Restricted immunoglobulin variable region gene usage by hybridoma rheumatoid factors from patients with systemic lupus erythematosus and rheumatoid arthritis

MM Newkirk, J Rauch, RAK Mageed, R Jefferis… - Molecular …, 1993 - Elsevier
MM Newkirk, J Rauch, RAK Mageed, R Jefferis, DN Posnett, GJ Silverman
Molecular immunology, 1993Elsevier
Rheumatoid factors (RFs) are autoantibodies that are produced by approximately 75% of
patients with rheumatoid arthritis (RA). Their role in pathogenesis is not well understood. In
this study of 81 human hybridoma IgM antibodies derived from unstimulated peripheral
blood B-cells of patients with RA and systemic lupus erythematosus (SLE), we have
demonstrated that idiotypes associated with RFs derived from patients with mixed
cryoglobulinemia were expressed by approximately 60% of RFs and 6% of IgM antibodies …
Rheumatoid factors (RFs) are autoantibodies that are produced by approximately 75% of patients with rheumatoid arthritis (RA). Their role in pathogenesis is not well understood. In this study of 81 human hybridoma IgM antibodies derived from unstimulated peripheral blood B-cells of patients with RA and systemic lupus erythematosus (SLE), we have demonstrated that idiotypes associated with RFs derived from patients with mixed cryoglobulinemia were expressed by approximately 60% of RFs and 6% of IgM antibodies lacking RF activity. The specificity of the RFs for the Fc portion of IgG only (monospecificity) or for Fc and additional self antigens (polyreactivity) was found to correlate with the expression of specific heavy chain associated idiotypes. The V H 3 associated RF idiotypes, D12 and B6, were expressed by 0 16 (0%) of monospecific RFs compared with 6 22 (27%) of polyreactive RFs. The predominant use of V H 3 was verified by analysis of the expressed Ig with VH family specific anti-peptide antibodies. The light chains expressed by both populations of IgM RFs were found to be predominantly VKIII, both by detection of specific epitopes/idiotypes and V family analysis. This non-random gene usage of both the heavy and light chains suggests that there is a selective expression of V regions in the RF producing B-cells in patients with RA and SLE. We suggest that different antigen-driven, clonal selection events may occur which result in either monospecific RFs or polyreactive RFs.
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