METHODS OF TREATING TUMORS IN IMMUNE-PRIVILEGED SITES
    12.
    发明申请
    METHODS OF TREATING TUMORS IN IMMUNE-PRIVILEGED SITES 有权
    在免疫特异性位点治疗肿瘤的方法

    公开(公告)号:US20100189750A1

    公开(公告)日:2010-07-29

    申请号:US12677543

    申请日:2008-09-11

    CPC classification number: A61K39/0011 A61K2039/5152

    Abstract: A method of treating cancer in an immune-privileged site of a subject in need thereof is provided. The method comprises systemically administering to an area outside the immune-privileged site of the subject, a therapeutically effective amount of naive, viable cells of a tumor of the subject, the tumor being in the immune-privileged site so as to generate an immune response in the subject, thereby treating the cancer in the immune-privileged site of the subject.

    Abstract translation: 提供了在有需要的受试者的免疫特异部位中治疗癌症的方法。 该方法包括系统地施用受试者的免疫特权部位之外的区域,治疗有效量的受试者肿瘤的天真,活的细胞,肿瘤位于免疫特异位点以产生免疫应答 从而治疗受试者的免疫特异部位的癌症。

    Allogeneic cell therapy for cancer following allogeneic stem cell
transplantation
    13.
    发明授权
    Allogeneic cell therapy for cancer following allogeneic stem cell transplantation 失效
    同种异体干细胞移植后的同种异体细胞治疗癌症

    公开(公告)号:US06143292A

    公开(公告)日:2000-11-07

    申请号:US930071

    申请日:1997-11-21

    Applicant: Shimon Slavin

    Inventor: Shimon Slavin

    CPC classification number: A61K38/2013 A61K35/17

    Abstract: A method of treating a human cancer patient having a solid tumor comprising malignant cells is disclosed, wherein the patient having undergone a cancer therapy regimen comprising allogeneic stem cell transplantation. The method comprises administering allogeneic lymphocytes to the patient and monitoring the patient for levels of malignant cells.

    Abstract translation: PCT No.PCT / US96 / 07652 Sec。 371日期:1997年11月21日 102(e)1997年11月21日PCT PCT 1996年5月24日PCT公布。 WO96 / 37208 PCT公开号 日本1996年11月28日公开了一种治疗患有包含恶性细胞的实体肿瘤的人类癌症患者的方法,其中已经经过包括同种异体干细胞移植的癌症治疗方案的患者。 该方法包括向患者施用同种异体淋巴细胞并监测患者恶性细胞的水平。

    Quinazolinone-containing pharmaceutical compositions and methods for the
use thereof
    14.
    发明授权
    Quinazolinone-containing pharmaceutical compositions and methods for the use thereof 失效
    含喹唑啉酮的药物组合物及其使用方法

    公开(公告)号:US5891879A

    公开(公告)日:1999-04-06

    申请号:US722046

    申请日:1996-12-09

    CPC classification number: A61K31/517

    Abstract: The invention provides a pharmaceutical composition for preventing restens by the inhibition of vascular smooth muscle cell proliferation, comprising a compound of formula I: ##STR1## wherein: n=1 or 2 R.sub.1 is a member of the group consisting of hydrogen, halogen, nitro, benzo, lower alkyl, phenyl and lower alkoxy;R.sub.2 is a member of the group consisting of hydroxy, acetoxy, and lower alkoxy, andR.sub.3 is a member of the group consisting of hydrogen and lower alkenoxy-carbonylas active ingredient therein, and the physiologically acceptable salts thereof, in combination with a pharmaceutically acceptable carrier.

    Abstract translation: PCT No.PCT / US95 / 11186 Sec。 371日期1996年12月9日第 102(e)日期1996年12月9日PCT提交1995年8月29日PCT公布。 出版物WO96 / 06616 日期:1996年3月7日本发明提供了一种用于通过抑制血管平滑肌细胞增殖来预防再狭窄的药物组合物,其包含式I化合物:其中:n = 1或2 R 1为下列成员: 的氢,卤素,硝基,苯并,低级烷基,苯基和低级烷氧基; R2是由羟基,乙酰氧基和低级烷氧基组成的组的成员,R3是作为其中作为活性成分的氢和低级链烯氧基 - 羰基的成员,其生理上可接受的盐与药学上可接受的盐组合 可接受的载体

    Use of quinoline-3-carboxamide compounds for treatment of diabetes
    15.
    发明授权
    Use of quinoline-3-carboxamide compounds for treatment of diabetes 失效
    使用喹啉-3-甲酰胺化合物治疗糖尿病

    公开(公告)号:US5594005A

    公开(公告)日:1997-01-14

    申请号:US313302

    申请日:1994-12-23

    Abstract: Quinoline-3-carboxamide compounds of formula (I) are effective in preventing, treating or ameliorating Type I diabetes. ##STR1## wherein ----- represents two conjugated double bonds between the atoms comprised by the dashed line, X.sub.1 and X.sub.2 are independently selected from an oxygen atom or NH.sup.9, H.sup.1-9 independently represent a hydrogen atom or a substituent, wherein H.sup.7 and H.sup.8 are attached to different atoms selected from X.sub.1, X.sub.2 and the ring nitrogen atom of the quinoline ring. In particular, X.sub.1 and X.sub.2 being bound by a single bond to the ring when H.sup.7 or H.sup.8 is bonded thereto and by a double bond when H.sup.7 or H.sup.8 is not bonded thereto.

    Abstract translation: PCT No.PCT / SE93 / 00272 Sec。 371日期1994年12月23日第 102(e)日期1994年12月23日PCT 1993年3月31日PCT公布。 WO93 / 19756 PCT公开号 日期:1993年10月14日式(I)的喹啉-3-甲酰胺化合物可有效预防,治疗或改善I型糖尿病。 其中-----表示由虚线包含的原子之间的两个共轭双键,X1和X2独立地选自氧原子或NH9,H1-9独立地表示氢原子或取代基,其中H7 和H8连接到选自X1,X2和喹啉环的环氮原子的不同原子。 特别地,当H 7或H 8键合时,X 1和X 2通过单键与环结合,当H7或H8未键合时,X 1和X 2与双键结合。

    Methods, systems, and compositions for neuronal differentiation of multipotent stromal cells

    公开(公告)号:US10421961B2

    公开(公告)日:2019-09-24

    申请号:US13377558

    申请日:2010-06-10

    Abstract: Some embodiments of the invention comprise methods, systems, and compositions to selectively induce, whether in vitro or in vivo, the neuronal differentiation of multipotent stromal cells through the application of microRNAs, including but not limited to miRNA-124, miRNA-137 and/or miRNA-9* expression products of those miRNAs, and molecules and compositions containing functional elements of those miRNAs. Some embodiments of the invention also comprise the therapeutic administration and use of such induced cells to treat mammalian injuries and diseases, including but not limited to, nervous system injuries or diseases that may otherwise result in decreased cell or system function.

    METHODS OF GENERATING OLIGODENDROCYTES AND CELL POPULATIONS COMPRISING SAME
    17.
    发明申请
    METHODS OF GENERATING OLIGODENDROCYTES AND CELL POPULATIONS COMPRISING SAME 有权
    产生含有寡糖的小鼠和细胞群体的方法

    公开(公告)号:US20130149288A1

    公开(公告)日:2013-06-13

    申请号:US13817535

    申请日:2011-08-14

    Abstract: A method of generating a population of cells useful for treating a brain disorder in a subject is disclosed. The method comprises contacting mesenchymal stem cells (MSCs) with at least one exogenous miRNA having a nucleic acid sequence at least 90% identical to a sequence selected from the group consisting of SEQ ID NOs: 15-19 and 27-35, thereby generating the population of cells and/or generating neurotrophic factors that may provide important signals to damaged tissues or locally residing stem cells. MSCs differentiated by miRs may also secrete miRs and deliver them to adjacent cells and therefore provide important signals to neighboring endogenous normal or malignant cells.

    Abstract translation: 公开了一种产生可用于治疗受试者脑部疾病的细胞群的方法。 所述方法包括使间充质干细胞(MSC)与至少一种外源miRNA接触,所述外源miRNA具有与选自SEQ ID NO:15-19和27-35的序列至少90%相同的核酸序列,从而产生 细胞群和/或产生神经营养因子,其可以向受损组织或局部驻留的干细胞提供重要信号。 通过miR分化的MSC也可以分泌miR并将其递送至相邻细胞,并因此向相邻内源性正常或恶性细胞提供重要信号。

    SYNTHETIC SPHINGOLIPID ANALOGS
    18.
    发明申请
    SYNTHETIC SPHINGOLIPID ANALOGS 审中-公开
    合成弹性体类似物

    公开(公告)号:US20100311841A1

    公开(公告)日:2010-12-09

    申请号:US12742036

    申请日:2008-11-06

    CPC classification number: C07C323/32 C07C381/12

    Abstract: Therapeutic compounds based on synthetic sphingolipid analogs are provided, particularly alkylthiophenyl substituted ceramide analogs, suitable for treating degenerative, infectious, and other diseases.

    Abstract translation: 提供了基于合成鞘脂类似物的治疗化合物,特别是烷基硫代苯基取代的神经酰胺类似物,其适于治疗退行性,感染性和其它疾病。

    Methods of treatment of hematopoietic disorders
    19.
    发明授权
    Methods of treatment of hematopoietic disorders 有权
    造血障碍治疗方法

    公开(公告)号:US07347999B2

    公开(公告)日:2008-03-25

    申请号:US10471048

    申请日:2002-03-05

    CPC classification number: A61K35/32 A61K35/28 A61K38/1875 A61K2300/00

    Abstract: A composition comprising bone marrow cells (BMC) and demineralized bone matrix (DBM) and/or mineralized bone matrix (MBM), optionally comprising bone morphogenetic protein (BMP), particularly for use in bone marrow transplantation, into bone marrow cavity or into extraskeletal sites, and methods of transplantation/implantation thereof. The composition and methods of the invention enable restoring and/or enhancing the formation of hematopoiectic microenvironment originating from the transplanted BMC, and are useful in the treatment of hematopoietic disorders, such as deficiency of stem cells and/or their products, genetic conditions resulting in abnormal stem cells and/or products, or hematopoietic disorders of malignant or non-malignant origin. The composition and method of the invention may also be used for the induction of graft tolerence, for the prevention of graft-v-host disease. It is mostly important that the compositions and methods of the invention may be applied for the treatment of diseases affecting primarily or secondarily the stromal microenvironment that supports and regulates hematopoiesis. Further provided is a kit for transplantation into a mammal of BMC in admixture with DBM and/or MBM.

    Abstract translation: 包含骨髓细胞(BMC)和去矿物质骨基质(DBM)和/或矿化骨基质(MBM)的组合物,任选地包括骨形态发生蛋白(BMP),特别是用于骨髓移植,进入骨髓腔或骨骼外 位点及其移植/植入方法。 本发明的组合物和方法能够恢复和/或增强源自移植的BMC的造血微环境的形成,并且可用于治疗造血障碍,例如干细胞和/或其产物的缺乏,导致 异常干细胞和/或产物,或恶性或非恶性起源的造血障碍。 本发明的组合物和方法也可用于诱导移植物穿刺,用于预防移植物抗宿主病。 最重要的是,本发明的组合物和方法可以用于治疗主要或二次影响支持和调节造血的基质微环境的疾病。 还提供了用于与DBM和/或MBM混合的用于移植到BMC的哺乳动物中的试剂盒。

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