Anti-c (epsilon)mx antibodies capable of binding to human mige on b lymphocytes
AssigneeAcademia Sinica
InventorsTse Wen Chang, Jiun-Bo Chen, Pheidias C. Wu, Alfur F. Hung
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AssigneeAcademia Sinica
InventorsTse Wen Chang, Jiun-Bo Chen, Pheidias C. Wu, Alfur F. Hung
Estimating the term…
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.
A CεmX-specific antibody capable of binding to membrane-bound IgE on human B lymphocytes and incapable of binding to RADWPGPP peptide.
A therapeutic method of inducing immune response in patients in vivo by employing an immunogen containing GLAGGSAQSQRAPDRVL or an analogue with similar antigenic property.
A therapeutic method of inducing immune response in patients in vivo by employing an immunogen containing HSGQQQGLPRAAGGSVPHPR or an analogue with similar antigenic property.
A therapeutic method of inducing immune response in patients in vivo by employing an immunogen containing GLAGGSAQSQRAPDRVL or an analogue with similar antigenic property and HSGQQQGLPRAAGGSVPHPR or an analogue with similar antigenic property.
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