Anti-laminin Reactivity and Glomerular Immune Deposition by in Vitro Recombinant Antibodies

References

• Shlomchik M., Marshak-Rothstein A., Wolfowicz C. B., Rothstein T. L., Weigert M. The role of clonal selection and somatic mutation in autoimmunity. Nature 1987; 328: 805–11
   PubMed Web of Science ®Google Scholar
• Marion T., Bothwell A., Briles D., Janeway C. A. IgG anti-DNA autoantibodies within an individual autoimmune mouse are the products of clonal selection. J Immunol. 1989; 142: 4269
   PubMed Web of Science ®Google Scholar
• Limpanasithikul W., Ray S., Diamond B. Cross-reactive antibodies have both protective and pathogenic potential. J Immunol. 1995; 155: 967–973
   Google Scholar
• Reininger L., Berney T., Shibata T., Spertini F., Merino R., Izui S. Cryoglobulinemia induced by a murine lgG3 rheumatoid factor: skin vasculitis and glomerulonephritis arise from distinct pathogenic mechanisms. Proc Natl Acad Sci USA. 1990; 87: 10038–10042
   PubMed Web of Science ®Google Scholar
• Katz M. S., Foster M. H., Madaio M. P. Independently-derived murine glomerular immune deposit forming anti-DNA antibodies are encoded by near identical VH gene sequences. J Clin Invest 1993; 91: 402–408
   PubMedGoogle Scholar
• Ono M., Yamamoto T., Kyogoku M., Nose M. Sequence analysis of the germ-line VH gene corresponding to a nephritogenic antibody in MRL/lpr lupus mice. Clin Exp Immunol. 1995; 100: 284–290
   PubMed Web of Science ®Google Scholar
• Shefner R., Kleiner G., Turken A., Papazian L., Diamond B. A novel class of anti-DNA antibodies identified in BALB/c mice. J Exp Med. 1991; 173: 287–296
   PubMedGoogle Scholar
• Foster M. H., Sabbaga J., Line S. R. P., Thompson K. S., Barrett K. J., Madaio M. P. Molecular analysis of nephrotropic anti-laminin antibodies from an MRL/lpr autoimmune mouse. J Immunol. 1993; 151: 814–824
   PubMedGoogle Scholar
• Stevenson F. K., Longhurst C, Chapman C. J., Ehren-Stein M. R., Spellerberg M. B., Hamblin T. J. Utilization of the VH 4-21 gene segment by anti-DNA antibodies from patients with systemic lupus erythematosus. J Autoimmun. 1993; 6: 809–25
   PubMed Web of Science ®Google Scholar
• Kasturi K. N., Mayer R., Bona C. A., Scott V. E., Sidman C. L. Germline V genes encode viable motheaten mouse autoantibodies against thymocytes and red blood cells. J Immunol 1990; 145: 2304–2311
   PubMed Web of Science ®Google Scholar
• Caulfield M. J., Stanko D. A pathogenic monoclonal antibody, G8: is characteristic of anti-erythrocyte autoantibodies from coombs'-positive NZB mice. J Immunol. 1992; 148: 2068–2073
   Google Scholar
• Lampman G. W., Furie B., Schwartz R. S., Stollar B. D., Furie B. C. Amino acid sequence of a platelet-binding human anti-DNA monoclonal autoantibody. Blood 1989; 74: 262–9
   Google Scholar
• Mariette X., Levy Y., Dubreuil M. L., Intrator L., Danon F., Brouet J. C. Characterization of a human monoclonal autoantibody directed to cardi-olipin/beta 2 glycoprotein 1 produced by chronic lymphocytic leukaemia B cells. Clin Exp Immunol. 1993; 94: 385–90
   PubMed Web of Science ®Google Scholar
• Ray S., Diamond B. Generation of a fusion partner to sample the repertoire of splenic B cells destined for apoptosis. Proc Natl Acad Sci. 1994; 91: 5548–5551
   Google Scholar
• Sambrook J., Fritsch E. F., Maniatis T. Molecular Cloning: A Laboratory Manual. Cold Spring Harbor Laboratory, Cold Spring Harbor, New York 1989
   Google Scholar
• Trepicchio W., Barrett K. J. The lgh-V locus of MRL mice: Restriction fragment length polymorphism in eleven strains of mice as determined with VH and D gene probes. J. Immunol. 1985; 134: 2734–2739
   PubMed Web of Science ®Google Scholar
• Marcu K. B., Banerji J., Penncavage N. A., Lang R., Arnheim N. 5′ flanking region of immunoglobulin heavy chain constant region genes displays length heterogeneity in germlines of inbred mouse strains. Cell. 1980; 22: 187–196
   PubMedGoogle Scholar
• Nemazee D. A., Burki K. Clonal deletion of B lymphocytes in a transgenic mouse bearing anti-MHC class I antibody genes. Nature 1989; 337: 562–566
   PubMed Web of Science ®Google Scholar
• Russell D. M., Dembic Z., Morahan G., Miller J. F. A. P., Burki K., Nemazee D. Peripheral deletion of self-reactive B cells. Nature 1991; 354: 308–311
   PubMed Web of Science ®Google Scholar
• McBurney M. W., Sutherland L. C, Adra C. N., Leclair B., Rudnicki M. A., Jardine K. The mouse Pgk-1 gene promoter contains an upstream activator sequence. Nucleic Acids Res. 1991; 19: 5755–5761
   PubMedGoogle Scholar
• Carson D., Weigert M. Immunochemical analysis of the cross-reacting idiotypes of mouse myeloma proteins with anti-dextran activity and normal anti-dextran antibody. Proc Natl Acad Sci USA. 1973; 70: 235–239
   Google Scholar
• Gillies S. D., Morrison S. L., Oi V. T., Tonegawa S. A tissue-specific transcription enhancer element is located in the major intron of a rearranged immunoglobulin heavy chain gene. Cell. 1983; 33: 717–728
   PubMed Web of Science ®Google Scholar
• Oi V., Morrison S. L., Herzenberg L. A., Berg P. Immunoglobulin gene expression in transformed lymphoid cells. Proc Natl Acad Sci USA. 1983; 80: 825–829
   PubMed Web of Science ®Google Scholar
• Vlahakos D. V., Foster M. H., Adams S., Katz M., Ucci A. A., Barrett K. J. Anti-DNA antibodies form immune deposits at distinct glomerular and vascular sites. Kidney Int. 1992; 41: 1690–1700
   PubMed Web of Science ®Google Scholar
• Foster M. H., MacDonald M., Barrett K. J., Madaio M. P. VH gene analysis of spontaneously activated B cells in adult MRL-lpr/lpr mice. The J558 bias is not limited to classic lupus autoantibodies. J Immunol. 1991; 147: 1504–1511
   Google Scholar
• Hoogenraad N. J., Wraight C. J. The effect of pristane on ascites tumor formation and monoclonal antibody production. Methods Enzymol. 1986; 121: 375
   Google Scholar
• Foster M. H., Cizman B., Madaio M. P. Nephritogenic autoantibodies in systemic lupus erythematosus: Immunochemical properties, mechanisms of immune deposition and genetic origins. Lab Invest. 1993; 69: 494–507
   PubMedGoogle Scholar
• Marion T. N., Tillman D. M., Krishnan M. K., Desai D. D., Jou N., Ruff M. B. Immunoglobulin variable-region structures in immunity and autoimmunity to DNA. Tohoku J Exp Med. 1994; 173: 43–63
   Google Scholar
• Radic M. Z., Weigert M. G. Genetic and structural evidence for antigen selection of anti-DNA antibodies. Annu Rev Immunol. 1994; 12: 487
   PubMed Web of Science ®Google Scholar
• Hirabayashi Y., Munakata Y., Takai O., Shibata S., Sasaki T., Sano H. Human B-cell clones expressing lupus nephritis-associated anti-DNA idiotypes are preferentially expanded without somatic mutation. Scand J Immunol. 1993; 37: 533–540
   PubMed Web of Science ®Google Scholar
• Katz J. B., Limpanasithikul W., Diamond B. Mutational analysis of an autoantibody: differential binding and pathogenicity. J Exp Med. 1994; 180: 925–932
   PubMed Web of Science ®Google Scholar
• Bruijn J., van Leer E., Baelde H., Corver W., Hogen-Doorn P., Fleuren G. Characterization and in vivo transfer of nephritogenic autoantibodies directed against dipeptidyl peptidase IV and laminin in experimental lupus nephritis. Lab Invest. 1990; 63: 350–359
   PubMedGoogle Scholar
• Florquin S., Abramowicz D., de Heer E., Bruijn J. A., Doutrelepont J. M., Goldman M. Renal immunopathology in murine host-versus-graft disease. Kidney Int. 1991; 40: 852–61
   Google Scholar
• Ibrahim S. M, Weigert M, Basu C, Erikson J., Radic M. Z. Light chain contribution to specificity in anti-DNA antibodies. J Immunol. 1995; 155: 3223–3233
   Google Scholar
• Abrahamson D. R., Irwin M. H., John P. L. S., Perry E. W., Accavitti M. A., Heck L. W. Selective immunoreactivities of kidney basement membranes to monoclonal antibodies against laminin: Localization of the end of the long arm and the short arms to discrete microdomains. J Cell Biol. 1989; 109: 3477–3491
   PubMed Web of Science ®Google Scholar
• Kleinman H. K., Weeks B. S., Schnaper H. W., Kibbey M. C, Yamamura K., Grant D. S. The laminins: A family of basement membrane glycoproteins important in cell differentiation and tumor metastases. Vitamins and Hormones 1993; 47: 161–186
   PubMed Web of Science ®Google Scholar
• Abrass C. K., Spicer D., Raugi G. J. Insulin induces a change in extracellular matrix glycoproteins synthesized by rat mesangial cells in culture. Kidney Internal. 1994; 46: 613–620
   Google Scholar
• Ekblom M., Klein G., Mugrauer G., Fecker L., Deutz-Mann R., Timpl R. Transient and locally restricted expression of laminin A chain mRNA by developing epithelial cells during kidney organogenesis. Cell. 1990; 60: 337–346
   PubMed Web of Science ®Google Scholar
• Tokida Y., Aratani Y., Morita A., Kitagawa Y. Production of two variant laminin forms by endothelial cells and shift of their relative levels by angiostatic steroids. J Biol Chem. 1990; 265: 18123–18129
   PubMed Web of Science ®Google Scholar
• Satoh M., Reeves W. H. Induction of lupus-associated autoantibodies in BALB/c mice by intraperitoneal injection of pristane. J Exp Med. 1994; 180: 2341–2346
   PubMed Web of Science ®Google Scholar