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CD22 is a transmembrane glycoprotein receptor and a member of the immunoglobulin superfamily, predominantly expressed on the surface of mature B lymphocytes[2][4][5][7]. It binds sialic acid-containing glycans via its N-terminal Ig domain and acts as an inhibitory co-receptor that regulates B-cell receptor (BCR) signaling by recruiting cytoplasmic phosphatases (e.g., SHP-1) upon tyrosine phosphorylation in response to antigen stimulation[1][3][4]. CD22 thereby dampens BCR-mediated signaling, sets activation thresholds in B cells, and plays a critical role in immune tolerance and prevention of autoimmunity[1][2][4]. Its targeted modulation is clinically relevant in autoimmunity and B-cell malignancies, and it is the molecular target of several approved or investigational therapeutic antibodies and antibody-drug conjugates[4][5].
Monoclonal antibodies binding to CD22 block BCR signaling or mediate antibody-dependent cell cytotoxicity (ADCC) Antibody-drug conjugates deliver cytotoxins to CD22-expressing B cells Target engagement leads to internalization and inhibition of B-cell survival[4][5]
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