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    • 1. 发明申请
    • PRE-TRANSPLANT IgG REACTIVITY TO APOPTOTIC CELLS CORRELATES WITH LATE KIDNEY ALLOGRAFT LOSS
    • PRE-TRANSPLANT对具有最近的KIDNEY ALLOGRAFT LOSS的相关细胞的IgG反应性
    • US20150219667A1
    • 2015-08-06
    • US14614998
    • 2015-02-05
    • Emmanuel Zorn
    • Emmanuel Zorn
    • G01N33/68A61M1/34
    • G01N33/6854A61M2202/0021A61M2202/0417G01N2510/00G01N2800/245G01N2800/50
    • It has been discovered that significantly elevated levels of anti-apoptotic cell IgG is an important contributor to and predictor of late graft rejection. Kaplan-Meier survival analysis revealed that patients with high pre-transplant IgG and post-transplant reactivity to apoptotic cells had a significantly increased rate of late graft loss that was apparent after approximately 1 year post-transplant. This association between pre-transplant IgG reactivity to apoptotic cells and graft loss was still significant after excluding patients with high reactivity to HLA, and it was almost exclusively mediated by IgG1 and IgG3 with complement fixing and activating properties. The association between elevated levels of anti-apoptotic cell IgG antibodies and late transplant rejection forms a basis for diagnosing and treating patients at high risk of late transplant rejection.
    • 已经发现,抗凋亡细胞IgG水平显着升高是晚期移植排斥反应的重要贡献和预测因子。 Kaplan-Meier生存分析显示,移植前高IgG和移植后对凋亡细胞的反应性的患者在移植后大约1年后明显增加晚期移植物丢失率。 排除移植后IgG对细胞凋亡的反应和移植物损失之间的关联在排除HLA高反应性的患者后仍然显着,并且几乎完全由具有补体固定和活化性质的IgG1和IgG3介导。 抗凋亡细胞IgG抗体水平升高与晚期移植排斥反应之间的联系形成诊断和治疗晚期移植排斥高风险患者的基础。
    • 2. 发明授权
    • Method and compositions for treatments of cancers
    • 治疗癌症的方法和组合物
    • US06231536B1
    • 2001-05-15
    • US09316226
    • 1999-05-21
    • M. Rigdon Lentz
    • M. Rigdon Lentz
    • A61M3700
    • A61K35/14A61K31/00A61K31/337A61K31/454A61K31/555A61K31/704A61K35/16A61K38/18A61K38/1816A61K38/193A61K38/196A61K41/00A61K41/0019A61M1/34A61M1/342A61M1/3441A61M1/3472A61M1/3482A61M1/3681A61M2202/0417A61M2205/50A61M2205/75A61N5/1028B01D15/00B01D29/50B01D37/00B01D61/02A61K2300/00
    • A method to treat cancer uses ultrapheresis, refined to remove compounds of less than 120,000 daltons molecular weight, followed by administration of replacement fluid, to stimulate the patient's immune system to attack solid tumors. In the preferred embodiment, the patient is ultrapheresed using a capillary tube ultrafilter having a pore size of 0.02 to 0.05 microns, with a molecular weight cutoff of 120,000 daltons, sufficient to filter one blood volume. The preferred replacement fluid is ultrapheresed normal plasma. The patient is preferably treated daily for three weeks, diagnostic tests conducted to verify that there has been shrinkage of the tumors, then the treatment regime is repeated. The treatment is preferably combined with an alternative therapy, for example, treatment with an anti-angiogenic compound, one or more cytokines such as TNF, gamma interferon, or IL-2, or a procoagulant compound. The treatment increases endogenous, local levels of cytokines, such as TNF. This provides a basis for an improved effect when combined with any treatment that enhances cytokine activity against the tumors, for example, treatments using alkylating agents, doxyrubicin, carboplatinum, cisplatinum, and taxol. Alternatively, the ultrapheresis treatment can be combined with local chemotherapy, systemic chemotherapy, and/or radiation.
    • 一种治疗癌症的方法是使用超级血液分离法,精制以除去小于120,000道尔顿分子量的化合物,然后施用替代液,以刺激患者的免疫系统攻击实体瘤。 在优选实施例中,使用孔径为0.02至0.05微米,分子量截留值为120,000道尔顿的毛细管超滤器将患者超薄,足以过滤一个血液体积。 优选的替代液体是超分离的正常血浆。 患者优选每天治疗三周,进行诊断测试以证实肿瘤已经收缩,然后重复治疗方案。 治疗优选与替代疗法组合,例如用抗血管生成化合物,一种或多种细胞因子如TNF,γ干扰素或IL-2或促凝血剂化合物的治疗。 治疗增加内源性,局部水平的细胞因子,如TNF。 当提供增强细胞因子对肿瘤活性的治疗,例如使用烷化剂,多柔比星,卡铂,顺铂和紫杉醇的治疗时,这提供了改善效果的基础。 或者,超单位治疗可以与局部化疗,全身化学疗法和/或辐射结合。
    • 5. 发明申请
    • METHOD AND COMPOSITIONS FOR TREATMENT OF CANCERS
    • 用于治疗癌症的方法和组合物
    • US20150231178A1
    • 2015-08-20
    • US14498605
    • 2014-09-26
    • M. Rigdon Lentz
    • M. Rigdon Lentz
    • A61K35/14A61N5/10A61M1/36A61K35/16A61K31/454
    • A61K35/14A61K31/00A61K31/337A61K31/454A61K31/555A61K31/704A61K35/16A61K38/18A61K38/1816A61K38/193A61K38/196A61K41/00A61K41/0019A61M1/34A61M1/342A61M1/3441A61M1/3472A61M1/3482A61M1/3603A61M1/3681A61M2202/0417A61M2205/50A61M2205/75A61N5/10A61N5/1028B01D15/00B01D29/50B01D37/00B01D61/02A61K2300/00
    • A method to treat cancer uses ultrapheresis, refined to remove compounds of less than 120,000 daltons molecular weight, followed by administration of replacement fluid, to stimulate the patient's immune system to attack solid tumors. In the preferred embodiment, the patient is ultrapheresed using a capillary tube ultrafilter having a pore size of 0.02 to 0.05 microns, with a molecular weight cutoff of 120,000 daltons, sufficient to filter one blood volume. The preferred replacement fluid is ultrapheresed normal plasma. The patient is preferably treated daily for three weeks, diagnostic tests conducted to verify that there has been shrinkage of the tumors, then the treatment regime is repeated. The treatment is preferably combined with an alternative therapy, for example, treatment with an anti-angiogenic compound, one or more cytokines such as TNF, gamma interferon, or IL-2, or a procoagulant compound. The treatment increases endogenous, local levels of cytokines, such as TNF. This provides a basis for an improved effect when combined with any treatment that enhances cytokine activity against the tumors, for example, treatments using alkylating agents, doxyrubicin, carboplatinum, cisplatinum, and taxol. Alternatively, the ultrapheresis treatment can be combined with local chemotherapy, systemic chemotherapy, and/or radiation.
    • 一种治疗癌症的方法是使用超级血液分离法,精制以除去小于120,000道尔顿分子量的化合物,然后施用替代液,以刺激患者的免疫系统攻击实体瘤。 在优选实施例中,使用孔径为0.02至0.05微米,分子量截留值为120,000道尔顿的毛细管超滤器将患者超薄,足以过滤一个血液体积。 优选的替代液体是超分离的正常血浆。 患者优选每天治疗三周,进行诊断测试以证实肿瘤已经收缩,然后重复治疗方案。 治疗优选与替代疗法组合,例如用抗血管生成化合物,一种或多种细胞因子如TNF,γ干扰素或IL-2或促凝血剂化合物的治疗。 治疗增加内源性,局部水平的细胞因子,如TNF。 当提供增强细胞因子对肿瘤活性的治疗,例如使用烷化剂,多柔比星,卡铂,顺铂和紫杉醇的治疗时,这提供了改善效果的基础。 或者,超单位治疗可以与局部化疗,全身化学疗法和/或辐射结合。