Peptides and pharmaceutical compositions comprising them
    71.
    发明授权
    Peptides and pharmaceutical compositions comprising them 失效
    包含它们的肽和药物组合物

    公开(公告)号:US06096314A

    公开(公告)日:2000-08-01

    申请号:US817177

    申请日:1997-06-30

    摘要: The present invention relates generally to peptide sequences, and method of their use, which sequences modulate the activity of anti-idiotypic T cells. The activity of the anti-idiotypic T cells of interest is related to the ability of these T cells to recognize anti-p277 T cells. The peptides of the present invention thus include important tools in the effort to diagnose, prevent, alleviate or treat disease related to insulin-dependent diabetes mellitus (IDDM).

    摘要翻译: PCT No.PCT / US95 / 12686 Sec。 371日期:1997年6月20日 102(e)日期1996年6月20日PCT提交1995年10月10日PCT公布。 公开号WO96 / 11214 PCT 日期1996年04月18日本发明一般涉及肽序列及其使用方法,该序列调节抗独特型T细胞的活性。 感兴趣的抗独特型T细胞的活性与这些T细胞识别抗p277T细胞的能力有关。 因此,本发明的肽包括用于诊断,预防,缓解或治疗与胰岛素依赖性糖尿病(IDDM)有关的疾病的重要工具。

    Compositions and methods for regulation of active TNF-.alpha.
    72.
    发明授权
    Compositions and methods for regulation of active TNF-.alpha. 失效
    用于调节活性TNF-α的组合物和方法

    公开(公告)号:US6020323A

    公开(公告)日:2000-02-01

    申请号:US486127

    申请日:1995-06-07

    摘要: Substances comprising disaccharides and substances comprising carboxylated and/or sulfated oligosaccharides in substantially purified form, and methods of using same, are disclosed for the regulation of cytokine activity in a host. For instance, the secretion of active Tumor Necrosis Factor Alpha (TNF-.alpha.) can be either inhibited or augmented selectively by administration to the host of an effective amount of a substance of the invention. Thus, the present invention also relates to pharmaceutical compositions and their use for the prevention and/or treatment of pathological processes involving the induction of active cytokine secretion, such as TNF-.alpha.. The invention also relates to the initiation of a desirable immune system-related response by the host to the presence of activators, including pathogens. The substances and pharmaceutical compositions of the present invention may be administered daily, at very low effective doses, typically below 0.1 mg/kg human, or at intervals of up to about 5-8 days, preferably once a week.

    摘要翻译: 公开了包含二糖的物质和包含基本纯化形式的羧化和/或硫酸化寡糖的物质及其使用方法,用于调节宿主中的细胞因子活性。 例如,活性肿瘤坏死因子α(TNF-α)的分泌可以通过给予宿主有效量的本发明的物质而被选择性地抑制或增强。 因此,本发明还涉及药物组合物及其用于预防和/或治疗涉及诱导活性细胞因子分泌的病理过程如TNF-α的用途。 本发明还涉及由宿主引起包括病原体在内的活化剂的存在引起所需的免疫系统相关应答。 本发明的物质和药物组合物可以以非常低的有效剂量(通常低于0.1mg / kg的人)或以至多约5-8天,优选每周一次的间隔施用。

    Method of reducing the severity of host vs graft reaction by
down-regulating hsp60 autoimmunity
    73.
    发明授权
    Method of reducing the severity of host vs graft reaction by down-regulating hsp60 autoimmunity 失效
    通过下调hsp60自身免疫降低宿主与移植物反应的严重程度的方法

    公开(公告)号:US5993803A

    公开(公告)日:1999-11-30

    申请号:US706209

    申请日:1996-08-30

    CPC分类号: A61K38/1709 G01N33/505

    摘要: A method for reducing the severity of host vs graft reaction (HVGR) by the transplant recipient of donor organ or tissue by the transplant recipient and is based on the discovery that hsp60 autoimmunity can function as an accelerator of foreign immunity and the down-regulation of hsp60 autoimmunity suppresses or prevents the graft rejection reaction. Administration of any composition which causes the down-regulation of hsp60 autoimmunity, such as hsp60 or peptide p277 in a tolerogenic carrier or a biologically active carrier capable of mediating a TH1.fwdarw.TH2 shift, will thus reduce the severity of HVGR.

    摘要翻译: 一种通过移植受体的供体器官或组织的移植受体降低宿主对移植物反应(HVGR)的严重性的方法,并且基于这样的发现,即hsp60自身免疫可以作为外源免疫的加速剂和下调 hsp60自身免疫抑制或阻止移植排斥反应。 导致导致hsp60自身免疫性下调的任何组合物,例如能够介导TH1-> TH2转移的耐受性载体或生物活性载体中的hsp60或肽p277将因此降低HVGR的严重性。

    Method for decreasing tumor metastasis
    75.
    发明授权
    Method for decreasing tumor metastasis 失效
    减少肿瘤转移的方法

    公开(公告)号:US4882318A

    公开(公告)日:1989-11-21

    申请号:US67582

    申请日:1987-06-24

    CPC分类号: A61K31/715

    摘要: The invention relates to pharmaceutical compositions intended to decrease the incidence of tumor metastasis in patients who suffer from malignant diseases.The pharmaceutical compositions of the invention contain as active ingredient heparin or a suitable derivative thereof. Amongst suitable derivatives are N-desulfated and N-acetylated heparin.The dosage of the administered heparin or heparin derivative is quite critical and will generally be in the range of from 0.05 mg/kg/day to about 0.5 mg/kg/day. A preferred range is between about 0.1 mg/kg/day to about 0.5 mg/kg/day.

    摘要翻译: 本发明涉及旨在降低患有恶性疾病的患者的肿瘤转移发生率的药物组合物。 本发明的药物组合物含有作为活性成分的肝素或其合适的衍生物。 其中合适的衍生物是N-脱硫和N-乙酰化肝素。 给药的肝素或肝素衍生物的剂量是非常关键的,通常在0.05mg / kg /天至约0.5mg / kg /天的范围内。 优选的范围为约0.1mg / kg /天至约0.5mg / kg /天。