ANTI-C (EPSILON)MX ANTIBODIES CAPABLE OF BINDING TO HUMAN MIGE ON B LYMPHOCYTES
    1.
    发明申请
    ANTI-C (EPSILON)MX ANTIBODIES CAPABLE OF BINDING TO HUMAN MIGE ON B LYMPHOCYTES 有权
    抗体(EPSILON)MX抗体可以绑定到B淋巴细胞上的人类

    公开(公告)号:US20140220042A1

    公开(公告)日:2014-08-07

    申请号:US14254453

    申请日:2014-04-16

    Abstract: The invention pertains to the generation and utility of antibodies that can bind effectively to CεmX domain on membrane-bound IgE (mIgE) expressed on the surface of human B lymphocytes. The CεmX domain of 52 amino acid residues, located between the CH4 domain and the C-terminal membrane-anchor peptide on human membrane-bound epsilon chain, had been suggested as an antigenic site for immunological targeting of B cells expressing mIgE. Previous reported monoclonal antibodies, including a20, which bind to RADWPGPP (SEQ ID NO:1) peptide at the C-terminal of CεmX, have now been found to bind poorly to mIgE on human B cells. We have discovered that only monoclonal antibodies specific for certain segments, such as GLAGGSAQSQRAPDRVL (SEQ ID NO:2) and HSGQQQGLPRAAGGSVPHPR (SEQ ID NO:3), of CεmX can bind effectively to mIgE on human B cells and hence have the utility for targeting those B cells for the treatment of diseases mediated by IgE.

    Abstract translation: 本发明涉及能够在人B淋巴细胞表面表达的膜结合IgE(mIgE)上有效结合C& mX结构域的抗体的产生和应用。 已经提出位于人膜结合的ε链上的CH4结构域和C末端膜锚定肽之间的52个氨基酸残基的Cys区域作为用于免疫靶向表达mIgE的B细胞的抗原位点。 目前已经发现,以前报道的,在C细胞C末端结合RADWPGPP(SEQ ID NO:1)肽的单克隆抗体,包括a20,现在已被发现与人B细胞上的mIgE结合不良。 我们已经发现,对于某些片段(例如GLAGGSAQSQRAPDRVL(SEQ ID NO:2)和HSGQQQGLPRAAGGSVPHPR(SEQ ID NO:3))特异性的单克隆抗体,C& mX可以有效地结合到人B细胞上的mIgE,因此具有效用 用于靶向这些B细胞用于治疗由IgE介导的疾病。

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