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Acta Clinica Belgica
International Journal of Clinical and Laboratory Medicine
Volume 50, 1995 - Issue 3
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Editorial

Heat-Shock Proteins in Medicine

Pages 131-136 | Published online: 16 May 2016

References

  • Young RA. Stress proteins and immunology. Annu Rev Immunol. 1990; 8: 401–20.
  • Jindal S, Dudani AK, Singh B, Harley CB, Gupta RS. Primary structure of a human mitochondrial protein homologous to the bactcrial and plant chapcronins and to the 65-Kilodalton mycobacterial antigen. Mol Cell Biol. 1989; 9: 2279–83.
  • Kaufmann SHE. Heat shock proteins and the immune response. Immunology Today. 1990; 11: 129–36.
  • Martin J, Horwich AL, Hartl FU. Prevention of protein denaturation under heat stress by the chaperonin Hsp60. Science. 1992; 258: 995–8.
  • KogaT, Wand-WUrttenbergcr A, DeBruyn J, Munk ME, Schoel B, Kaufmann SHE. T cells against a bacterial heat shock protein recognize stressed macrophages. Science. 1989; 245: 1112–15.
  • Anderton SM, van der Zee R, Goodacre JA. Inflammation activates self hsp60-specific T cells. Eur J Immunol. 1993; 23:33–8.
  • Haregewoin A, Singh B, Gupta RS, Finberg RW. A mycobacterial heat-shock protein-responsive 78 T cell clone also responds to the homologous human heat-shock protein: a possible link between infection and autoimmunity. J Infect Dis. 1991; 163: 156–60.
  • Ferm MT, SOderstrOm K, Jindal S et al. Induction of human hsp60 expression in monocytic cell lines. Int Immunol. 1992; 4: 305–11.
  • Friedland JS, Shattock R, Remick DG, Griffin E. Mycobacterial 65-kD heat shock protein induces release of proinflammatory cytokines from human monocytic cells. Clin Exp Immunol. 1993; 91:5862.
  • Pectermans WE, Raats CJI, Langermans JAM, van Furth R. Mycobacterial heat-shock protein 65 induces proinflammatory cytokines but does not activate human mononuclear phagocytes. ScandJ Immunol 1994; 39: 613–7.
  • Peetermans WE, Raats CJI, van Furth R, Langermans J’AM. Mycobacterial 65 kDa heat-shock protein induces TNF-a and IL-6, reactive nitrogen intermediates and toxoplasmastatic activity in murine peritoneal macrophages. Submittted for publication.
  • Verdegaal EME, Zegvcld ST. van Furth R. Heatshock protein 65 induces E-selectin, VCAM-1 and ICAM-1 on cultured endothelial cells and increases their adhesiveness for monocytes and granulocytes. Submitted for publication.
  • Del Giudice G. Gervaix A, Costantino Petal. Priming to heat-shock proteins in infants vaccinated against pertussis. J Immunol. 1993; 150:2025–32.
  • Hogervorst EJM, Wagenaar JPA, Boog CJP, van der Zee R, van Embden JDA, van Eden W. Adjuvant arthritis and immunity to the mycobacterial 65 kDa heat shock protein. Int Immunol. 1992; 4: 719–27.
  • van Eden W. Heat-shock proteins as immunogenic bactcrial antigens with the potential to indiitc and regulate autoimmune arthritis. Immunol Rev. 1991; 121:5–28.
  • Res PCM, Schaar CG, Breedveld FC et al. Synovial fluid T cell reactivity against 65 kD heat shock protein of mycobacteria in early chronic arthritis. Lancet. 1988; ii: 478–82.
  • Karlsson-Parra A, SOderstrOm K, Ferm M, Ivanyi J, Kiessling R, Klareskog L. Presence of human 65 kD heat shock protein (hsp) in inflamed joints and subcutaneous nodules of RA patients. Scand J Immunol. 1990;31:283–8.
  • Tsoulfa G, Rook GAW, van Embden JDA et al. Raised scrum IgG and IgA antibodies to mycobacterial antigens in rheumatoid arthritis. Ann Rheum Dis. 1989; 48: 118–23.
  • de Graeff-Meeder ER, van der Zee R, Rijkers GT et al. Recognition of human 60 kD heat shock protein by mononuclear cells from patients with juvenile chronic arthritis. Lancet. 1991; 337:1368–72.
  • Hermann E, Lohse AW, van der Zee R et al. Synovial fluid-derived Yersinia-reactive T cells responding to human 65-kDa heat-shock protein and heat-stressed antigen-presenting cells. Eur J Immunol. 1991;21:2139–43.
  • Boog CJP, de Graeff-Meeder ER, Lucassen M A et al. Two monoclonal antibodies generated against human hsp60 show reactivity with synovial membranes of patients with juvenile chronic arthritis. J Exp Med. 1992; 175: 1805–10.
  • Hcrmon-Taylor J. Causation of Crohn’s disease: the impact of clusters. Gastroenterology. 1993; 104: 643–6.
  • Wakefield AJ, Ekbom A, Dhillon AP, Pitlilo RM, Pounder RE. Crohn’s disease: pathogenesis and persistent measles virus infection. Gastroenterology. 1995; 108: 911–6.
  • Mayer L, Eiscnhardt D. Lack of induction of suppressor T cells by intestinal epithelial cells from patients with inflammatory bowel disease. J Clin Invest. 1990; 86: 1255–60.
  • Rutgecrts P, Geboes K, Pecters M el al. Effect of faecal stream diversion on recurrence of Crohn’s disease in the neoterminal ileum. Lancet. 1991; 338:771–4.
  • Sartor RB, Bond TM, Schwab JH. Systemic uptake and intestinal inflammatory effect of luminal bacterial cell wall polymers in rats with acute colonic injury. Infect Immun. 1988; 56: 2101–08.
  • Pinter U, Schonhaar A, Fleischer B, Hermann E, Meyer zum Biischcnfclde KH. Reactivity of infiltrating T lymphocytes with microbial antigens in Crohn’s disease. Lancet. 1991; 338: 1238–39.
  • Peetcrmans WE. Cellular and humoral immune response to the 65 kDa heat-shock protein in Crohn’s disease. In: Heat-shock protein 65 stimulates mononuclear phagocytes, (thesis). Lcuven, Acco 1994; 93–104.
  • Peetcrmans WE, D’Haens GR, Ceuppens JL, Rutgecrts P, Geboes K. Mucosal expression by B7-positive cells of the 60-kilodalton heat-shock protein in inflammatory bowel disease. Gastroenterology 1995; 108: 75–82.
  • Linsley PS, Lcdbetter JA. The role of the CD28 receptor during T cell responses to antigen. Annu Rev Immunol. 1993; 11: 191–212.
  • Wick G, Schett G, Amberger A, Kleindienst R, Xu Q. Is atherosclerosis an immunologically mediated disease? Immunol Today. 1995; 16: 27–33.
  • Xu Q, Dietrich H, Steiner HJ et al. Induction or arteriosclerosis in normocholcstcrolemic rabbits by immunization with heat shock protein 65. Arterioscler Thromb. 1992; 12: 789–99.
  • Xu Q, Kleindienst R, Waitz W et al. Increased expression of heat-shock protein 65 coincides with a population of infiltrating T-lymphocyles in atherosclerotic lesions of rabbits specifically responding to heat-shock protein 65. J Clin Invest. 1993; 91 2693–702.
  • Xu Q, Willeit H, Marosi M et al. Association of scrum antibodies to heat-shock protein 65 with carotid atherosclerosis. Lancet. 1993: 341: 255–9.
  • Saikku P, Lcinoncn M, Tenkanen L et al. Chronic Chlamydia pneumoniae infection as a risk for coronary heart disease in the Helsinki heart study Ann Intern Med. 1992; 116: 273–8.

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