Antibodies to Synthetic Platelet-Activating Factor (1-O-Alkyl-2- O-Acetyl-sn-Glycero-3-Phosphocholine) Analogues with Substituents at the sn-2 Position

We obtained rabbit antibodies by injecting immunogenic conjugates which were prepared by combining covalenily l-O-(15′ carboxypeitadecyl)-2-0-acetyl-snaycero-3-phospbflcboline(ace-tyl-CPGPC), l-O-(15′-carboxypentadecyl)-2-O-N, N-dimethylcarbamoyl-sn-glycero-3-phosphocholine (dimethylcarbamoyl-CPGPC), or 1-o-(15′-carboxypentadecyl)-2-o-N-butyl-carbamoyl-sn-glycero-3-phosphocholine (butylcarbamoyl-CPGPC) with protein (BSA or KLH), respectively, and examined the specificity of the resulting antibodies by comparison with inhibition of the binding of iodolabeled CPGPC derivatives to the antibodies by corresponding or related phospholipids. Acetyl-CPGPC and dimethylcarbamoyl-CPGPC possessed haptenic activity causing production of antibodies reactive with PAF. Changes of the substituents at sn-2 in the antigens affected the specificity of the resulting antibodies. The affinity of the substituents to the antibodies decreased in the following order: acetyl ≫ dimethylcarbamoyl and butylcarbamoyl for antibodies to acetyl-CPGPC-KLH; dimethylcarbamoyl> acetyl ≫butylcarbamoyl for antibodies to dimethylcarbamoyl-CPGPC-BSA; and butylcarbamoyl> dimethylcarbamoyl > acetyl for antibodies to butylcarbamoyl-CPGPC-BSA. Naturally occurring phospholipids, including lysoPAF, phosphatidylcholine, lyso-phosphatidylcholine, and sphingomyelin, revealed no cross-reactivities with these antibodies. Anti-dimethylcarbamoyl-CPGPC-BSA IgG and anti-acetyl-CPGPC-KLH IgG inhibited a PAF-induced aggregation of washed rabbit platelets in a dose-dependent manner. In contrast, anti-butylcarbamoyl-CPGPC-BSA IgG did not affect a PAF-induced platelet aggregation, nor did preimmune IgG.