Compositions and methods for cancer immunotherapy
    1.
    发明授权
    Compositions and methods for cancer immunotherapy 有权
    癌症免疫治疗的组成和方法

    公开(公告)号:US08795672B2

    公开(公告)日:2014-08-05

    申请号:US10779267

    申请日:2004-02-13

    IPC分类号: A61K39/395

    摘要: Provided is a cancer therapeutic agent comprising a cancer targeting molecule linked to a liver-expressed chemokine (LEC). In one embodiment, the cancer targeting molecule is an antibody that targets cancer cells or tumors in vivo. The cancer targeting molecule is associated non-covalently or covalently with LEC. The cancer therapeutic agents of the invention are useful for the treatment of cancer in an individual by reducing the size of a tumor or inhibiting the growth of cancer cells in an individual and/or by inhibiting the development of metastasis. The effectiveness of the therapy using the LEC cancer therapeutic agents can be increased by reducing the activity of immunoregulatory T cells and/or by adoptively transferring immune T cells.

    摘要翻译: 提供了包含与肝表达趋化因子(LEC)连接的癌靶向分子的癌症治疗剂。 在一个实施方案中,癌靶向分子是在体内靶向癌细胞或肿瘤的抗体。 癌症靶向分子与LEC非共价或共价相关。 本发明的癌症治疗剂可用于通过减少肿瘤的大小或抑制个体中癌细胞的生长和/或通过抑制转移的发展来治疗个体中的癌症。 可以通过降低免疫调节性T细胞的活性和/或通过过继转移免疫T细胞来增加使用LEC癌症治疗剂的治疗的有效性。

    COMPOSITIONS AND METHODS FOR CANCER IMMUNOTHERAPY
    2.
    发明申请
    COMPOSITIONS AND METHODS FOR CANCER IMMUNOTHERAPY 审中-公开
    癌症免疫组织和方法

    公开(公告)号:US20140099305A1

    公开(公告)日:2014-04-10

    申请号:US13865902

    申请日:2013-04-18

    IPC分类号: A61K47/48 A61K38/19

    摘要: Provided is a cancer therapeutic agent comprising a cancer targeting molecule linked to a liver-expressed chemokine (LEC). In one embodiment, the cancer targeting molecule is an antibody that targets cancer cells or tumors in vivo. The cancer targeting molecule is associated non-covalently or covalently with LEC. The cancer therapeutic agents of the invention are useful for the treatment of cancer in an individual by reducing the size of a tumor or inhibiting the growth of cancer cells in an individual and/or by inhibiting the development of metastasis. The effectiveness of the therapy using the LEC cancer therapeutic agents can be increased by reducing the activity of immunoregulatory T cells and/or by adoptively transferring immune T cells.

    摘要翻译: 提供了包含与肝表达趋化因子(LEC)连接的癌靶向分子的癌症治疗剂。 在一个实施方案中,癌靶向分子是在体内靶向癌细胞或肿瘤的抗体。 癌症靶向分子与LEC非共价或共价相关。 本发明的癌症治疗剂可用于通过减少肿瘤的大小或抑制个体中癌细胞的生长和/或通过抑制转移的发展来治疗个体中的癌症。 可以通过降低免疫调节性T细胞的活性和/或通过过继转移免疫T细胞来增加使用LEC癌症治疗剂的治疗的有效性。

    Compositions and methods for cancer immunotherapy
    3.
    发明授权
    Compositions and methods for cancer immunotherapy 有权
    癌症免疫治疗的组成和方法

    公开(公告)号:US08545838B2

    公开(公告)日:2013-10-01

    申请号:US11674569

    申请日:2007-02-13

    IPC分类号: A61K39/395

    摘要: Provided is a cancer therapeutic agent comprising a cancer targeting molecule linked to a liver-expressed chemokine (LEC). In one embodiment, the cancer targeting molecule is an antibody that targets cancer cells or tumors in vivo. The cancer targeting molecule is associated non-covalently or covalently with LEC. The cancer therapeutic agents of the invention are useful for the treatment of cancer in an individual by reducing the size of a tumor or inhibiting the growth of cancer cells in an individual and/or by inhibiting the development of metastasis. The effectiveness of the therapy using the LEC cancer therapeutic agents can be increased by reducing the activity of immunoregulatory T cells and/or by adoptively transferring immune T cells.

    摘要翻译: 提供了包含与肝表达趋化因子(LEC)连接的癌靶向分子的癌症治疗剂。 在一个实施方案中,癌靶向分子是在体内靶向癌细胞或肿瘤的抗体。 癌症靶向分子与LEC非共价或共价相关。 本发明的癌症治疗剂可用于通过减少肿瘤的大小或抑制个体中癌细胞的生长和/或通过抑制转移的发展来治疗个体中的癌症。 可以通过降低免疫调节性T细胞的活性和/或通过过继转移免疫T细胞来增加使用LEC癌症治疗剂的治疗的有效性。

    Therapeutic use of interleukin-2 mutants
    4.
    发明授权
    Therapeutic use of interleukin-2 mutants 有权
    白介素-2突变体的治疗用途

    公开(公告)号:US07514073B2

    公开(公告)日:2009-04-07

    申请号:US11093073

    申请日:2005-03-29

    IPC分类号: A61K38/20

    摘要: Interleukin-2 (IL-2) mutants having reduced toxicity, which include full-length IL-2, truncated forms of IL-2 and forms of IL-2 that are linked to another molecule are disclosed herein. Particular substitutions within IL-2, particularly within the permeability enhancing peptide region of IL-2 achieve substantial reduction of vasopermeability activity as compared to a wildytpe form of the mutant IL-2 while retaining many of the immune activating properties of IL-2. Invention IL-2 mutants can be used to stimulate the immune system of an animal and may be used in the treatment of various disorders and conditions.

    摘要翻译: 本文公开了具有降低的毒性的白细胞介素-2(IL-2)突变体,其包括全长IL-2,截短形式的IL-2和与另一分子连接的IL-2形式。 与IL-2的野生型相比,IL-2中特别是IL-2的通透性增强肽区域内的特异性置换可以显着降低血管通透性活性,同时保留IL-2的许多免疫激活特性。 本发明的IL-2突变体可用于刺激动物的免疫系统并且可用于治疗各种疾病和病症。

    THERAPEUTIC USE OF INTERLEUKIN-2 MUTANTS
    5.
    发明申请
    THERAPEUTIC USE OF INTERLEUKIN-2 MUTANTS 有权
    白介素-2突变体的治疗应用

    公开(公告)号:US20110091413A1

    公开(公告)日:2011-04-21

    申请号:US12888315

    申请日:2010-09-22

    摘要: Interleukin-2 (IL-2) mutants having reduced toxicity, which include full-length IL-2, truncated forms of IL-2 and forms of IL-2 that are linked to another molecule are disclosed herein. Particular substitutions within IL-2, particularly within the permeability enhancing peptide region of IL-2 achieve substantial reduction of vasopermeability activity as compared to a wildytpe form of the mutant IL-2 while retaining many of the immune activating properties of IL-2. Invention IL-2 mutants can be used to stimulate the immune system of an animal and may be used in the treatment of various disorders and conditions.

    摘要翻译: 本文公开了具有降低的毒性的白细胞介素-2(IL-2)突变体,其包括全长IL-2,截短形式的IL-2和与另一分子连接的IL-2形式。 与IL-2的野生型相比,IL-2中特别是IL-2的通透性增强肽区域内的特异性置换可以显着降低血管通透性活性,同时保留IL-2的许多免疫激活特性。 本发明的IL-2突变体可用于刺激动物的免疫系统并且可用于治疗各种疾病和病症。

    INTERLEUKIN-2 MUTANTS WITH REDUCED TOXICITY
    6.
    发明申请
    INTERLEUKIN-2 MUTANTS WITH REDUCED TOXICITY 有权
    具有降低毒性的白细胞介素-2突变体

    公开(公告)号:US20090274653A1

    公开(公告)日:2009-11-05

    申请号:US12419960

    申请日:2009-04-07

    IPC分类号: A61K38/20

    摘要: Interleukin-2 (IL-2) mutants having reduced toxicity, which include full-length IL-2, truncated forms of IL-2 and forms of IL-2 that are linked to another molecule are disclosed herein. Particular substitutions within IL-2, particularly within the permeability enhancing peptide region of IL-2 achieve substantial reduction of vasopermeability activity as compared to a wildytpe form of the mutant IL-2 while retaining many of the immune activating properties of IL-2. Invention IL-2 mutants can be used to stimulate the immune system of an animal and may be used in the treatment of various disorders and conditions.

    摘要翻译: 本文公开了具有降低的毒性的白细胞介素-2(IL-2)突变体,其包括全长IL-2,截短形式的IL-2和与另一分子连接的IL-2形式。 与IL-2的野生型相比,IL-2中特别是IL-2的通透性增强肽区域内的特异性置换可以显着降低血管通透性活性,同时保留IL-2的许多免疫激活特性。 本发明的IL-2突变体可用于刺激动物的免疫系统并且可用于治疗各种疾病和病症。

    Interleukin-2 mutants with reduced toxicity
    7.
    发明授权
    Interleukin-2 mutants with reduced toxicity 有权
    白细胞介素-2突变体毒性降低

    公开(公告)号:US07371371B2

    公开(公告)日:2008-05-13

    申请号:US10218197

    申请日:2002-08-12

    IPC分类号: A61K38/20 C07K14/55

    摘要: Interleukin-2 (IL-2) mutants having reduced toxicity, which include full-length IL-2, truncated forms of IL-2 and forms of IL-2 that are linked to another molecule are disclosed herein. Particular substitutions within IL-2, particularly within the permeability enhancing peptide region of IL-2 achieve substantial reduction of vasopermeability activity as compared to a wildtype form of the mutant IL-2 while retaining many of the immune activating properties of IL-2. Invention IL-2 mutants can be used to stimulate the immune system of an animal and may be used in the treatment of various disorders and conditions.

    摘要翻译: 本文公开了具有降低的毒性的白细胞介素-2(IL-2)突变体,其包括全长IL-2,截短形式的IL-2和与另一分子连接的IL-2形式。 与IL-2的野生型形式相比,IL-2特别是IL-2的通透性增强肽区域内的特异性置换可以显着降低血管通透性活性,同时保留IL-2的许多免疫激活特性。 本发明的IL-2突变体可用于刺激动物的免疫系统并且可用于治疗各种疾病和病症。

    OX40L fusion protein for the immunotherapy of tumors of veterinary animals

    公开(公告)号:US10196435B2

    公开(公告)日:2019-02-05

    申请号:US14543714

    申请日:2014-11-17

    摘要: Provided is an isolated recombinant polypeptide comprising an immunoglobulin domain and a canine OX40L extracellular domain polypeptide fragment or a biological equivalent thereof and compositions comprising: an isolated recombinant polypeptide comprising an immunoglobulin domain and a canine OX40L extracellular domain polypeptide fragment; and a pharmaceutically acceptable carrier. Also provided are methods for treating or ameliorating the symptoms of cancer in a canine comprising administering an effective amount of the isolated recombinant polypeptide of the disclosure and/or a composition of the disclosure to a canine in need thereof.

    Methods of using interleukin-2 mutants with reduced toxicity
    10.
    发明授权
    Methods of using interleukin-2 mutants with reduced toxicity 有权
    使用毒性降低的白细胞介素-2突变体的方法

    公开(公告)号:US08124066B2

    公开(公告)日:2012-02-28

    申请号:US12888315

    申请日:2010-09-22

    IPC分类号: A61K38/20

    摘要: Interleukin-2 (IL-2) mutants having reduced toxicity, which include full-length IL-2, truncated forms of IL-2 and forms of IL-2 that are linked to another molecule are disclosed herein. Particular substitutions within IL-2, particularly within the permeability enhancing peptide region of IL-2 achieve substantial reduction of vasopermeability activity as compared to a wildtype form of the mutant IL-2 while retaining many of the immune activating properties of IL-2. Invention IL-2 mutants can be used to stimulate the immune system of an animal and may be used in the treatment of various disorders and conditions.

    摘要翻译: 本文公开了具有降低的毒性的白细胞介素-2(IL-2)突变体,其包括全长IL-2,截短形式的IL-2和与另一分子连接的IL-2形式。 与IL-2的野生型形式相比,IL-2特别是IL-2的通透性增强肽区域内的特异性置换可以显着降低血管通透性活性,同时保留IL-2的许多免疫激活特性。 本发明的IL-2突变体可用于刺激动物的免疫系统并且可用于治疗各种疾病和病症。