ANTIBODIES FOR DIAGNOSIS AND THERAPEUTIC TREATMENT OF PROSTATE CANCER
    3.
    发明申请
    ANTIBODIES FOR DIAGNOSIS AND THERAPEUTIC TREATMENT OF PROSTATE CANCER 审中-公开
    用于诊断和治疗前列腺癌的抗体

    公开(公告)号:US20110206695A1

    公开(公告)日:2011-08-25

    申请号:US13013002

    申请日:2011-01-25

    IPC分类号: A61K39/395 C12Q1/70 A61P35/00

    摘要: XMRV appears to be related to both prostate cancer if it infects a male germ cell and chronic fatigue syndrome in both sexes. (If the virus does not infect a germ cell). Prostate cancer cells exhibit TSG101 on the surface only upon infection with a virus like XMRV. Antibodies to TSG101 can be effective diagnostics to identify individuals with a predisposition to prostate. They can also be used in place of current diagnostics to confirm the presence of prostate cancer. TSG101 antibodies, when administered in vivo, exhibit the ability to reduce tumor size, suppress metastatic transformation and extend survival.

    摘要翻译: XMRV似乎与前列腺癌相关,如果它感染男性生殖细胞和慢性疲劳综合征两性。 (如果病毒不感染生殖细胞)。 前列腺癌细胞只有在感染了像XMRV这样的病毒时才在表面上显示TSG101。 对TSG101的抗体可以有效地诊断以鉴别具有前列腺炎倾向的个体。 它们也可以用于代替目前的诊断以确认前列腺癌的存在。 TSG101抗体在体内施用时,具有减少肿瘤大小,抑制转移转化和延长存活的能力。

    Methods of inhibiting viral infection
    7.
    发明授权
    Methods of inhibiting viral infection 失效
    抑制病毒感染的方法

    公开(公告)号:US08207209B2

    公开(公告)日:2012-06-26

    申请号:US12256571

    申请日:2008-10-23

    IPC分类号: A61K31/4184

    摘要: A method of inhibiting viral respiratory infection in a mammal in need of same, includes administering an effective amount of 2-[2-(5-carbamimidoyl-benzofuran-2-yl)-vinyl]-H-benzoimidazole-5-carboxamidine or the Bis-N-hydroxyamidine prodrug thereof, prior to viral infection, or therapeutically following viral infection, to inhibit that viral infection. The compound selectively inhibits Caspase 2 and/or 8 as to prevent infective viral particle release. It is optionally administered IV, IP, orally or via other conventional administration routes in a dosage range of 1 ng/kg-200 mg/kg of body weight.

    摘要翻译: 在需要相同的哺乳动物中抑制病毒呼吸道感染的方法包括给予有效量的2- [2-(5-甲脒基 - 苯并呋喃-2-基) - 乙烯基] -H-苯并咪唑-5-甲脒或 双-N-羟基脒前药,在病毒感染之前,或治疗性地在病毒感染之后,以抑制该病毒感染。 该化合物选择性地抑制胱天蛋白酶2和/或8以防止感染性病毒颗粒释放。 任选地以1ng / kg-200mg / kg体重的剂量范围以IV,IP口服或经由其它常规给药途径施用。

    Random homozygous gene perturbation to enhance antibody production
    8.
    发明授权
    Random homozygous gene perturbation to enhance antibody production 有权
    随机纯合基因扰动以增强抗体产生

    公开(公告)号:US07745148B2

    公开(公告)日:2010-06-29

    申请号:US11928393

    申请日:2007-10-30

    IPC分类号: G01N33/53

    CPC分类号: C07K16/00

    摘要: The invention reflects enhanced antibody expression of an antibody of interest by cell lines transformed by random homozygous gene perturbation methods to either increase or decrease the expression pattern of a gene of the cell line other than the antibody of interest. The transformed cell line exhibits specific productivity rates, SPR, for the RHGP transformed cell liens of 1.5 or more, as compared with the antibody expressing cell line parents prior to transformation by RHGP. A knock out or anti-sense construct may be devised to reduce expression of the target gene, a promoter may be inserter to enhance expression of the target gene. The antibodies expressed by the transformed cell lines exhibit the binding properties of their parent cell lines prior to transformation with RHGP, and increase Total Volumetric Production of said antibody by said cells in a given volume.

    摘要翻译: 本发明反映了通过随机纯合基因扰动方法转化的细胞系增强或减少除感兴趣抗体之外的细胞系的基因的表达模式的目标抗体的增强的抗体表达。 与通过RHGP转化之前与抗体表达细胞系亲本相比,转化细胞系表现出1.5GP以上RHGP转化细胞留置量的比生产率SPR。 可以设计敲除或反义构建体以减少靶基因的表达,启动子可以被插入以增强靶基因的表达。 由转化的细胞系表达的抗体在用RHGP转化之前表现出其亲本细胞系的结合特性,并且增加所述细胞在给定体积中的所述抗体的总体积产量。

    METHOHDS OF INHIBITING VIRAL INFECTION
    10.
    发明申请
    METHOHDS OF INHIBITING VIRAL INFECTION 失效
    抑制病毒感染的甲基化

    公开(公告)号:US20090170890A1

    公开(公告)日:2009-07-02

    申请号:US12256571

    申请日:2008-10-23

    IPC分类号: A61K31/4745 A61P31/12

    摘要: A method of inhibiting viral infection in a mammal in need of same, includes administering an effective amount of at least one of the compounds of FGI-103 which are represented by 273, 365 and 510 either prophylactically to prevent viral infection, or therapeutically following viral infection. These compounds appear to selectively inhibit Caspase 8 as a method of preventing infective viral particle release. They can be administered IV, IP, orally or via other conventional administration routes. The compounds are highly effective, requiring relatively low dosages on the order of 1 ng/kg-200 mg/kg of body weight.

    摘要翻译: 在需要相同的哺乳动物中抑制病毒感染的方法包括以预防方式施用有效量的至少一种由273,355和510表示的FGI-103化合物,以预防病毒感染或治疗性病毒感染 感染。 这些化合物似乎选择性地抑制胱天蛋白酶8作为预防感染性病毒颗粒释放的方法。 它们可以IV,IP,口服或其他常规给药途径给药。 这些化合物是非常有效的,需要相当低的剂量约1ng / kg-200mg / kg体重。