Molecular analysis of the heavy chain variable region genes of human hybridoma clones specific for coagulation factor VIII

• Published in: Thrombosis and haemostasis Vol. 94; no. 6; p. 1131
• Main Authors: Gharagozlou, Soheila, Kardar, Gholam Ali, Rabbani, Hodjattallah, Shokri, Fazel
• Format: Journal Article
• Language: English
• Published: Germany 01.12.2005
• Subjects: Adult; Amino Acid Sequence; Antibodies, Monoclonal - chemistry; Antibodies, Monoclonal - genetics; Base Sequence; Cells, Cultured; Factor VIII - antagonists & inhibitors; Factor VIII - immunology; Factor VIII - therapeutic use; Hemophilia A - blood; Hemophilia A - drug therapy; Hemophilia A - immunology; Humans; Hybridomas; Immunoglobulin Heavy Chains - chemistry; Immunoglobulin Heavy Chains - genetics; Immunoglobulin Variable Region - chemistry; Immunoglobulin Variable Region - genetics; Middle Aged; Molecular Sequence Data; Protein Conformation; Sequence Alignment
• ISSN: 0340-6245
• DOI: 10.1160/TH05-06-0445

HemophiliaA is a X-linked hematologic disorder characterized by undetectable or low amounts of functional coagulation factor VIII (FVIII). Replacement therapy induces FVIII neutralizing antibody (Ab) (inhibitor) in a proportion of patients which makes further treatment of these patients ineffective and costly. To envisage mechanisms underlying inhibitor development, seven hybridoma clones specific for FVIII were generated from two hemophilia A patients with high titer of inhibitor. Specificity and isotype of the monoclonal antibodies (mAbs) were determined by ELISA. Immunoglobulin (Ig) variable region heavy (VH) chain gene family usage was identified by RT-PCR using VH1-6 specific primers. Nucleotide sequences of the VH gene of FVIII specific clones were determined and aligned to the most homologous germ line genes in the GenBank. Analysis of the expressed VH genes by RT-PCR revealed that the hybridomas utilized either the VH1 (71%) or the VH3 (29%) gene family. Three VH domains were encoded by V1-69 (DP-10),V1-2 (DP-8), and V1-8 (DP-15) genes and two by V1-18 (DP-14) gene, all from the VH1 gene family. Of theVH3-gene family expressing clones, one belonged to V3-66 (DP-86) and the other one to V3-21 (DP-77) germline genes. The CDR3 length was found to be highly different amongst these clones ranging from 11 to 22 amino acid residues. These data suggest that FVIII-specific Abs preferentially use VH gene segments derived from VH1 gene family. Diversity of the expressed VH genes and their CDR3 length implies that different epitopes are recognized by these mAbs.