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    • 21. 发明申请
    • ESTROGEN MODULATION OF IFN-GAMMA-MEDIATED CONDITIONS AND DISEASES
    • IFN-GAMMA介导的病症和疾病的雌激素调节
    • WO2005115469A2
    • 2005-12-08
    • PCT/US2005/018161
    • 2005-05-24
    • CEDARS-SINAI MEDICAL CENTERGONSKY, RivkahTARGAN, Stephan, R.
    • GONSKY, RivkahTARGAN, Stephan, R.
    • A61K45/00
    • A61K31/56A61K35/26Y02A50/481
    • Particular aspects provide methods for: modulating IFN-γ-mediated conditions and diseases ( e.g. inflammation, HIV/AIDS, etc). Additionally provided are methods for: reducing IFN-γ expression or secretion in cultured mammalian cells, comprising culturing in the presence of at least one agent selected from the group consisting of estrogen, estriol, estrone and a SERM; for ex-vivo therapy for an IFN-γ-mediated condition or disease, comprising culturing isolated lymphoid cells in the presence of at least one of the above agents; for treating an IFN-γ-mediated condition or disease in a mammal, comprising administering to a subject at least one at least one of the above agents; for treating an IFN-γ-mediated condition or disorder in a gender-dependent manner; for conferring estrogen-responsive expression using a recombinant SNP IFN-γ-179G/T promoter; and for gene therapy using same. Preferably, mammalian cells are human, selected from T cells, PBL, LPMC, and combinations thereof. In particular aspects, the cells are female.
    • 具体方面提供了用于调节IFN-γ介导的病症和疾病(例如炎症,HIV / AIDS等)的方法。 另外提供了用于:减少培养的哺乳动物细胞中的IFN-γ表达或分泌的方法,包括在至少一种选自雌激素,雌三醇,雌酮和SERM的药剂的存在下培养; 用于IFN-γ介导的病症或疾病的离体治疗,包括在至少一种上述试剂存在下培养分离的淋巴样细胞; 用于治疗哺乳动物中的IFN-γ介导的病症或疾病,包括向受试者施用至少一种上述药物中的至少一种; 用于以性别依赖的方式治疗IFN-γ介导的病症或障碍; 用于使用重组SNP IFN-γ-179G / T启动子赋予雌激素反应性表达; 并使用相同的基因治疗。 优选地,哺乳动物细胞是人,选自T细胞,PBL,LPMC及其组合。 在特定方面,细胞是雌性的。
    • 27. 发明申请
    • DIAGNOSIS, PREVENTION AND TREATMENT OF ULCERATIVE COLITIS, AND CLINICAL SUBTYPES THEREOF, USING HISTONE H1
    • 诊断,预防和治疗精神分裂症及其临床亚型,使用HISTONE H1
    • WO1997038713A1
    • 1997-10-23
    • PCT/US1997006987
    • 1997-04-11
    • THE REGENTS OF THE UNIVERSITY OF CALIFORNIACEDARS-SINAI MEDICAL CENTER
    • THE REGENTS OF THE UNIVERSITY OF CALIFORNIACEDARS-SINAI MEDICAL CENTERBRAUN, JonathanTARGAN, Stephan, R.EGGENA, Mark
    • A61K39/00
    • G01N33/564A61K39/0008
    • The present invention provides a method of diagnosing ulcerative colitis (UC) in a subject suspected of having inflammatory bowel disease by obtaining a sample from the individual; contacting the sample with human histone H1, or pANCA-reactive fragment thereof, under conditions suitable to form a complex of human histone H1, or pANCA-reactive fragment thereof, and antibody to human histone H1; and detecting the presence or absence of the complex, where the presence of the complex indicates that the individual has UC. The invention also provides related methods of diagnosing a perinuclear anti-neutrophil cytoplasmic antibody positive (pANCA-positive) clinical subtype of UC in a patient with UC. In addition, the invention further provides methods of determining susceptibility to UC in an individual. The invention further provides methods of inducing tolerance in a pANCA-positive patient with UC by administering an effective dose of histone H1, or tolerogenic fragment thereof, to the pANCA-positive patient with UC. Compositions of histone H1, or fragment thereof, combined with a tolerogizing molecule also are provided.
    • 本发明提供一种通过从个体获得样品来诊断疑似患有炎症性肠病的受试者的溃疡性结肠炎(UC)的方法; 在适于形成人组蛋白H1或其pANCA反应性片段的复合物和人组蛋白H1的抗体的条件下,将样品与人组蛋白H1或其pANCA反应性片段接触; 并检测复合物的存在或不存在,其中复合物的存在表明个体具有UC。 本发明还提供了在UC患者中诊断UC的核周抗中性粒细胞胞质抗体阳性(pANCA阳性)临床亚型的相关方法。 此外,本发明还提供了确定个体对UC的易感性的方法。 本发明进一步提供了通过向具有UC的pANCA阳性患者施用有效剂量的组蛋白H1或其耐受性片段来诱导具有UC的pANCA阳性患者的耐受性的方法。 还提供组蛋白H1或其片段的组合物与耐受性分子组合。
    • 28. 发明申请
    • METHODS OF DETERMINING THE RISK OF POUCHITIS DEVELOPMENT
    • 确定发展风险的方法
    • WO1997038642A1
    • 1997-10-23
    • PCT/US1997005583
    • 1997-04-03
    • CEDARS-SINAI MEDICAL CENTER
    • CEDARS-SINAI MEDICAL CENTERTARGAN, Stephan, R.FLESCHNER, PhillipPLEVY, Scott, E.
    • A61B19/00
    • G01N33/6893G01N33/56972G01N2800/065
    • The present invention provides a method of determining a risk of pouchitis development following a surgical procedure whereby colon is removed and an internal pouch is created in a patient with UC by determining a first pANCA titer, where the first pANCA titer is determined following the surgical procedure; determining a second pANCA titer at a later time; and comparing the first pANCA titer and the second pANCA titer, where a significantly elevated second pANCA titer indicates an increased risk of pouchitis development. In addition, the invention provides a method of determining a risk of pouchitis development following a surgical procedure whereby colon is removed and an internal pouch is created in a patient with UC by determining a first pANCA titer, where the first pANCA titer is determined prior to the surgical procedure; determining a second pANCA titer following said surgical procedure; and comparing the first pANCA titer and the second pANCA titer, where a significantly elevated second pANCA titer indicates an increased risk of pouchitis development.
    • 本发明提供一种在外科手术之后确定囊泡炎发展的风险的方法,其中结肠被移除,并且通过确定第一pANCA滴度在患有UC的患者中产生内部小袋,其中在手术过程之后确定第一pANCA滴度 ; 在稍后时间确定第二个pANCA滴度; 并比较第一个pANCA滴度和第二个pANCA滴度,其中明显升高的第二个pANCA滴度表明发生囊泡炎的风险增加。 另外,本发明提供了一种确定外科手术后肠粘膜炎发展风险的方法,其中结肠被移除并且通过确定第一pANCA滴度来确定第一pANCA滴度,在患有UC的患者中产生内部小袋,其中第一pANCA滴度在 外科手术; 在所述外科手术之后确定第二pANCA滴度; 并比较第一个pANCA滴度和第二个pANCA滴度,其中明显升高的第二个pANCA滴度表明发生囊泡炎的风险增加。