Analysis of immunoglobulins secreted by hybridomas derived from rheumatoid synovia
- PMID: 2115418
- PMCID: PMC1535208
- DOI: 10.1111/j.1365-2249.1990.tb03294.x
Analysis of immunoglobulins secreted by hybridomas derived from rheumatoid synovia
Abstract
Twenty-six IgG-secreting and eight IgM-secreting hybridomas were derived from the synovia of two patients with rheumatoid arthritis (RA). Hybridomas were obtained by fusing a heteromyeloma cell line, SPAZ-4 with synovial mononuclear cells that were not deliberately stimulated in vitro. Over 96% of the IgG-secreting hybridomas produced antibodies which belonged to the IgG1 subclass and showed lambda light chain predominance; the latter was not seen in IgM antibodies, where kappa light chains dominated by 3:1. All IgG antibodies were cationic. Synovial B cells were not exposed to extrinsic stimuli prior to fusion, therefore these results reflect the state of B cell activation and differentiation in vivo. Our results indicate that IgG-secreting B cells in the RA joint are under a selective influence which is, as yet, unidentified. One out of eight IgM-secreting and two out of 26 IgG-secreting hybridomas produced rheumatoid factors (RF). The IgM-RF specificity for IgG heavy chain subclasses was determined and showed that the monoclonal bound to IgG1, IgG2 and IgG4 but not IgG3 with exception of IgG3 Goe of the G3m (st) allotype, a profile typical of specificity for the Ga epitope. This monoclonal also distinguished a determinant in the Fc region of human IgG which was not present in rabbit IgG. The overall frequency of RF-secreting hybridomas we observed indicates that B cells committed to RF production in the synovium of a seropositive and a seronegative RA patient is below 10%.
Similar articles
-
Immunoglobulin heavy chain variable region gene utilization by B cell hybridomas derived from rheumatoid synovial tissue.Clin Exp Immunol. 1992 Aug;89(2):230-8. doi: 10.1111/j.1365-2249.1992.tb06937.x. Clin Exp Immunol. 1992. PMID: 1379132 Free PMC article.
-
Characterization of monoclonal IgG antibodies produced by hybridomas derived from rheumatoid synovial cells.Hum Antibodies Hybridomas. 1992 Apr;3(2):60-4. Hum Antibodies Hybridomas. 1992. PMID: 1633266
-
Monoclonal IgM, IgG, and IgA human rheumatoid factors produced by synovial tissue-derived, EBV-transformed B cell lines.Clin Immunol Immunopathol. 1993 Jan;66(1):18-25. doi: 10.1006/clin.1993.1003. Clin Immunol Immunopathol. 1993. PMID: 8382569
-
IgG3 reactive rheumatoid factor in rheumatoid arthritis: etiologic and pathogenic considerations.Autoimmunity. 1994;19(3):199-210. doi: 10.3109/08916939408995695. Autoimmunity. 1994. PMID: 7541651 Review.
-
T and B cell-dependent pathways in rheumatoid arthritis.Curr Opin Rheumatol. 1995 May;7(3):214-21. doi: 10.1097/00002281-199505000-00010. Curr Opin Rheumatol. 1995. PMID: 7612413 Review.
Cited by
-
Immunoglobulin heavy chain variable region gene utilization by B cell hybridomas derived from rheumatoid synovial tissue.Clin Exp Immunol. 1992 Aug;89(2):230-8. doi: 10.1111/j.1365-2249.1992.tb06937.x. Clin Exp Immunol. 1992. PMID: 1379132 Free PMC article.
-
Sequence analysis of immunoglobulin heavy-chain variable region genes from the synovium of a rheumatoid arthritis patient shows little evidence of mutation but diverse CDR3.Immunology. 1995 Mar;84(3):367-74. Immunology. 1995. PMID: 7751018 Free PMC article.
-
Remarkably similar antigen receptors among a subset of patients with chronic lymphocytic leukemia.J Clin Invest. 2004 Apr;113(7):1008-16. doi: 10.1172/JCI19399. J Clin Invest. 2004. PMID: 15057307 Free PMC article.
-
A flow cytometry-based strategy to identify and express IgM from VH1-69+ clonal peripheral B cells.J Immunol Methods. 2011 Jan 5;363(2):210-20. doi: 10.1016/j.jim.2010.09.022. Epub 2010 Sep 24. J Immunol Methods. 2011. PMID: 20875420 Free PMC article.
-
A human monoclonal IgA rheumatoid factor using the VkIV light chain gene.Rheumatol Int. 1992;12(1):23-31. doi: 10.1007/BF00246873. Rheumatol Int. 1992. PMID: 1598498
References
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Medical