic Plaques 审中-公开
    人类抗体与来自动脉粥样硬化斑块的细菌和自身抗原交叉反应

    公开(公告)号:US20120165211A1

    公开(公告)日:2012-06-28

    申请号:US13350527

    申请日:2012-01-13

    Abstract: The present invention refers to human antibodies derived from human antibody libraries prepared from atherosclerotic plaques. It further refers to human antibodies able to immunologically recognize both human transgelin or fragments thereof and a protein with at least 50% similarity to OmpK36 (Outer membrane protein, Klebsiella, K36; GI: 295881594) or fragments thereof. Human transgelin is preferably transgelin 1 (Accession N° Q01995, GI:48255907). The antibodies further recognize an antigen in the atherosclerotic plaque and are useful for the preparation of immunodiagnostic reagents or assays to detect atherogenic diseases. The invention also relates to the use of anti-TAGLN monoclonal antibodies, showing cross-reactivity with a bacterial antigen having at least 50% similarity with OmpK36, for detecting antigens in the atherosclerotic plaque or as atherosclerotic related reagents in an immuno-competition assay.

    Abstract translation: 本发明涉及源自动脉粥样硬化斑块制备的人抗体文库的人抗体。 其还涉及能够免疫识别人类透明质素或其片段的人抗体以及与OmpK36(外膜蛋白,克雷伯氏菌,K36; GI:295881594)或其片段具有至少50%相似性的蛋白质。 人类透明质素优选为透明质素1(登录号:Q01995,GI:48255907)。 抗体进一步识别动脉粥样硬化斑块中的抗原,并且可用于制备免疫诊断试剂或检测致动脉粥样化疾病的测定法。 本发明还涉及使用抗TAGLN单克隆抗体,显示与与OmpK36具有至少50%相似性的细菌抗原的交叉反应性,用于在免疫竞争测定中检测动脉粥样硬化斑块中的抗原或作为动脉粥样硬化相关试剂。

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