A monoclonal antibody against NeuGc-containing gangliosides contains a regulatory idiotope involved in the interaction with B and T cells

• Published in: Molecular immunology 2002-09, Vol.39 (1), p.103-112
• Main Authors: Perez, Alexis, Mier, Elin S, Vispo, Nelson Santiago, Vazquez, Ana Maria, Perez Rodrı́guez, Rolando
• Format: Article
• Language: English
• Subjects: Amino Acid Sequence; Animals; Antibodies, Monoclonal - immunology; B-Lymphocytes - immunology; Complementarity Determining Regions; Female; Gangliosides - immunology; H-CDR3; Idiotype; Immunization; Immunoglobulin Idiotypes - immunology; Mice; Mice, Inbred BALB C; Molecular Sequence Data; Monoclonal antibody; N-Glycolyl neuraminic acid; Neuraminic Acids - immunology; T-Lymphocytes - immunology
• ISSN: 0161-5890; 1872-9142
• DOI: 10.1016/S0161-5890(02)00041-X

P3 (IgM-κ) is a monoclonal antibody (mAb) reacting with N-glycolyl neuraminic acid (NeuGc)-containing gangliosides and sulfated glycolipids. To explore the nature of the idiotope defined by 1E10, we used a phage-displayed random peptide library. After three rounds of selection, seven different phagotopes were isolated. Noteworthy, all the sequences were found to bear the basic amino acid-rich motifs KPPR (3) or RRPR/K (4). This recursive selection of basic sequences by 1E10 mAb confirmed previous suggestions of the involvement of charged residues in the interaction between γ-type Ab2 and P3 mAb. The binding of 1E10 to phage peptides representing each group was completely inhibited by P3 mAb. In addition, other Ab2 to P3 were able to recognize these peptides. Thus, phage peptides seem to be mimotopes of the idiotope recognized by anti-idiotypic antibodies in P3. Phage motifs were represented in the lineal sequence of P3’s heavy chain H-CDR3 and a 14-mer peptide representing this region was able to specifically inhibit 1E10 binding to P3. Previous studies showed that P3’s idiotype was autoimmunogenic and shared by antibodies with different specificities. Now, we demonstrated that P3 mAb is able to activate a network cascade involving autologous anti-idiotypic and anti-anti-idiotypic T cells. Thus, P3’s idiotype fulfill the three criteria previously established to define a “regulatory idiotype”. Particularly, data presented here revealed the immunodominance of the H-CDR3 of this mAb as a T cell epitope. Thus, H-CDR3 is simultaneously involved in the interaction of P3 mAb with anti-idiotypic B and T cells, behaving as a potential regulatory idiotope.