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    • 1. 发明申请
    • METHOD FOR PREPARING MESO-2,3-BUTANEDIOL
    • 制备MESO-2,3-丁醇的方法
    • WO2012124890A2
    • 2012-09-20
    • PCT/KR2012000436
    • 2012-01-18
    • UNIV SOGANG IND UNIV COOP FOUNLEE JIN WONLEE SOO JINKIM BO-RIMCHOI WOO JOO
    • LEE JIN WONLEE SOO JINKIM BO-RIMCHOI WOO JOO
    • C12N1/21C12N15/53C12N15/60C12N15/70C12P7/16
    • C12P7/16C12N9/0006C12N9/88C12Y101/01001C12Y101/01004C12Y401/01005Y02E50/10
    • The present invention relates to a method for preparing meso-2,3-butanediol. More particularly, the present invention relates to colon bacillus for overexpressing meso-2,3-butaediol, which is cotransformed to an expression vector including at least one nucleotide SEQ ID selected from the group consisting of the following nucleotide SEQ IDs: (a) nucleotide-coding acetoin reductase having an amino acid sequence described in SEQ ID 5 of a sequence listing; (b) nucleotide-coding acetolactate decarboxylase; and (c) nucleotide-coding alcohol dehydrogenase. The cotransformed colon bacillus of the present invention can produce 2,3-butanediol, which could not be obtained from wild species. Therefore, it is possible to biosynthesize a large amount of meso-2,3-butanediol through the biosynthesis path expression of meso-2,3-butanediol from glucose, and through metabolic flux change by means of the insertion of the genes of other species.
    • 本发明涉及一种制备内消旋-2,3-丁二醇的方法。 更具体地,本发明涉及用于过表达内切-2,3-丁二醇的大肠杆菌,其被共转化成包含至少一个选自以下核苷酸SEQ ID的核苷酸SEQ ID的核苷酸SEQ ID:(a)核苷酸 - 具有序列表的SEQ ID 5所示的氨基酸序列的乙偶姻还原酶; (b)核苷酸编码乙酰乳酸脱羧酶; 和(c)核苷酸编码的醇脱氢酶。 本发明的共转化大肠杆菌可以产生不能从野生种获得的2,3-丁二醇。 因此,可以通过葡萄糖的内消旋-2,3-丁二醇的生物合成途径表达生物合成大量的内消旋-2,3-丁二醇,通过其他物种的基因插入代谢通量变化是可能的 。
    • 7. 发明申请
    • NOVEL COMBINATIONS FOR ANTIGEN BASED THERAPY
    • 基于抗原治疗的新型组合
    • WO2015187087A3
    • 2016-01-28
    • PCT/SE2015050651
    • 2015-06-04
    • DIAMYD MEDICAL AB
    • ESSEN-MÖLLER ANDERSLUDVIGSSON JOHNNY
    • A61K39/00A61K31/592A61K31/593A61K38/28A61P3/10
    • A61K39/0008A61K9/0019A61K31/192A61K31/197A61K31/592A61K31/593A61K38/1793A61K38/191A61K38/28A61K38/43A61K45/06A61K2039/54A61K2039/55505A61K2039/577C12Y401/01005A61K2300/00
    • The present invention relates to a method for prevention and/or treatment of an autoimmune disease, comprising administering a composition, said composition comprising at least one beta cell autoantigen, to a subject The subject may have a serum vitamin-D level above 50 nanomole/liter or the composition may be administered by intralymphatic injection or injection directly into a lymph node, or over a period of weeks, months, or years. The invention also relates to a composition comprising a plurality of particles, each having immobilised on its surface at least one first and at least one second antigen, wherein the first antigen is a beta cell autoantigen, and the second antigen is either a tolerogen or a beta cell autoantigen, andto composition comprising i) at least one beta cell autoantigen, and at least one of iia) an IL-10 inducing compound selected from the group consisting of vitamin-D, vitamin-D analogs, tyrosine kinase inhibitors, gamma-amino butyric acid, and gamma-amino butyric acid analogs; and iib) a compound that reduces the dendritic cells' ability to activate naïve CD4+ Tcells, such as a cyclooxygenase inhibitor, a CTLA-4 compound or a TNF alpha inhibitor. The invention also relates to pharmaceutical kits and to medical use of beta cell autoantigens.
    • 本发明涉及一种预防和/或治疗自身免疫性疾病的方法,包括向受试者施用包含至少一种β细胞自身抗原的所述组合物。所述受试者可具有高于50纳摩尔/ 或者组合物可以通过淋巴内注射或直接注射到淋巴结中,或在数周,数月或数年的时间内施用。 本发明还涉及包含多个颗粒的组合物,每个颗粒在其表面上固定有至少一个第一和至少一个第二抗原,其中第一抗原是β细胞自身抗原,第二抗原是耐受原或 β细胞自身抗原,以及组合物,其包含i)至少一种β细胞自身抗原,和iia中的至少一种,IL-10诱导化合物,其选自维生素D,维生素-D类似物,酪氨酸激酶抑制剂, 氨基丁酸和γ-氨基丁酸类似物; 和iib)降低树突状细胞激活初始CD4 + T细胞的能力的化合物,例如环氧合酶抑制剂,CTLA-4化合物或TNFα抑制剂。 本发明还涉及药物试剂盒和β细胞自身抗原的医疗用途。
    • 8. 发明申请
    • NOVEL COMBINATIONS FOR ANTIGEN BASED THERAPY
    • 基于抗原治疗的新型组合
    • WO2015187087A2
    • 2015-12-10
    • PCT/SE2015/050651
    • 2015-06-04
    • DIAMYD MEDICAL AB
    • ESSEN-MÖLLER, AndersLUDVIGSSON, Johnny
    • A61K39/00
    • A61K39/0008A61K9/0019A61K31/192A61K31/197A61K31/592A61K31/593A61K38/1793A61K38/191A61K38/28A61K38/43A61K45/06A61K2039/54A61K2039/55505A61K2039/577C12Y401/01005A61K2300/00
    • The present invention relates to a method for prevention and/or treatment of an autoimmune disease, comprising administering a composition, said composition comprising at least one beta cell autoantigen, to a subject The subject may have a serum vitamin-D level above 50 nanomole/liter or the composition may be administered by intralymphatic injection or injection directly into a lymph node, or over a period of weeks, months, or years. The invention also relates to a composition comprising a plurality of particles, each having immobilised on its surface at least one first and at least one second antigen, wherein the first antigen is a beta cell autoantigen, and the second antigen is either a tolerogen or a beta cell autoantigen, andto composition comprising i) at least one beta cell autoantigen, and at least one of iia) an IL-10 inducing compound selected from the group consisting of vitamin-D, vitamin-D analogs, tyrosine kinase inhibitors, gamma-amino butyric acid, and gamma-amino butyric acid analogs; and iib) a compound that reduces the dendritic cells' ability to activate naïve CD4+ Tcells, such as a cyclooxygenase inhibitor, a CTLA-4 compound or a TNF alpha inhibitor. The invention also relates to pharmaceutical kits and to medical use of beta cell autoantigens.
    • 本发明涉及一种预防和/或治疗自身免疫性疾病的方法,包括向受试者施用包含至少一种β细胞自身抗原的所述组合物。所述受试者可具有高于50纳摩尔/ 或者组合物可以通过淋巴内注射或直接注射到淋巴结中,或在数周,数月或数年的时间内施用。 本发明还涉及包含多个颗粒的组合物,每个颗粒在其表面上固定有至少一个第一和至少一个第二抗原,其中第一抗原是β细胞自身抗原,第二抗原是耐受原或 β细胞自身抗原,以及组合物,其包含i)至少一种β细胞自身抗原,和iia中的至少一种,IL-10诱导化合物,其选自维生素D,维生素-D类似物,酪氨酸激酶抑制剂, 氨基丁酸和γ-氨基丁酸类似物; 和iib)降低树突状细胞激活初始CD4 + T细胞的能力的化合物,例如环氧合酶抑制剂,CTLA-4化合物或TNFα抑制剂。 本发明还涉及药物试剂盒和β细胞自身抗原的医疗用途。