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Light Chain Variable (V L ) Sequences of Rheumatoid Factors (RF) in Patients with Primary Sjögren's Syndrome (pSS): Moderate Contribution of Somatic Hypermutation
Author(s) -
Elagib,
Boslash;rretzen,
Wesley K. Thompson,
Natvig
Publication year - 1999
Publication title -
scandinavian journal of immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.934
H-Index - 88
eISSN - 1365-3083
pISSN - 0300-9475
DOI - 10.1046/j.1365-3083.1999.00624.x
Subject(s) - immunoglobulin light chain , somatic hypermutation , rheumatoid factor , gene , germline , kappa , microbiology and biotechnology , antibody , somatic cell , germline mutation , mutation , biology , genetics , gene mutation , b cell , virology , linguistics , philosophy
We have characterized and sequenced the variable (V) region genes of the light (L) chains of 10 immunoglobulin (IgM) rheumatoid factor (RF) monoclonal antibodies (MoAb) derived by the hybridoma/Epstein‐Barr virus (EBV) technique from the peripheral blood of patients with primary Sjögren's syndrome (pSS). Six out of 10 RFs used lambda (λ) L chains, while four RFs used kappa (κ) L chains. Five out of the six λ RFs were encoded by V λ 3 gene segments, the sixth one was encoded by a V λ 1 gene segment. This preferential utilization of the V λ 3 family genes suggests selective expansion of the B cell in pSS. Three of the κ RFs used V κ 3 gene segments, while the fourth used a V κ 2 gene segment. Half of the RFs were found as unmutated copies of their closest germline (GL) gene. Interestingly these RFs were previously shown to use heavy (H) chains in GL gene configuration. Three RFs have very few mutations (2–3) and only two RFs have substantial numbers of mutations (6 and 11). This also correlated with the number of mutations in the respective H chains. In contrast to RFs in normal and RA these results further suggest the somatic mutation to be of moderate importance in the generation of RF from the peripheral blood of pSS patients.