Nucleotidic sequence analysis of the variable domains of four human monoclonal IgM with an antibody activity to myelin-associated glycoprotein

• Published in: European journal of immunology Vol. 23; no. 4; p. 846
• Main Authors: Mariette, X, Tsapis, A, Brouet, J C
• Format: Journal Article
• Language: English
• Published: Germany 01-04-1993
• Subjects: Amino Acid Sequence; Antibodies, Monoclonal - immunology; Base Sequence; Clone Cells; Genes, Immunoglobulin; Glycoproteins - immunology; Humans; Immunoglobulin kappa-Chains - genetics; Immunoglobulin M - genetics; Immunoglobulin mu-Chains - genetics; Immunoglobulin Variable Region - genetics; Molecular Sequence Data; Myelin Proteins - immunology; Myelin-Associated Glycoprotein; Nerve Tissue Proteins - immunology; Oligodeoxyribonucleotides - chemistry; Sequence Alignment
• ISSN: 0014-2980
• DOI: 10.1002/eji.1830230412

We determined the nucleotide sequence of the VL and VH regions of four human monoclonal IgM directed to myelin-associated glycoprotein (MAG) and a nerve glycolipid, the sulfated glucuronic paragloboside (SGPG). Clonal lymphoblastoid cell lines (three cases) and an heterohybridoma (one case) secreting anti-MAG IgM were derived from patients' blood B cells. V kappa genes derived from the single germinal V kappa IV (two cases), the V kappa Id and the V kappa IIIa Humkv328h5 genes. VH genes derived from the VHIII 9.1 germinal gene (or a closely related gene) in two cases, whereas two others possibly represent new members of the VHIII or VHI variability subgroups. There was no obvious restriction in the use of J kappa, JH and DH segments. Somatic mutations were predominantly found in the CDR3 of the V kappa IV genes with an overall ratio of replacement over silent mutations of 7/0. The sequence of two VHIII genes exhibited five replacement mutations in CDR in comparison to that of the germ-line 9.1 gene. Although some V genes are likely to be overrepresented among anti-MAG IgM, the diversity of the immune repertoire for MAG and SGPG explains the lack of easily detectable public idiotopes among these IgM. This last finding, as well as a high ratio of replacement versus silent nucleotide mutations in the CDR of VL and probably VH genes, suggest that the pathogenesis of these monoclonal antibodies (and of the associated lymphoplasmocytic disorder) differs from that of other previously characterized monoclonal autoantibodies such as rheumatoid factors and cold agglutinins.