Immunological analysis of the amino terminal and the C8 isomer of human myelin basic protein

Abstract

The citrullination and N-terminus acylation of myelin basis protein (MBP) increases the heterogeneity among the MBP isoforms. The present study was undertaken to further characterize the immune response to the citrullinated from (C8) of MBP as well as to the variably acylated N-terminus of MBP. Six well-characterized murine monoclonal antibodies (mAbs) to human MBP-C8 or MBP peptides (four mAbs to MBP acetyl 1–9, one mAb to MBP 10–19 and one mAb to MBP 80–89), one murine T cell line (PL11) to human MBP peptide acetyl 1–9 and one Lewis rat T cell line (RT-1) to guinea pig (GP) MBP peptide 68–88 were used to assess reactivity with MBP-C1, MBP-C8, and MBP peptides including a series of MBP peptide 1–21 containing 0, 2, 4, 6, 8 or 10 carbon fatty acids. Enzyme-linked immunosorbent assay (ELISA) results revealed that all of the mAbs reacted with human MBP-C1 and MBP-C8 except anti-MBP 10–19 and anti-MBP-C8. The former reacted only with MBP-C1 and the latter only with MBP-C8. The presence and length of acylation of MBP peptide 1–21 modified reactivity. Three mAbs to MBP acetyl 1–9 reacted only with acetyl 1–21, and one mAb anti-MBP acetyl 1–9 reacted with all of MBP 1–21 preparations whether acylated or not. mAb anti-MBP-C8 generally reacted better with acylated MBP 1–21 having longer fatty acids. The PL11 T cell line strongly proliferated to human MBP-C1, MBP-C8 and MBP acetyl 1–9, responded, but less well, to MBP 1–21 with longer fatty acids and failed to respond to nonacylated MBP peptide 1–21. The RT-1 cell line responded strongly to GP MBP peptide 68–88, marginally to MBP-C8 and failed to respond to MBP-C1 or any of the other MBP peptides. Specific immune responses to different MBP charge isomers and different N-terminal acylating groups of MBP may play a role in immune-mediated demyelination.