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    • 4. 发明申请
    • Treatment of systemic lupus erythematosus by down-regulating the autoimmune response to autoantigens
    • 通过下调对自身抗原的自身免疫反应来治疗系统性红斑狼疮
    • US20060030524A1
    • 2006-02-09
    • US11179820
    • 2005-07-13
    • Irun CohenVarda RotterNeta ErezJohannes Herkel
    • Irun CohenVarda RotterNeta ErezJohannes Herkel
    • A61K48/00A61K38/17
    • C07K14/4746A61K38/00A61K39/00A61K2039/505C07K16/18C07K16/4241G01N33/564G01N2800/104
    • Systemic lupus erythematosus (SLE) can be prevented or treated by down-regulating the autoimmune response to the C-terminal-DNA-binding domain of the p53 protein (p53) by an active principle selected from the group consisting of: (i) a peptide of, or comprising, the C-terminal DNA-binding domain of the p53 protein; (ii) a monoclonal antibody (mAb) specific for said domain of p53 (Ab1), and fragments thereof; (iii) an mAb specific for Ab1 (hereinafter Ab2), and fragments thereof; (iv) a peptide based on a complementarity determining region (CDR) of the heavy or light chain of said Ab1 or Ab2; (v) a DNA molecule coding for (i) and (iv) of for the variable region of said Ab1 and Ab2 of (ii) and (iii); and (vi) T cells specific for (i) to (iv), fragments thereof, T cell receptor (TCR) thereof and peptides comprising the variable region of said TCR. SLE can also be diagnosed by assaying for antibodies (Ab1) against the C-terminal DNA-binding domain of p53 or antibodies (Ab2) specific to the Ab1 antibodies.
    • 可以通过选自以下的活性成分下调对自身免疫应答p53蛋白(p53)的C末端-DNA结合结构域的自身免疫应答来防止或治疗系统性红斑狼疮(SLE):(i) 或包含p53蛋白的C-末端DNA结合结构域的肽; (ii)对所述p53结构域(Ab1)特异的单克隆抗体(mAb)及其片段; (iii)Ab1(以下称Ab2)特异性的mAb及其片段; (iv)基于所述Ab1或Ab2的重链或轻链的互补决定区(CDR)的肽; (v)编码(i)和(iv)的(ii)和(iii)所述Ab1和Ab2的可变区的DNA分子; 和(vi)特异于(i)至(iv)的T细胞,其片段,T细胞受体(TCR)和包含所述TCR的可变区的肽。 也可以通过测定针对p53的C末端DNA结合结构域的抗体(Ab1)或Ab1抗体特异性抗体(Ab2)来诊断SLE。
    • 10. 发明申请
    • Antigen Receptor Variable Region Typing
    • 抗原受体可变区域键入
    • US20070238099A1
    • 2007-10-11
    • US10581913
    • 2004-10-25
    • Irun CohenDaniel DouekAvishai MimranPnina CarmiFrancisco Quintana
    • Irun CohenDaniel DouekAvishai MimranPnina CarmiFrancisco Quintana
    • C12Q1/68C07H21/02C07H21/04C12M1/00
    • C12Q1/6883C07K14/7051C12Q1/6876C12Q2600/156
    • A method of typing a variable region of a specific variant of an antigen receptor chain is disclosed. The method comprises: (a) exposing a probe set to a sense or antisense strand of a polynucleotide encoding at least a portion of the variable region of the specific variant of the antigen receptor chain, wherein the probe set includes a plurality of probe molecules, wherein each probe molecule of the plurality of probe molecules is substantially complementary to a sense or antisense strand of a nucleic acid sequence region of a specific polynucleotide encoding a variant of the antigen receptor chain, the nucleic acid sequence region encoding a specific combination of at least two variable region segments of the antigen receptor chain; and (b) measuring a hybridization of each probe molecule of the plurality of probe molecules with the sense or antisense strand of the nucleic acid sequence region of the polynucleotide encoding at least a portion of the variable region of the specific variant of the antigen receptor chain, thereby typing the variable region of the specific variant of the antigen receptor chain.
    • 公开了一种对抗原受体链的特定变体的可变区进行分型的方法。 该方法包括:(a)将探针组暴露于编码抗原受体链特异性变体的至少一部分可变区的多核苷酸的有义或反义链,其中探针组包括多个探针分子, 其中所述多个探针分子中的每个探针分子基本上与编码抗原受体链变体的特异性多核苷酸的核酸序列区域的有义链或反义链互补,所述核酸序列区编码至少 抗原受体链的两个可变区片段; 和(b)测量多个探针分子的每个探针分子与编码抗原受体链特异变体的可变区的至少一部分的核酸序列区的有义链或反义链的杂交 ,从而键入抗原受体链的特定变体的可变区。