Expression of HSP-65 in Jejunal Epithelial Cells in Patients Clinically Suspected of Coeliac Disease

References

• van Eden W., van der Zee R., Paul A. G.A., Prakken B. J, Wendling U., Stephen M. A., et al. Do heat shock proteins control the balance of T-ccll regulation in inflammatory diseases?. Immunol. Today 1998; 19: 303–7
   PubMedGoogle Scholar
• Kaufmann S. H. Heat shock proteins and autoimmunity: a critical appraisal. Int. Arch. Allergy Immunol 1994; 103: 317–22
   PubMed Web of Science ®Google Scholar
• Maki M., Collin P. Coeliac disease. Lancet 1997; 349: 1755–9
   PubMed Web of Science ®Google Scholar
• Ferguson A., Arranz E., O'Mahony S. Clinical and pathological spectrum of coeliac disease - active, silent, latent, potential. Gut 1993; 34: 150–1
   PubMed Web of Science ®Google Scholar
• Arnaud-Battandier F., Cerf-Bensussan N., Amsellem R., Schmitz J. Increased HLA-DR expression by enterocytes in children with celiac disease. Gastroenterology 1986; 91: 1206–12
   PubMed Web of Science ®Google Scholar
• Savilahti E., Arato A., Verkasalo M. Intestinal gamma/delta receptor-bearing T lymphocytes in celiac disease and inflammatory bowel diseases in children. Constant increase in celiac disease. Pcdialr. Res 1990; 28: 579–81
   Google Scholar
• Halstensen T. S., Brandtzaeg P. Mucosal T cell subsets in coeliac disease: expression of T cell receptor and CD45 isoforms. Immunol. Res 1991; 10: 493–6
   PubMed Web of Science ®Google Scholar
• Holm K., Mäki M., Savilahti E., Lipsanen V., Laippala P., Koskimies S. Intraepithelial gamma/ delta T-eell-receptor lymphocytes and genetic susceptibility to coeliac disease. Lancet 1992; 339: 1500–503
   PubMed Web of Science ®Google Scholar
• Haregewoin A., Soman G., Horn R. C., Finberg R. W. Human gamma delta+ T cells respond to mycobacterial heat-shock protein. Nature 1989; 340: 309–12
   PubMed Web of Science ®Google Scholar
• O'Brien R. L, Happ M. P, Dallas A., Palmer E., Kubo R., Born W. K. Stimulation of a major subset of lymphocytes expressing T cell receptor gamma delta by an antigen derived fro. Mycobacterium tuberculosis. Cell 1989; 57: 667–74
   Google Scholar
• Hayday A. C, Roberts S., Smith A. L. γδ cells in coeliac disease. Coeliac Disease, M. Mäki, P. Collin, J. K. Visakorpi. University of Tampere, Tampere 1997; 311–20
   Google Scholar
• Cerf-Bensussan N., Cuenod-Jabri B., Guy-Grand D. Subsets of intraepithelial lymphocytes in normal intestine and in coeliac disease. Coeliac Disease, M. Mäki, P. Collin, J. K. Visakorpi. University of Tampere, Tampere 1997; 291–309
   Google Scholar
• Sollid L. M., Thorsby E. HLA susceptibility genes in celiac disease: genetic mapping and role in pathogenesis. Gastroenterology 1993; 105: 910–22
   PubMed Web of Science ®Google Scholar
• Mäki M. The humoral immune system in coeliac disease. Baillieres Clin. Gastroenterol 1995; 9: 231–49
   PubMed Web of Science ®Google Scholar
• Dieterich W., Ehnis T., Bauer M., Donner P., Volta U., Riecken E. O., et al. Identification of tissue transglutaminase as the autoantigen of celiac disease. Nature Med 1997; 3: 797–801
   PubMed Web of Science ®Google Scholar
• Sulkanen S., Halttunen T., Laurila K., Kolho K. U, Korponay-Szabo I. R, Sarnesto A., et al. Tissue transglutaminase autoantibody enzyme-linked immunosorbent assay in detecting celiac disease. Gastroenterology 1998; 115: 1322–8
   PubMed Web of Science ®Google Scholar
• Dieterich W., Laag E., Schopper H., Volta U., Ferguson A., Gillett H., et al. Autoantibodies to tissue transglutaminase as predictors of celiac disease. Gastroenterology 1998; 115: 1317–21
   PubMed Web of Science ®Google Scholar
• Picarelli A., Maiuri L., Frate A., Greco M., Auricchio S., Londei M. Production of antiendomy-sial antibodies after in-vilro gliadin challenge of small intestine biopsy samples from patients with coeliac disease. Lancet 1996; 348: 1065–7
   PubMed Web of Science ®Google Scholar
• Mäki M. Coeliac disease and autoimmunity due to unmasking of cryptic epitopes?. Lancet 1996; 348: 1046–7
   PubMed Web of Science ®Google Scholar
• Molberg O., McAdam S. N, Korner R., Quarstcn H., Kristiansen C, Madsen L., et al. Tissue transglutaminase selectively modifies gliadin peptides that are recognized by gut-derived T cells in celiac disease. Nature Med 1998; 4: 713–7
   PubMed Web of Science ®Google Scholar
• Walker-Smith J. A, Guandalini S., Schmitz J., Shmerling D. H., Visakorpi J. K. Revised criteria for diagnosis of coeliac disease. Arch. Dis. Child 1990; 65: 909–11
   PubMed Web of Science ®Google Scholar
• Halstensen T. S, Scott H., Brandlzaeg P. Intraepithelial T cells of the TcR gamma/delta+ CDS- and V delta 1/J delta 1+ phenotypes are increased in coeliac disease. Scancl. J. Immunol 1989; 30: 665–72
   PubMed Web of Science ®Google Scholar
• Spencer J., Isaacson P. G, MacDonald T. T, Thomas A. J., Walker-Smith J. A. Gamma/delta T cells and the diagnosis of coeliac disease. Clin. Exp. Immunol 1991; 85: 109–13
   PubMed Web of Science ®Google Scholar
• Iltancn S., Holm K., Partanen J., Laippala P., Mäki M. Increased density of jejunal γδ+, T cells in patients having normal mucosa marker of operative aulo-immune mechanisms?. Autoimmunity 1999; 29: 179–87
   PubMed Web of Science ®Google Scholar
• Sulkanen S., Halttunen T., Marttinen A., Leivo E. L., Laurila K., Mäki M. Autoantibodies in celiac disease: importance of fibroblasts. J. Peilialr. Gastroenterol. Nutr 1997; 27: 206–13
   Web of Science ®Google Scholar
• Ota M., Seki T., Nomura N., Sugimura K., Mizuki N., Fukushima H., et al. Modified PCR-RFLP method for HLA-DPB1 and DQAI genotyping. Tissue Antigens 1991; 38: 60–71
   PubMedGoogle Scholar
• Kimura A., Sasazuki T. Eleventh international histocompatibility workshop reference protocol for the HLA DNA-typing technique. HLA 1991, T. Sasazuki. Oxford University Press, Oxford 1992
   Google Scholar
• Wright D. K., Manos M. M. Sample preparation from paraffin-embedded tissues. PCR protocols. A Guide to Methods and Applications, M. A. Ennis. Academic Press, San Diego 1990
   Google Scholar
• Ivanyi J., Sinha S., Aston R., Cussell D., Keen M., Sengupta K. Definition of species specific and cross-reactive antigenic determinants of Mycobacterium leprae using monoclonal antibodies. Clin. Exp. Immunol 1983; 52: 528
   PubMed Web of Science ®Google Scholar
• Evans D. J, Norton P., Ivanyi J. Distribution in tissue sections of the human groEL stress-protein hotno-logue. APMIS 1990; 98: 437–41
   PubMed Web of Science ®Google Scholar
• Haregewoin A., Singh B., Gupta R. S., Finberg R. W. A mycobacterial heat-shock protein-response γδ T cell clone also responds to the homologous human heat-shock protein: a possible link between infection and autoimmunity. J Inject. Dis 1991; 163: 156–60
   PubMed Web of Science ®Google Scholar
• Groh V., Steinle A., Bauer S., Spies T. Recognition of stress-induced MHC molecules by intestinal epithelial γδ T cells. Science 1998; 279: 1737–40
   PubMed Web of Science ®Google Scholar
• Iltanen S., Holm K., Ashorn M., Ruuska T., Laippala P., Mäki M. Changing jejunal γδ TCR-bearing intraepithelial lymphocyte density in coeliac disease. Clin. Exp. Immunol 1999; 117: 515
   Web of Science ®Google Scholar
• Pujol-Bottazzo F. G, Borrell R., Hanafusa T., Feldman M. Role of aberrant HLA-DR expression and antigen presentation in the induction of endocrine autoimmunity. Lancet 1983; 2: 1115–9
   PubMed Web of Science ®Google Scholar
• Van der Zee R., Anderton S. M, Prakken A. B, Liesbeth Paul A.G., van Eden W. T cell responses to conserved bacterial heat-shock protein epitopes induce resistance in experimental autoimmunity. Semin. Immunol 1998; 10: 35–41
   PubMed Web of Science ®Google Scholar
• Res P. C.M., Schaar C. G, Breedveld F. C, van Eden W., van Embden J. D.A., Cohen I. R., et al. Synovial fluid T cell reactivity against 65 kDa a heat shock protein of mycobacteria in early chronic arthritis. Lancet 1988; 2: 478–80
   PubMed Web of Science ®Google Scholar
• Lamb J. R, Bal V., Mendez-Samperio P., Mehlert A., So A., Rothbard J. B., et al. Stress proteins may provide a link between the immune response to infection and autoimmunity. Internal. Immunol 1989; 1: 191–6
   PubMedGoogle Scholar
• Gaston J. S.H., Life P. F, Bailey L. C., Bacon P. A. In vitro responses to a 65 kilodalton mycobacterial protein by synovial T cells from inflammatory arthritis patients. J. Immunol 1989; 143: 2494–500
   PubMed Web of Science ®Google Scholar
• Bell C. G. Do stress proteins have a regulatory role in autoimmune rheumatoid arthritis. Biochem. Soc. Trans 1996; 24: 494
   Web of Science ®Google Scholar
• Prakken A. B, van Eden W., Rijkers G. T, Kuis W., de Graeff-Toebes E. A, Meeder E. R., et al. Autoreactiv-ity to human heat-shock protein 60 predicts disease remission in oligoarticular juvenile rheumatoid arthritis. Arthritis Rheumatism 1996; 39: 1826–32
   PubMed Web of Science ®Google Scholar
• Kotani T., Aratake Y., Hirai K., Hirai I., Ohtaki S. High expression of heat shock protein 60 in follicular cells of Hashimoto's thyroiditis. Autoimmunity 1996; 25: 1–8
   PubMed Web of Science ®Google Scholar
• Child D. F, Smith C. J., Williams C. P. Heat shock protein and the double insult theory for the development of insulin dependent diabetes. J. R. Soc. Med 1993; 86: 217–19
   PubMed Web of Science ®Google Scholar
• Scheinin T., Tran Minh N. N, Tuomi T., Miettinen A., Kontiainen S. Islet cell and glutamic acid decarboxylase antibodies and heat shock protein 65 responses in children with newly diagnosed insulin-dependent diabetes mellitus. Immunol. Lett 1996; 49: 123–6
   PubMed Web of Science ®Google Scholar
• Muller N., Frenzel K. H, Schwarz M., Wurl D., Hampel H., Penning R., et al. Expression of human heat-shock protein 70 antigens and gamma/delta T-cell receptor antigens in human central nervous tissue. Ann. NY Acad. Sci 1994; 741: 305–15
   PubMed Web of Science ®Google Scholar
• Freedman M. S, Bitar R., Antel J. P. Gamma/delta T-cell-human glial cell interactions. 11. Relationship between heat shock protein expression and susceptibility to cylolysis. J. Neuroimmunol 1997; 74: 143–8
   PubMed Web of Science ®Google Scholar