会员体验
专利管家(专利管理)
工作空间(专利管理)
风险监控(情报监控)
数据分析(专利分析)
侵权分析(诉讼无效)
联系我们
交流群
官方交流:
QQ群: 891211   
微信请扫码    >>>
现在联系顾问~
热词
    • 2. 发明申请
    • Anti-interferon alpha monoclonal antibodies and methods for use
    • 抗干扰素α单克隆抗体及其使用方法
    • US20140154239A1
    • 2014-06-05
    • US13705289
    • 2012-12-05
    • Jacques BanchereauKiley PrillimanVirginia PascualAnna Karolina Palucka
    • Jacques BanchereauKiley PrillimanVirginia PascualAnna Karolina Palucka
    • C07K16/24
    • C07K16/249C07K2317/24C07K2317/33C07K2317/565C07K2317/76C07K2317/92
    • The present invention includes compositions and methods that include antibodies that selectively neutralize a bioactivity of at least two interferon alpha (“IFNα”) protein subtypes for the protein subtypes A, 2, B2, C, F, G, H2, I, J1, K, 4a, 4b and WA, but does not neutralize at least one bioactivity of IFNα protein subtype D. Examples of bioactivity for measurement include activation of the MxA promoter or antiviral activity and variants, derivatives and fragments thereof. The invention also includes host cells, hybridomas and plasmacytomas that produce antibodies. Because of their unique selectivity and affinity, the antibodies of the present invention are useful to detect IFNα subtypes in sample or tissue and/or for therapeutic applications that include, but are not limited to the treatment and/or amelioration of an IFNα related disorder such as SLE, lupus, type I diabetes, psoriasis, AIDS and Graft versus Host Disease.
    • 本发明包括组合物和方法,其包括选择性中和至少两种干扰素α(“IFNα”)蛋白亚型对于蛋白质亚型A,2,B2,C,F,G,H2,I,J1的生物活性的抗体, K,4a,4b和WA,但不中和IFNα蛋白亚型D的至少一种生物活性。用于测量的生物活性的实例包括MxA启动子的活化或抗病毒活性及其变体,衍生物和片段。 本发明还包括产生抗体的宿主细胞,杂交瘤和浆细胞瘤。 由于其独特的选择性和亲和性,本发明的抗体可用于检测样品或组织和/或治疗应用中的IFNα亚型,包括但不限于IFNα相关病症的治疗和/或改善,例如 如SLE,狼疮,I型糖尿病,牛皮癣,艾滋病和移植物抗宿主病。
    • 9. 发明申请
    • Rapid one-step generation of antigen loaded dendritic cell vaccine from precursors
    • 从前体快速一步生成抗原负载的树突状细胞疫苗
    • US20060239962A1
    • 2006-10-26
    • US10537682
    • 2003-12-04
    • Jacques BANCHEREAU
    • Jacques BANCHEREAU
    • A61K39/00A61K9/127A61K38/19
    • A61K39/0011A61K2039/5152A61K2039/5154C12N5/0639C12N2501/22C12N2501/25
    • A one-step method for producing antigen loaded antigen-presenting cells from monocytes ex vivo has been found which comprises contacting the monocytes with a composition comprising an activator such as TNF alpha preferably in combination with at least one growth factor such as GM-CSF and at least one soluble or particulate antigen. According to the methods of the present invention, antigen-loaded dendritic cell vaccines can be generated within as little as three (3) days. In another method of the present invention, antigen loaded antigen-presenting cells are produced from monocytes ex vivo by contacting the monocytes with TNF alpha and granulocyte-macrophage colony stimulating factor at one time point to form antigen-presenting cells and then contacting antigen-presenting cells with soluble or particulate antigenic material antigen-presenting cells, wherein the antigen loaded antigen-presenting cells are produced in less than four days. The present invention also includes a vaccine which comprises monocyte-derived antigen loaded antigen-presenting cells, wherein the antigenpresenting cells are composed of two or more subsets selected from the group consisting of Langerhans cells with surface markers (CD 1 a+CD207+); interstitial dendritic cells with surface markers (CD 1a+CD207−); double negative dendritic cells with surface markers 20 (CD 1 a−CD 14−); and dendritic cells with surface markers (CD 14+CD 1 a−CD209+).
    • 已经发现从体外从单核细胞产生抗原负载抗原呈递细胞的一步法包括使单核细胞与包含活化剂如TNFα的组合物接触,优选与至少一种生长因子如GM-CSF和 至少一种可溶或微粒抗原。 根据本发明的方法,可以在短短三(3)天内产生抗原负载的树突状细胞疫苗。 在本发明的另一种方法中,抗原呈递细胞由单核细胞通过单核细胞与TNFα和粒细胞 - 巨噬细胞集落刺激因子在一个时间点接触形成抗原呈递细胞,然后使抗原呈递细胞接触 具有可溶性或微粒抗原性材料抗原呈递细胞的细胞,其中抗原呈递细胞的抗原呈递细胞在不到四天的时间内产生。 本发明还包括一种疫苗,其包含单核细胞衍生的抗原负载抗原呈递细胞,其中所述抗原呈递细胞由两个或更多个选自具有表面标记的朗格汉斯细胞(CD1a + CD207 +)的子集组成; 具有表面标志物的间质树突状细胞(CD 1a + CD207-); 具有表面标记20的双负性树突状细胞(CD 1 a-CD 14-); 和具有表面标志物(CD14 + CD1a-CD209 +)的树突状细胞。
    • 10. 发明授权
    • Anti-inteferon alpha monoclonal antibodies and methods for use
    • 抗全蛋白α单克隆抗体及其使用方法
    • US08333965B2
    • 2012-12-18
    • US13252335
    • 2011-10-04
    • Jacques BanchereauKiley PrillimanVirginia PascualAnna Karolina Palucka
    • Jacques BanchereauKiley PrillimanVirginia PascualAnna Karolina Palucka
    • A61K39/395A61K38/00C07K16/00C12P21/08
    • C07K16/249A61K2039/505C07K2317/24C07K2317/76
    • The present invention includes compositions and methods that include antibodies that selectively neutralize a bioactivity of at least two interferon alpha (“IFNα”) protein subtypes for the protein subtypes A, 2, B2, C, F, G, H2, I, J1, K, 4a, 4b and WA, but does not neutralize at least one bioactivity of IFNα protein subtype D. Examples of bioactivity for measurement include activation of the MxA promoter or antiviral activity and variants, derivatives and fragments thereof. The invention also includes host cells, hybridomas and plasmacytomas that produce antibodies. Because of their unique selectivity and affinity, the antibodies of the present invention are useful to detect IFNα subtypes in sample or tissue and/or for therapeutic applications that include, but are not limited to the treatment and/or amelioration of an IFNα related disorder such as SLE, lupus, type I diabetes, psoriasis, AIDS and Graft versus Host Disease.
    • 本发明包括组合物和方法,其包括选择性中和至少两种干扰素α(IFNα)蛋白亚型对于蛋白质亚型A,2,B2,C,F,G,H2,I,J1,K的生物活性的抗体, 4a,4b和WA,但不中和IFNα蛋白亚型D的至少一种生物活性。用于测量的生物活性的实例包括MxA启动子的活化或抗病毒活性及其变体,衍生物和片段。 本发明还包括产生抗体的宿主细胞,杂交瘤和浆细胞瘤。 由于其独特的选择性和亲和性,本发明的抗体可用于检测样品或组织和/或治疗应用中的IFNα亚型,包括但不限于IFNα相关病症的治疗和/或改善,例如 如SLE,狼疮,I型糖尿病,牛皮癣,艾滋病和移植物抗宿主病。