Drug intelligence / Profile preview

APLDQ-cβ3-E2-Fc

Development stage
Preclinical
Lead developer
BloodCenter of Wisconsin
Modality
Fc-Fusion Proteins → Carrier/Scaffold Proteins → Recombinant Proteins and Enzymes
Administration
Intravenous, Intraperitoneal
01

Overview

APLDQ-cβ3-E2-Fc is a chimeric HPA-1a-containing Fc fusion protein designed as a targeted immunotherapy for fetal and neonatal alloimmune thrombocytopenia (FNAIT). It is composed of an α-subunit-independent murine single-chain chimeric β3 integrin fragment (cβ3-E2) that incorporates five humanized amino acids (A30, P32, L33, D39, Q47) to express the human HPA-1a epitope, fused to the Fc region of mouse IgG2a. The therapeutic mechanism involves selectively neutralizing and clearing circulating maternal anti-HPA-1a alloantibodies and depleting HPA-1a-specific antibody-producing B cells. By targeting the root cause of pathogenic alloantibody generation, APLDQ-cβ3-E2-Fc aims to provide an antigen-specific alternative to non-specific immunosuppressive treatments like IVIG or FcRn-blocking antibodies.

Other names
APLDQ-cbeta3-E2-FcAPLDQ-cbeta-3-E2-FcAPLDQ-cbeta 3-E2-FcHPA-1a-containing Fc fusion proteinHPA1a-containing Fc fusion proteinHPA 1a-containing Fc fusion protein
02

Targets

Human platelet antigen 1a-specific B-cell receptorFcγR (Low affinity immunoglobulin gamma Fc region receptor II-c)Anti-HPA-1a (Anti-human platelet antigen-1a alloantibody)FCGRT (Neonatal crystallizable fragment receptor)

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