Open AccessCharacterization of murine monoclonal antibodies against 60‐kD Ro/SS‐A and La/SS‐B autoantigens
Author(s) -
VELDHOVEN C. H. A.,
PRUIJN G. J. M.,
MEILOF J. F.,
THIJSSEN J. P. H.,
KEMP A. W. C. M.,
VENROOIJ W. J.,
SMEENK R. J. T.
Publication year - 1995
Publication title -
clinical & experimental immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.329
H-Index - 135
eISSN - 1365-2249
pISSN - 0009-9104
DOI - 10.1111/j.1365-2249.1995.tb02275.x
Subject(s) - epitope , microbiology and biotechnology , monoclonal antibody , recombinant dna , epitope mapping , biology , antibody , ribonucleoprotein , antigen , immunofluorescence , immunogenicity , virology , rna , immunology , biochemistry , gene
SUMMARY Small cytoplasmic ribonucleoproteins (scRNPs) are important autoantigens in patients with systemic lupus erythematosus and Sjögren's syndrome. MoAbs against these proteins were made by immunization of BALB/c mice with purified human recombinant 60‐kD Ro/SS‐A or 50‐kD La/SS‐B proteins. Five stable hybridoma cell lines were obtained, of which four secreted anti‐Ro/SS‐A antibodies (clones 1D8, 1D11, 2G10 and 6G8) and one produced anti‐La/SS‐B antibodies (clone 7F6). The MoAbs were further characterized using four different immunoassays: immunofluorescence, immunoblotting, RNA precipitation combined with Northern blotting, and recombinant protein precipitation. All lour MoAbs against Ro/SS‐A recognized the native protein and one of them (2G10) recognized also intact scRNP particles. Interestingly, hY3‐RNA was reproducibly not efficiently precipitated by MoAb 2G10. Epitope mapping using deletion mutants of the 60‐kD Ro/SS‐A antigen showed that MoAb ID8 recognized the C‐terminal part of this protein, while 1D11 and 2G10 recognized distinct epitopes in the region between the RNP motif and the putative zinc finger domain. The epitopes recognized by these MoAbs lire highly conserved among species, and the epitope recognized by MoAb 2G10 may be identical to an autoepitope recognized by sera of patients. This is the first report describing the isolation and characterization of MoAbs of the IgG class against the 60‐kD Ro/SS‐A and La/SS‐B autoantigens obtained by immunization with purified human recombinant proteins. These MoAbs can be of great use in studying the cellular processes in which scRNPs are involved, and may help to determine why these scRNPs become autoantigenic in autoimmune diseases.