AFP1 antibodies are recombinant or monoclonal immunoglobulins engineered to bind AFP with high specificity. Key features include:
Specificity: AFP1 antibodies show no cross-reactivity with albumin or other serum proteins, validated using knockout cell lines (e.g., HepG2 AFP-KO) .
Epitope Binding: Some antibodies target cyclic peptide domains (e.g., AFPep) to block estrogen receptor signaling in breast cancer .
AFP1 antibodies are critical in diagnosing and monitoring cancers:
Localizes AFP in hepatocellular carcinoma tissues (Fig. S1A ) and embryoid bodies during stem cell differentiation .
Detects AFP in ascitic fluid and plasma at sensitivities as low as 10 µg/mL .
Identifies intracellular AFP in permeabilized HepG2 cells, with signal intensity correlating to tumor progression .
AFP1 antibodies are explored for targeted drug delivery and immunotherapy:
AFP’s hydrophobic pocket binds chemotherapeutics (e.g., doxorubicin), releasing them in acidic tumor microenvironments .
Conjugation with toxins (e.g., diphtheria toxin) enhances cytotoxicity in AFP-positive tumors .
AFP-derived helper T-lymphocyte (HTL) epitopes (e.g., AFP 1: MKWVESIFLIFLLNFTESRT) stimulate immune responses in HCC patients, improving survival rates in stages II–IV .
AFP1 antibodies are pivotal in:
Early Detection: Elevated AFP-L3 levels correlate with HCC recurrence post-resection .
Therapeutic Monitoring: T-cell responses to AFP epitopes predict immunotherapy efficacy in clinical trials .
Future research aims to refine AFP1 antibody conjugates for reduced off-target effects and improved tumor penetration .