Medical College of Wisconsin
CTSICores SearchResearch InformaticsREDCap

Human monoclonal striational autoantibodies isolated from thymic B lymphocytes of patients with myasthenia gravis use VH and VL gene segments associated with the autoimmune repertoire. Eur J Immunol 1992 Sep;22(9):2231-6

Date

09/01/1992

Pubmed ID

1516616

DOI

10.1002/eji.1830220908

Scopus ID

2-s2.0-0026775966 (requires institutional sign-in at Scopus site)   23 Citations

Abstract

The production of autoantibodies reactive with components of skeletal muscle is characteristic of myasthenia gravis (MG) and is strongly associated with the presence of thymic epithelial tumors in patients with MG. The nucleotide sequences of the heavy and light chain variable regions (VH and VL) of three human monoclonal striated muscle antibodies (StrAb) isolated from thymic B lymphocyte lines from two patients with MG and thymoma were analyzed. The VH and VL gene segments used by these anti-striated muscle antibodies appear to be derived from the same repertoire of gene segments as have been found in other autoantibodies isolated from patients with a number of different autoimmune diseases. While the IgM StrAb SA-1A is a direct copy of germ-line VH and VL gene segments, analysis of the IgG StrAb SA-4A and SA-4B, which may be more representative of antibodies found in the serum of MG patients, suggests that the processes of antigenic selection and somatic mutation may contribute to the generation of autoantibodies in MG.

Author List

Victor KD, Pascual V, Williams CL, Lennon VA, Capra JD

Author

Carol L. Williams PhD Professor in the Pharmacology and Toxicology department at Medical College of Wisconsin




MESH terms used to index this publication - Major topics in bold

Actins
Amino Acid Sequence
Antibodies, Monoclonal
Autoantibodies
B-Lymphocytes
Base Sequence
Connectin
Genes, Immunoglobulin
Humans
Immunoglobulin Heavy Chains
Immunoglobulin Light Chains
Immunoglobulin Variable Region
Molecular Sequence Data
Muscle Proteins
Muscles
Myasthenia Gravis
Protein Kinases