Literature DB >> 9353151

Experimental immunization with anti-rheumatic bacterial extract OM-89 induces T cell responses to heat shock protein (hsp)60 and hsp70; modulation of peripheral immunological tolerance as its possible mode of action in the treatment of rheumatoid arthritis (RA).

A Bloemendal1, R Van der Zee, V P Rutten, P J van Kooten, J C Farine, W van Eden.   

Abstract

OM-89 is a bacterial (Escherichia coli) extract used for oral administration in the treatment of RA. Given the evidence that immunity to bacterial heat shock antigens plays a critical role in the immunomodulation of arthritis and possibly inflammation in general, the purpose of the present studies was to evaluate the presence and immunogenicity of hsp in OM-89. Furthermore, we studied the effects of OM-89 in an experimental arthritis, where hsp are known to have a critical significance in disease development. In rats immunization with OM-89 was found to lead to proliferative T cell responses to hsp60 and hsp70 of both E. coli and mycobacterial origin. Conversely, immunization with hsp antigens was also found to induce T cell reactivity specific for OM-89. Based on this and the antigen specificity analysis of specific T cell lines, hsp70(DnaK) turned out to be one of the major immunogenic constituents of OM-89. Parenteral immunization with OM-89 was found to reduce resistance to adjuvant arthritis (AA), whereas oral administration was found to protect against AA. Given the arthritis-inhibitory effect of oral OM-89 in AA, it is possible that peripheral tolerance is induced at the level of regulatory T cells with specificity for hsp. This may also constitute a mode of action for OM-89 as an arthritis-suppressive oral drug.

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Year:  1997        PMID: 9353151      PMCID: PMC1904786          DOI: 10.1046/j.1365-2249.1997.4841378.x

Source DB:  PubMed          Journal:  Clin Exp Immunol        ISSN: 0009-9104            Impact factor:   4.330


  6 in total

Review 1.  Treating arthritis by immunomodulation: is there a role for regulatory T cells?

Authors:  Ellen J Wehrens; Femke van Wijk; Sarah T Roord; Salvatore Albani; Berent J Prakken
Journal:  Rheumatology (Oxford)       Date:  2010-05-12       Impact factor: 7.580

Review 2.  Arthritis protective regulatory potential of self-heat shock protein cross-reactive T cells.

Authors:  W van Eden; U Wendling; L Paul; B Prakken; P van Kooten; R van der Zee
Journal:  Cell Stress Chaperones       Date:  2000-11       Impact factor: 3.667

Review 3.  The involvement of heat-shock proteins in the pathogenesis of autoimmune arthritis: a critical appraisal.

Authors:  Min-Nung Huang; Hua Yu; Kamal D Moudgil
Journal:  Semin Arthritis Rheum       Date:  2009-12-06       Impact factor: 5.532

4.  Treatment of experimental adjuvant arthritis with the combination of methotrexate and lyophilized Enterococcus faecium enriched with organic selenium.

Authors:  J Rovenský; K Svík; M Stancíková; R Istok; L Ebringer; M Ferencík
Journal:  Folia Microbiol (Praha)       Date:  2002       Impact factor: 2.099

Review 5.  Immunity to heat shock proteins and arthritic disorders.

Authors:  W van Eden
Journal:  Infect Dis Obstet Gynecol       Date:  1999

Review 6.  Heat shock proteins (HSPs) in the homeostasis of regulatory T cells (Tregs).

Authors:  Tomasz Koliński; Natalia Marek-Trzonkowska; Piotr Trzonkowski; Janusz Siebert
Journal:  Cent Eur J Immunol       Date:  2016-10-25       Impact factor: 2.085

  6 in total

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