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    • 2. 发明申请
    • TREATMENT, DIAGNOSIS AND IMAGING OF DISEASE
    • 疾病的治疗,诊断和成像
    • WO2007101676A2
    • 2007-09-13
    • PCT/EP2007/001962
    • 2007-03-07
    • BIOINVENT INTERNATIONAL ABBORREBAECK, Carl, Arne, KristerEK, Sara
    • BORREBAECK, Carl, Arne, KristerEK, Sara
    • A61K38/17A61K47/6867A61K51/1069C07K16/3061
    • The present invention provides a use a compound comprising a binding moiety which selectively binds to a protein listed in Table 1 in the treatment, imaging, diagnosis or prognosis of mantle cell lymphomas (MCL). Optionally, the compound also comprises a further moiety. Preferably, the binding moiety is an antibody or antigen- binding fragment thereof. Advantageously, the further moiety is a directly or indirectly cytotoxic moiety or a readily detectable moiety. The invention also provides methods of imaging MCL cells, methods of diagnosing or prognosing MCL in an individual and methods of treating an individual with MCL A further aspect of the present invention provides a method of identifying cells associated with MCL, the method comprising analysing the pattern of gene expression in a sample of cells to be tested and comparing it to the pattern of gene expression in a sample of known MCL cells. Preferably, the cells to be tested are identified as MCL cells if the expression of one or more genes encoding a protein listed in Table 1 is upregulated compared to normal B -cells.
    • 本发明提供使用包含结合部分的化合物,所述结合部分选择性地结合表1中列出的蛋白质在外套细胞淋巴瘤(MCL)的治疗,成像,诊断或预后中。 任选地,化合物还包含另外的部分。 优选地,结合部分是抗体或其抗原结合片段。 有利地,另外的部分是直接或间接的细胞毒性部分或易于检测的部分。 本发明还提供了成像MCL细胞的方法,个体中MCL的诊断或预后的方法以及用MCL治疗个体的方法。本发明的另一方面提供了鉴定与MCL相关的细胞的方法,该方法包括分析模式 的基因表达在待测试的细胞样品中,并将其与已知MCL细胞的样品中的基因表达模式进行比较。 如果与正常的B细胞相比,如果编码表1中列出的蛋白质的一种或多种基因的表达上调,则优选将待测试的细胞鉴定为MCL细胞。
    • 3. 发明申请
    • TREATMENT, DIAGNOSIS AND IMAGING OF DISEASE
    • 疾病的治疗,诊断和成像
    • WO2003068268A2
    • 2003-08-21
    • PCT/EP2003/001461
    • 2003-02-13
    • BIOINVENT INTERNATIONAL ABEK, SaraBORREBAECK, Carl, Arne, KristerEHINGER, Mats
    • EK, SaraBORREBAECK, Carl, Arne, KristerEHINGER, Mats
    • A61K51/00
    • A61K47/50
    • The present invention provides the use of a compound comprising: (i) a binding moiety which selectively binds to a protein listed in Table 1 and (ii) a further moiety in the treatment, imaging, diagnosis or prognosis of mantle cell lymphomas (MCL). Preferably, the binding moiety is an antibody or antigenbinding fragment thereof. Advantageously, the further moiety is a directly or indirectly cytotoxic moiety or a readily detectable moiety. The invention also provides methods of imaging MCL cells, methods of diagnosing or prognosing MCL in an individual and methods of treating an individual with MCL. A further aspect of the present invention provides a method of identifying cells associated with MCL, the method comprising analyzing the pattern of gene expression in a sample of cells to be tested and comparing it to the pattern of gene expression in a sample of known MCL cells. Preferably, the cells to be tested are identified as MCL cells if the expression of one or more genes encoding a protein listed in Table 1 is upregulated compared to normal B-cells.
    • 本发明提供了一种化合物的用途,所述化合物包括:选择性结合表1所列蛋白质的结合部分,以及外套细胞淋巴瘤MCL的治疗,成像,诊断或预后的另一部分。 优选地,结合部分是抗体或其抗原结合片段。 有利地,另外的部分是直接或间接的细胞毒性部分或易于检测的部分。 本发明还提供了成像MCL细胞的方法,个体中诊断或预测MCL的方法和用MCL治疗个体的方法。 本发明的另一方面提供了鉴定与MCL相关的细胞的方法,所述方法包括分析待测试细胞样品中基因表达的模式,并将其与已知MCL细胞样品中的基因表达模式进行比较 。 如果与正常B细胞​​相比,如果编码表1中列出的蛋白质的一种或多种基因的表达上调,则优选将待测试的细胞鉴定为MCL细胞。
    • 4. 发明申请
    • METHOD OF DIAGNOSING OR PROGNOSING EPITHELIAL OVARIAN CANCER
    • 诊断或预防上皮癌的方法
    • WO2010023458A1
    • 2010-03-04
    • PCT/GB2009/002098
    • 2009-09-01
    • IMMUNOVIA ABBORREBAECK, Carl, Arne, KristerEK, Sara, Charlotte, AnderssonBRENNAN, Donal, John
    • BORREBAECK, Carl, Arne, KristerEK, Sara, Charlotte, AnderssonBRENNAN, Donal, John
    • C12Q1/68G01N33/574
    • G01N33/57449C12Q1/6886C12Q2600/118C12Q2600/158G01N2500/00G01N2800/56
    • The present invention provides a binding moiety which selectively binds to Sox11 protein and/or mRNA for imaging, diagnosis or prognosis of epithelial ovarian cancer (EOC). Optionally, the moiety is an antibody or antigen-binding fragment thereof. Advantageously, moiety comprises a further, readily detectable moiety. The invention also provides methods of imaging EOC cells as well as methods of diagnosing or prognosing EOC in an individual. A further aspect of the present invention provides a method of identifying cells associated with EOC, the method comprising analysing the pattern of gene expression in a sample of cells to be tested and comparing it to the pattern of gene expression in a sample of known lymphomas cells. Preferably, the cells to be tested are identified as EOC cells if the expression of Sox11 is up-regulated compared to normal B-cells. Preferably EOC cells are identified as improved recurrence-free survival-associated if expression of Sox11 is up-regulated compared with non-cancerous epithelial ovarian cells. Preferably, EOC cells are identified as diminished recurrence-free survival-associated if expression of Sox11 is similar to, or down-regulated, compared with non-cancerous epithelial ovarian cells.
    • 本发明提供了选择性结合Sox11蛋白和/或mRNA用于成像,诊断或预后的上皮性卵巢癌(EOC)的结合部分。 任选地,该部分是抗体或其抗原结合片段。 有利地,部分包含另外易于检测的部分。 本发明还提供对EOC细胞进行成像的方法以及在个体中诊断或预测EOC的方法。 本发明的另一方面提供了鉴定与EOC相关的细胞的方法,所述方法包括分析待测试细胞样品中基因表达的模式,并将其与已知淋巴瘤细胞样品中基因表达的模式进行比较 。 如果与正常B细胞​​相比,如果Sox11的表达被上调,则待测试的细胞被鉴定为EOC细胞。 如果与非癌性上皮性卵巢细胞相比,如果Sox11的表达上调,则优选EOC细胞被鉴定为改善的无复发存活相关性。 优选地,与非癌性上皮性卵巢细胞相比,如果Sox11的表达与非癌性上皮性卵巢细胞相似或下调,则EOC细胞被鉴定为减少的无复发存活相关。
    • 5. 发明申请
    • SOX11 EXPRESSION IN MALIGNANT LYMPHOMAS
    • 恶性淋巴瘤中的SOX11表达
    • WO2008139169A1
    • 2008-11-20
    • PCT/GB2008/001625
    • 2008-05-12
    • IMMUNOVIA ABBORREBAECK, Carl, Arne, KristerEK, Sara
    • BORREBAECK, Carl, Arne, KristerEK, Sara
    • C12Q1/68
    • C12Q1/6886A61K51/1069C07K16/00C07K16/18C12Q2600/118C12Q2600/158G01N33/57496G01N2500/20G01N2800/52
    • The present invention provides a binding moiety which selectively binds to Sox1 1 protein and/or mRNA for imaging, diagnosis or prognosis of lymphomas, such as mantle cell lymphomas (MCL) and diffuse large B-cell lymphoma (DLBCL). Optionally, the moiety is an antibody or antigen-binding fragment thereof. Advantageously, moiety comprises a further, readily detectable moiety. The invention also provides methods of imaging lymphomas cells as well as methods of diagnosing or prognosing lymphomas in an individual. A further aspect of the present invention provides a method of identifying cells associated with lymphomas, the method comprising analysing the pattern of gene expression in a sample of cells to be tested and comparing it to the pattern of gene expression in a sample of known lymphomas cells. Preferably, the cells to be tested are identified as lymphoma cells if the expression of Sox11 is upregulated compared to normal B-cells.
    • 本发明提供了结合部分,其选择性结合Sox1蛋白和/或mRNA用于淋巴瘤(例如外套细胞淋巴瘤(MCL)和弥漫性大B细胞淋巴瘤(DLBCL))的成像,诊断或预后。 任选地,该部分是抗体或其抗原结合片段。 有利地,部分包含另外易于检测的部分。 本发明还提供了对淋巴瘤细胞进行成像的方法以及诊断或预测个体中淋巴瘤的方法。 本发明的另一方面提供了鉴定与淋巴瘤相关的细胞的方法,所述方法包括分析待测试细胞样品中基因表达的模式,并将其与已知淋巴瘤细胞样品中的基因表达模式进行比较 。 如果与正常B细胞​​相比,如果Sox11的表达上调,则优选将待测试的细胞识别为淋巴瘤细胞。
    • 6. 发明申请
    • A METHOD FOR IN VITRO MOLECULAR EVOLUTION OF PROTEIN FUNCTION
    • WO2003097834A3
    • 2003-11-27
    • PCT/GB2003/002102
    • 2003-05-16
    • ALLIGATOR BIOSCIENCE ABTHOMAS, Philip, John, DuvalFUREBRING, ChristinaCARLSSON, RolandBORREBAECK, Carl, Arne, KristerMALMBORG, Hager, Ann-Christin
    • FUREBRING, ChristinaCARLSSON, RolandBORREBAECK, Carl, Arne, KristerMALMBORG, Hager, Ann-Christin
    • C12N15/10
    • A method for in vitro molecular evolution of protein function The invention provides a method for generating a polynucleotide sequence or population of sequences from parent single-stranded polynucleotide sequences encoding one or more protein motifs, comprising the steps of (a) providing a first population of single-stranded polynucleotide molecules and a second population of single-stranded polynucleotide molecules, the first and second populations together constituting plus and minus strands of parent polynucleotide sequences, (b) carrying out a reaction for digesting the first and second populations of single-stranded polynucleotide molecules with an exonuclease to generate corresponding populations of single-stranded polynucleotide fragments, (c) contacting said fragments generated from the plus strands with fragments generated from the minus strands and optionally, adding primer sequences that anneal to the 3'and 5'ends of at least one of the parent polynucleotides under annealing conditions, and (d) amplifying the fragments that anneal to each other to generate at least one polynucleotide sequence encoding one or more protein motifs having altered characteristics as compared to the one or more protein motifs encoded by said parent polynucleotides, wherein, in step (b), at least one parameter of the reaction used for digestion of the first population of single-stranded polynucleotide molecules is different from the equivalent parameter(s) used in the reaction for digestion of the second population of single-stranded polynucleotide molecules. Preferably, the reaction parameter is selected from exonuclease type, exonuclease concentration, reaction volume, duration of the digestion reaction, temperature of the reaction mixture, pH of the reaction mixture, length of parent single­-stranded polynucleotide sequences, amount of single-stranded polynucleotide molecules and buffer composition of the reaction mixture.