Identification of heat shock proteins binding to an immunodominant uveitopathogenic peptide of IRBP

References

• Gery I., Wiggert B., Redmond T. M., Kuwabara T., Crawford M. A., Vistica B. P., Chader G. J. Uveoretinitis and pinealitis induced by immunization with interphotoreceptor retinoid-binding protein. Invest. Ophthalmol. Vis. Sci. 1986; 27: 1296–1300
   PubMed Web of Science ®Google Scholar
• Nussenblatt R. B., Gery I., Wacker W. B. Experimental autoimmune uveitis: cellular immune responsiveness. Invest. Ophthalmol. Vis. Sci. 1980; 19: 686–690
   PubMed Web of Science ®Google Scholar
• Chan C. C., Mochizuki M., Palestine A., Ben Ezra D., Gery I., Nussenblatt R. B. Kinetics of T lymphocyte subsets in the eye of lewis rats with experimental autoimmune uveitis. Cell Immunol. 1985; 96: 430–434
   PubMed Web of Science ®Google Scholar
• Gery I., Mochizuki M., Nussenblatt R. B. Retinal specific antigen and immunopathogenic processes they provoke. Progress and Retinal Research, N. Osborne, G. J. Chader. Pergamon Press, OxfordEngland 1986; 75–109
   Google Scholar
• Nussenblatt R. B., Palestine A. G. Uveitis: Fundamentals and clinical practice. Year Book Medical Publishers, Chicago 1989
   Google Scholar
• Nussenblatt R. B., Kuwabara T., DeMonasterio F. M., Wacker W. B. S-antigen uveitis in primates: A new model for human disease. Arch. Ophthalmol. 1981; 99: 1090–1092
   PubMedGoogle Scholar
• Nussenblatt R. B., Mittal K. K., Ryan S., Green W. R., Maumenee A. E. Birdshot retinochoroidopathy associated with HLA-A29 antigen and immune responsiveness to retinal S-antigen. Am. J. Ophthalmol. 1982; 94: 147–158
   PubMed Web of Science ®Google Scholar
• Faure J. P. Autoimmunity and the retina. Curr. Top. Eye Res. 1980; 2: 215–302
   PubMedGoogle Scholar
• Wacker W. B., Donoso L. A., Kalsow C. M., Yankeelov J. A., Jr, Organisciak D. T. Experimental allergic uveitis. Isolation, characterization and localization of a soluble uveitopathogenic antigen from bovine retina. J. Immunol. 1977; 119: 149–158
   PubMed Web of Science ®Google Scholar
• Mochizuki M., Kuwabara T., McAllister C., Nussenblatt R. B., Gery I. Adoptive transfer of experimental autoimmune uveoretinitis in rats. Invest. Ophthalmol. Vis. Sci. 1985; 26: 1–9
   PubMed Web of Science ®Google Scholar
• Rozenszajn L. A., Muellenberg-Coulombre C., Gery I., Saied M. EL., Kuwabara T., Mochizuki M., Lando Z., Nussenblatt R. B. Induction of experimental autoimmune uveoretinitis (EAU) in rats by T lines. Immunology 1986; 57: 559
   PubMed Web of Science ®Google Scholar
• Caspi R. R., Roberge F. G., McAllister C. G., El-Saied M., Kuwabara T., Gery I., Hanna E., Nussenblatt R. B. T cell lines mediating experimental autoimmune uveoretinitis (EAU) in the rat. J. Immunol. 1986; 136: 928–933
   PubMed Web of Science ®Google Scholar
• Chain B. M., Kaye P. M., Shaw M. A. The biochemistry and cell biology of antigen processing. Immunol. Rev. 1988; 106: 33–58
   PubMed Web of Science ®Google Scholar
• Unanue E. R., Allen P. M. The basis for the immunoregulatory role of macrophages and other accessory cells. Science 1987; 236: 551–557
   PubMed Web of Science ®Google Scholar
• Unanue E. R., Cerottini J. C. Antigen presentation. FASEB J. 1989; 3: 2496–2502
   PubMed Web of Science ®Google Scholar
• Marsh E. W., Dalke D. P., Pierce S. K. Biochemical evidence for the rapid assembly and disassembly of processed antigen-major histocompatibility complex class II complexes in acidic vesicles of B cells. J. Exp. Med. 1992; 175: 425–436
   PubMed Web of Science ®Google Scholar
• Harding C. V., Roof R. W., Unanue E. R. Turnover of Ia-peptide complexes is facilitated in viable antigen-presenting cells: biosynthetic turnover of Ia vs. peptide exchange. Proc. Natl. Acad. Sci. USA. 1989; 1989: 4230–4234
   Google Scholar
• Davidson H. W., Reid P. A., Lanzavecchia A., Watts C. Processed antigen binds to newly synthesized class II molecules in antigen-specific B lymphocytes. Cell 1991; 67: 105–116
   PubMed Web of Science ®Google Scholar
• Lakey E. K., Casten L. A., Niebling W. L., Margoliash E., Pierce S. K. Time dependence of B cell processing and presentation of peptide and native protein antigens. J. Immunol 1988; 140: 3309–3314
   PubMed Web of Science ®Google Scholar
• Ellis R. J. The molecular chaperone concept. Semin. Cell Biol. 1990; 1: 1–9
   PubMedGoogle Scholar
• Lakey E. K., Margoliash E., Pierce S. K. Identification of a peptide binding protein that plays a role in antigen presentation. Proc. Natl. Acad. Sci. USA. 1987; 84: 1659–1693
   PubMed Web of Science ®Google Scholar
• Flynn G. C., Pohl J., Flocco M. T., Rothman J. E. Peptide-binding specificity of the molecular chaperone BiP. Nature 1991; 353: 726–730
   PubMed Web of Science ®Google Scholar
• Flajnik M. F., Canel C., Kramer J., Kasahara M. Evolution of the major histocompatibiliry complex: molecular cloning of major histocompatibility complex class I from the amphibian Xenopus. Proc. Natl. Acad. Sci. USA. 1991; 88: 537–541
   PubMed Web of Science ®Google Scholar
• de Smet M. D., Yamamoto J. H., Mochizuki M., Gery I., Singh V. K., Shinohara T., Wiggert B., Chader G. J., Nussenblat R. B. Cellular immune responses of patients with uveitis to retinal antigens and their fragments. Am. J. Ophthalmol. 1990; 110: 135–142
   PubMed Web of Science ®Google Scholar
• Borst D. E., Redmond T. R., Elser I. E., Gonda M. A., Wiggert B., Chader G. J., Nickerson J. M. Inter-photoreceptor retinoid binding protein-gene characterization, protein repeat structure, and its evolution. J Biol. Chem. 1989; 264: 1115–1123
   PubMed Web of Science ®Google Scholar
• Beckmann R. P., Lovett M., Welch W. J. Examiming the function and regulation of hsp 70 in cells subjected to metabolic stress. J. Cell Biol. 1992; 117: 1137–1150
   PubMed Web of Science ®Google Scholar
• Ghassemi M., Heydari A. R., Richardson A. Induction of heat shock proteins inlymphocytes increases with mitogen stimulation. Immunol. Lett. 1991; 30: 333–338
   PubMed Web of Science ®Google Scholar
• Gontijo C. M., Möller G. Antigen processing and presentation by small and large B cells. Scand. J. Immunol. 1991; 34: 207–213
   PubMed Web of Science ®Google Scholar
• Hu L. H., Redmond T. M., Sanui H., Kuwabara T., McAllister C. C., Wiggert B., Chader G. J., Gery I. Rat T-cell lines specific to a nonimmunodominant deterimant of a retinal protein (IRBP) produce uveoretinitis and pinealities. Cell Immunol. 1989; 122: 251–261
   PubMed Web of Science ®Google Scholar
• Pierce S. K., Morris J. F., Grusby M. J., Kaumaya P., Van Buskirk A., Srinivasan M., Crump B., Smolenski L. A. Antigen-presenting function of B lymphocytes. Immunolog. Rev. 1988; 106: 149–180
   PubMed Web of Science ®Google Scholar
• Guillet J. G., Lai M. Z., Briner T. J., Buus S., Sette A., Grey H. M., Smith J. A., Gefter M. L. Immunological self, nonself discrimination. Science 1987; 235: 865–870
   PubMed Web of Science ®Google Scholar
• Sanui H., Redmond T. M., Kotake S., Wiggert B., Hu L.-H., Margalit H., Berzofsky J. A., Chader G. J., Gery I. Identification of an immunodominant and highly immunopathogenic determinant in the retinal interphotoreceptor retinoid-binding protein (IRBP). J. Exp. Med. 1989; 169: 1947–1960
   PubMed Web of Science ®Google Scholar
• Lindquist S. The heat shock response. Annu. Rev. Biochem. 1986; 55: 1151–1191
   PubMed Web of Science ®Google Scholar
• Heine L., Drabent B., Benecke B. J., Gunther E. A novel monoclonal antibody directed against the heat-inducible 68 kDa heat shock protein. Hybridoma 1991; 10: 721–730
   PubMedGoogle Scholar
• Minota S., Cameron B., Welch W. J., Winfield J. B. Autoantibodies to the constitutive 73-kD member of the lisp 70 hamily of heat shock proteins in systemic lupus erythematosus. J. Exp. Med. 1988; 168: 1475–1480
   PubMed Web of Science ®Google Scholar
• Milarski K. L., Welch J. W., Morimoto R. I. Cell cycle-dependent association of hsp 70 with specific cellular proteins. J. Cell Biol 1989; 96: 286–290
   Google Scholar
• Young R. A. Stress proteins and immunology. Annu Rev Immunol. 1990; 8: 401–420
   PubMed Web of Science ®Google Scholar
• Spector N. L., Freedman A. S., Freeman G., Segil J., Whitman J. F., Welch W. J., Nadler L. M. Activation primes human B lymphocytes to respond to heat shock. J. Exp. Med. 1989; 170: 1763–1768
   PubMed Web of Science ®Google Scholar
• Haire R. N., Peterson M. S., O'Leary J. J. Mitogen activation induces the enhanced synthesis of two heat-shock proteins in human lymphocytes. J. Cell Biol. 1988; 106: 883–891
   PubMed Web of Science ®Google Scholar
• Young D. B. Heat-shock proteins: immunity and autoimmunity. Curr. Opin. Immunol. 1992; 4: 396–400
   PubMed Web of Science ®Google Scholar