CHARACTERIZATION OF HUMAN BLOOD-GROUP SCFV ANTIBODIES DERIVED FROM A V-GENE PHAGE-DISPLAY LIBRARY

We previously reported the initial characterization of five human single-chain Fv (scFv) antibody fragments specific for the blood group antigens B, D(Rh), E(Rh), Kp(b) and HI. The scFvs were isolated from a phage-antibody library constructed from the variable region genes of two non-immunized donors. In this paper we report the specificity, affinity and kinetics of antigen binding of these scFv fragments. All five scFVs agglutinated the appropriate red cell phenotype following the addition of a monoclonal antibody which recognizes a peptide tag incorporated into the scFv. The anti-B and anti-HI scFv molecules, which recognize high density carbohydrate antigens, spontaneously polymerized and agglutinated red cells directly. None of the antibody fragments showed cross-reactivity with other red cell antigens, with the exception of the anti-E which reacted weakly with E-negative cells. Specific scFv binding was confirmed by ELISA, flow cytometry and radioactive labelling. The anti-D scFv recognized 17600 sites on cDE/cDE red cells with an association constant (K,), of 5.2 x 10(7)M(-1) and a rate constant for dissociation (k(off)) Of 1.9 x 10(-2) s(-1). The anti-E scFv recognized 29800 and 39800 sites on cDE/cDE red cells in two experiments with K(a)s of 8.4 x 10(6) and 5.1 x 10(7) M(-1). The k(off) for this antibody was 2.7 x 10(-2) s(-1). The results demonstrate that scFv antibody fragments specific for cell surface antigens and possessing affinities typical of the primary immune response can be obtained from a phage-display library.