Antimultiorganism glycoconjugate vaccine
    32.
    发明授权
    Antimultiorganism glycoconjugate vaccine 有权
    抗肿瘤药物糖缀合疫苗

    公开(公告)号:US07422755B2

    公开(公告)日:2008-09-09

    申请号:US11035884

    申请日:2005-01-18

    摘要: The present invention relates, e.g., to a glycoconjugate composition comprising one or more polysaccharide types from a cell wall polysaccharide preparation from B. pumilus Sh 18, or variants thereof. Also disclosed are antibodies generated against the glycoconjugates, and methods of using the glycoconjugates and antibodies. An antimultiorganism vaccine which reacts against at least Haemophilus influenzae type a, Haemophilus influenzae type b, Staphylococcus aureus, and Staphylococcus epidermidis, is disclosed.

    摘要翻译: 本发明涉及例如包含一种或多种多糖类型的糖缀合物组合物,所述多糖类型来自微生物短小芽孢杆菌Sh18的细胞壁多糖制剂或其变体。 还公开了针对糖缀合物产生的抗体,以及使用糖缀合物和抗体的方法。 公开了至少对流感嗜血杆菌a型,流感嗜血杆菌b型,金黄色葡萄球菌和表皮葡萄球菌进行反应的抗多元素疫苗。

    Lipooligosaccharide based vaccine for prevention of moraxella (branhamella)catarrhalis infections in humans
    33.
    发明授权
    Lipooligosaccharide based vaccine for prevention of moraxella (branhamella)catarrhalis infections in humans 失效
    基于低聚糖的疫苗,用于预防人体中的莫拉氏菌(布氏菌)卡他氏菌感染

    公开(公告)号:US06685949B1

    公开(公告)日:2004-02-03

    申请号:US09610034

    申请日:2000-07-05

    IPC分类号: A61K3902

    摘要: A conjugate vaccine for Moraxella (Branhamella) catarrhalis comprising isolated lipooligosaccharide from which esterified fatty acids have been removed, to produce a detoxified lipooligosaccharide (dLOS), or from which lipid A has been removed, to produce a detoxified oligosaccharide (OS), which is linked to an immunogenic carrier. The vaccine is useful for preventing otitis media and respiratory infections caused by M. catarrhalis in mammals, including humans.

    摘要翻译: 包含分离出的脂多糖的莫拉沙氏菌(Branhamella)卡他氏菌共轭疫苗,其中除去了酯化的脂肪酸,产生脱脂脂寡糖(dLOS),或从其中除去脂质A,产生解毒的寡糖(OS) 与免疫原性载体连接。 该疫苗可用于预防由哺乳动物包括人在内的卡他莫拉菌引起的中耳炎和呼吸道感染。

    Vaccine for shigella
    36.
    发明授权
    Vaccine for shigella 失效
    志贺氏菌疫苗

    公开(公告)号:US08747863B2

    公开(公告)日:2014-06-10

    申请号:US13059051

    申请日:2009-08-14

    摘要: Disclosed are immunogenic conjugates and therapeutic compositions that include such immunogenic conjugates. Also disclosed are methods of treating and/or inhibiting an Shigella sonnei infection. The disclosed immunogenic conjugates have the general structure: Pr—Sr—O—N═C-Kdo-OS wherein Pr is a carrier protein, Sr is an optional spacer moiety, Kdo is an 3-deoxy-D-manno-octulosonic acid or a derivative thereof, and OS is an oligosaccharide or polysaccharide obtained from S. sonnei. In specific examples, the immunogenic conjugates include the core oligosaccharide obtained from S. sonnei having the structure: wherein R is between 1 and 10 disaccharide repeat units. In specific examples, the disaccharide repeat unit included in the immunogenic conjugate has the structure: α-L-AltNAcA-3-β-FucNAc4N-4-.

    摘要翻译: 公开了包括这种免疫原性缀合物的免疫原性缀合物和治疗组合物。 还公开了治疗和/或抑制志贺氏杆菌感染的方法。 所公开的免疫原性缀合物具有以下通用结构:Pr-Sr-O-N = C-Kdo-OS,其中Pr是载体蛋白,Sr是任选的间隔子部分,Kdo是3-脱氧-D-丙氨酸辛酯酸或 其衍生物,OS是从S. sonnei获得的寡糖或多糖。 在具体实例中,免疫原性缀合物包括从具有以下结构的S. sonnei获得的核心寡糖:其中R为1至10个二糖重复单元。 在具体实例中,包含在免疫原性缀合物中的二糖重复单元具有以下结构:α-L-AltNAcA-3-&bgr-FucNAc4N-4-。

    Vaccines against influenza virus
    37.
    发明授权
    Vaccines against influenza virus 失效
    针对流感病毒的疫苗

    公开(公告)号:US08658180B2

    公开(公告)日:2014-02-25

    申请号:US12541804

    申请日:2009-08-14

    摘要: Disclosed are immunogenic conjugates having the general formula: M2e-Cys-S—CH2—C(O)—NH—CH2—CH2-C(O—)NH-Lys-Pr, were M2e is the influenza M2 ectodomain (M2e) peptide; Cys is a cysteine amino acid residue present in the M2e peptide; S the sulfur present in the cysteine amino acid residue; CH2-CO—NH—CH2-CH2-CO the linking group; NH the amine group present in a lysine residue of the carrier; Lys is a lysine amino acid residue and Pr the carrier protein. Also disclosed are isolated immunogens that include an immunogenic fragment of an influenza HA protein including the polybasic cleavage site, wherein the immunogenic fragment of the influenza HA protein has been modified to remove an N-terminal leader amino acid sequence and a C-terminal transmembrane domain. Also disclosed are methods producing an influenza vaccine specific for an identified influenza strain.

    摘要翻译: 公开了具有以下通式的免疫原性缀合物:M2e-Cys-S-CH2-C(O)-NH-CH2-CH2-C(O-NH-Lys-Pr),M2e是流感M2胞外域(M2e)肽 ; Cys是存在于M2e肽中的半胱氨酸氨基酸残基; S存在于半胱氨酸氨基酸残基中的硫; CH2-CO-NH-CH2-CH2-CO连接基团; NH存在于载体的赖氨酸残基中的胺基; Lys是赖氨酸氨基酸残基,Pr是载体蛋白。 还公开了分离的免疫原,其包括包括多碱性切割位点的流感HA蛋白的免疫原性片段,其中已经修饰了流感HA蛋白的免疫原性片段以除去N-末端前导氨基酸序列和C-末端跨膜结构域 。 还公开了产生针对所鉴定的流感病毒株特异的流感疫苗的方法。

    Methods for preparing immunogenic conjugates
    38.
    发明授权
    Methods for preparing immunogenic conjugates 有权
    制备免疫原性缀合物的方法

    公开(公告)号:US08481048B2

    公开(公告)日:2013-07-09

    申请号:US12582420

    申请日:2009-10-20

    摘要: Methods for making an immunogenic conjugate that includes a hapten or an antigen covalently linked to a carrier. The methods include reacting a first agent with a dihydrazide resulting in a hydrazine-modified first agent, wherein the first agent is a hapten, an antigen or a carrier; reacting a second agent with a benzaldehyde compound resulting in a benzaldehyde-modified second agent, wherein the second agent is a hapten, an antigen or a carrier, provided that the first agent or the second agent is a carrier; and reacting the hydrazine-modified first agent with the benzaldehyde-modified second agent resulting in an immunogenic conjugate comprising a hapten or an antigen covalently linked to a carrier via a hydrazone linkage.

    摘要翻译: 制备免疫原性缀合物的方法,其包括与载体共价连接的半抗原或抗原。 所述方法包括使第一试剂与二酰肼反应,得到肼修饰的第一试剂,其中第一试剂是半抗原,抗原或载体; 使第二试剂与苯甲醛化合物反应,得到苯甲醛修饰的第二试剂,其中第二试剂是半抗原,抗原或载体,条件是第一试剂或第二试剂是载体; 并使肼修饰的第一试剂与苯甲醛修饰的第二试剂反应,得到包含通过腙键与载体共价连接的半抗原或抗原的免疫原性缀合物。

    Alignment mark for opaque layer
    39.
    发明授权

    公开(公告)号:US08268696B2

    公开(公告)日:2012-09-18

    申请号:US12964430

    申请日:2010-12-09

    IPC分类号: H01L21/762

    摘要: An IC alignment mark in a contact metal layer for use under an opaque layer, and a process for forming the alignment mark, are disclosed. The alignment mark includes contact metal fields, each several microns wide, with an array of PMD pillars in the interior, formed during contact etch, contact metal deposition and selective contact metal removal processes. The pillars are arrayed such that all exposed surfaces of the contact metal are planar. One configuration is a rectangular array in which every other row is laterally offset by one-half of the column spacing. Horizontal dimensions of the pillars are selected to maximize the contact metal fill factor, while providing sufficient adhesion to the underlying substrate during processing. The contact metal is at least 15 nanometers lower than the PMD layer surrounding the alignment mark, as a result of the contact metal removal process.

    ALIGNMENT MARK FOR OPAQUE LAYER
    40.
    发明申请
    ALIGNMENT MARK FOR OPAQUE LAYER 有权
    OPAQUE层的对齐标记

    公开(公告)号:US20110306176A1

    公开(公告)日:2011-12-15

    申请号:US12964430

    申请日:2010-12-09

    IPC分类号: H01L21/762

    摘要: An IC alignment mark in a contact metal layer for use under an opaque layer, and a process for forming the alignment mark, are disclosed. The alignment mark includes contact metal fields, each several microns wide, with an array of PMD pillars in the interior, formed during contact etch, contact metal deposition and selective contact metal removal processes. The pillars are arrayed such that all exposed surfaces of the contact metal are planar. One configuration is a rectangular array in which every other row is laterally offset by one-half of the column spacing. Horizontal dimensions of the pillars are selected to maximize the contact metal fill factor, while providing sufficient adhesion to the underlying substrate during processing. The contact metal is at least 15 nanometers lower than the PMD layer surrounding the alignment mark, as a result of the contact metal removal process.

    摘要翻译: 公开了在不透明层下使用的接触金属层中的IC对准标记和用于形成对准标记的工艺。 对准标记包括几微米宽的接触金属场,在接触蚀刻,接触金属沉积和选择性接触金属去除过程期间形成在内部的PMD柱阵列。 柱子被排列成使得接触金属的所有暴露表面是平面的。 一个配置是矩形阵列,其中每隔一行被横向偏移列间距的一半。 选择柱的水平尺寸以使接触金属填充因子最大化,同时在处理期间向下面的基底提供足够的粘附。 作为接触金属去除过程的结果,接触金属比围绕对准标记的PMD层低至少15纳米。