Hydroxyl Radical Modification of Polyguanylic Acid: Role of Modified Guanine in Circulating SLE Anti‐DNA Autoantibodies

References

• Ahmad J., Ashok B. T., Ali R. Reactive oxygen species modified thymine and poly (dT) represent unique epitope for human anti‐DNA autoantibodies. Immunol. Lett. 1997, 58: 69–74
   PubMedGoogle Scholar
• Ali R., DerSimonian H., Stollar B. D. Binding of monoclonal anti‐native DNA autoantibodies to DNA of varying size and conformation. Mol. Immunol. 1985, 22: 1415–1422
   PubMedGoogle Scholar
• Aotsuka S., Okawa M., Ikebe K., Yokohari R. Measurement of anti‐double stranded DNA antibodies in major immunoglobulin classes. J. Immunol. Methods 1979, 28: 149–162
   PubMedGoogle Scholar
• Ara J., Ali R. Reactive oxygen species modified DNA fragments of varying size are the preferred antigen for human anti‐DNA autoantibodies. Immunol. Lett. 1992, 34: 195–200
   PubMedGoogle Scholar
• Ara J., Ali R. Polynucleotide specificity of anti‐ROS DNA antibodies. Clin. Exp. Immunol. 1993, 94: 134–139
   PubMedGoogle Scholar
• Ara J., Ali R. Antigenic specificity of anti‐ROS DNA antibodies: involvement of lysyl residues in antigen binding. Biochem. Int. 1995, 35: 213–222
   Google Scholar
• Arnett F. C., Edworthy S. M., Bloch D. A., McShane D. J., Fries J. F., Cooper N. S., Healy L. A., Kaplan S. R., Liang M. H., Luthra H. S., Medsger T. A., Jr., Mitchell D. M., Neustadt D. H., Pinals R. S., Schaller J. G., Sharp J. T., Wilder R. L., Hunder G. G. The American Rheumatism Association 1987 revised criteria for the classification of rheumatoid arthritis. Arth. Rheum. 1988, 31: 315–324
   PubMedGoogle Scholar
• Ashok B. T., Ali R. Antigen binding characteristics of experimentally‐induced antibodies against hydroxyl radical modified native DNA. Autoimmunity 1999, 29: 11–19
   PubMedGoogle Scholar
• Bashir S., Harris G., Denman M. A., Blake D. R., Winyard P. G. Oxidative DNA damage and cellular sensitivity to oxidative stress in human autoimmune diseases. Ann. Rheum. Dis. 1993, 52: 659–666
   PubMedGoogle Scholar
• Blount S., Griffiths H. R., Lunec J. Reactive oxygen species modify human DNA. Eliciting a more discriminating antigen for the diagnosis of systemic lupus erythematosus. Clin. Exp. Immunol. 1990, 81: 384–389
   PubMedGoogle Scholar
• Breen A. P., Murphy J. A. Reactions of oxyl radicals with DNA. Free Rad. Biol. Med. 1995, 18: 1033–1077
   PubMedGoogle Scholar
• Cheng K. C., Cahill D. S., Kasai H., Nishimura S., Loeb L. A. 8‐Hydroxy‐guanine, an abundant form of oxidative DNA damage, causes G‐T and A‐C substitution. J. Biol. Chem. 1992, 267: 166–172
   PubMedGoogle Scholar
• Cooke M. S., Mistry N., Wood C., Herbert K. E., Lunec J. Immunogenicity of DNA damaged by reactive oxygen species. Implications for anti‐DNA antibodies in lupus. Free Rad. Biol. Med. 1997, 22: 151–159
   PubMedGoogle Scholar
• Dizdaroglu M. Chemical determination of free radical induced damage to DNA. Free Rad. Biol. Med. 1991, 10: 225–242
   PubMedGoogle Scholar
• Dizdaroglu M. Chemical determination of oxidative DNA damage by gas chromatography mass spectrometry. Method Enzymol. 1994, 234: 3–16
   PubMedGoogle Scholar
• Dziarski R. Autoimmunity: polyclonal activation or antigen induction. Immunol. Today 1988, 9: 340–342
   PubMedGoogle Scholar
• Goding J. W. Use of Staphylococcal Protein‐A as immunological reagent. J. Immunol. Methods 1978, 20: 241–253
   PubMedGoogle Scholar
• Halliwell B., Aruoma O. I. DNA damage by oxygen‐derived species. Its mechanism and measurement in mammalian systems. FEBS Lett. 1991, 281: 9–19
   PubMedGoogle Scholar
• Hasan R., Ali R. Antibody recognition of common epitopes on Z‐DNA and native DNA brominated under high salt. Biochem. Int. 1990, 20: 1077–1088
   PubMedGoogle Scholar
• Hasan R., Ali A., Ali R. Antibodies against DNA‐psoralen crosslinks recognize unique conformation. Biochim. Biophys. Acta 1991, 1073: 507–513
   Google Scholar
• Kasai H. Analysis of a form of oxidative DNA damage, 8‐hydroxy‐2′‐deoxyguanosine, as a marker of cellular oxidative stress during carcinogenesis. Mut. Res. 1997, 387: 147–163
   PubMedGoogle Scholar
• Klinman D. M., Eisenberg R. A., Steinberg A. D. Development of autoimmune B cell repertoire in MRL‐lpr/Gsr mice. J. Immunol. 1990, 144: 506–511
   PubMedGoogle Scholar
• Loft S., Poulsen H. E. Cancer risk and oxidative DNA damage in man. J. Mol. Med. 1996, 74: 297–312
   PubMedGoogle Scholar
• Lunec J., Herbert K., Blount S., Griffiths H. R., Emery P. 8‐Hydroxy deoxyguanosine: a marker of oxidative DNA damage in systemic lupus erythematosus. FEBS Lett. 1994, 348: 131–138
   PubMedGoogle Scholar
• Madaio M. P., Hodder S., Schwartz R. S., Stollar B. D. Responsiveness of autoimmune and normal mice to nucleic acid antigens. J. Immunol. 1984, 132: 872–876
   PubMedGoogle Scholar
• Musarrat J., Wani A. A. Quantitative immunoanalysis of promutagenic 8‐hydroxy‐2‐deoxyguanosine in oxidized DNA. Carcinogenesis 1994, 15: 2037–2043
   PubMedGoogle Scholar
• Rosen J. E., Prahalad A. K., Williams G. M. 8‐Oxodeoxyguanosine formation in the DNA of cultured cells after exposure to H2O2 alone or with UVB or UVA irradiation. Photochem. Photobiol. 1996, 64: 117–122
   PubMedGoogle Scholar
• Stollar B. D. Antibodies to DNA. CRC Crit. Rev. Biochem. 1986, 20: 1–36
   PubMedGoogle Scholar
• Stollar B. D., Zon G., Pastor R. W. A recognition site on synthetic helical oligonucleotide for monoclonal anti‐native DNA autoantibody. Proc. Natl. Acad. Sci. USA. 1986, 83: 4469–4473
   PubMedGoogle Scholar
• Tritscher A. M., Seacat A. M., Yager J. D., Miller B. D., Bell D., Sutter T. R, Lucier G. W. Increased oxidative DNA damage in livers of 2,3,7,8‐tetrachlorodibenzo‐p‐diosin treated intact but not ovariectomized rats. Cancer Lett. 1996, 98: 219–225
   PubMedGoogle Scholar
• Zouali M., Stollar B. D. Thymine and guanine base specificity of human myeloma proteins with anti‐DNA activity. Clin. Invest. 1986, 78: 1173–1178
   Google Scholar