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Amplification of autoimmune disease by infection

Reports of infection with certain chronic persistent microbes (herpesviruses or Chlamydiae) in human autoimmune diseases are consistent with the hypothesis that these microbes are reactivated in the setting of immunodeficiency and often target the site of autoimmune inflammation. New experimental an...

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Detalles Bibliográficos
Autores principales: Posnett, David N, Yarilin, Dmitry
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2005
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1065340/
https://www.ncbi.nlm.nih.gov/pubmed/15743493
http://dx.doi.org/10.1186/ar1691
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author Posnett, David N
Yarilin, Dmitry
author_facet Posnett, David N
Yarilin, Dmitry
author_sort Posnett, David N
collection PubMed
description Reports of infection with certain chronic persistent microbes (herpesviruses or Chlamydiae) in human autoimmune diseases are consistent with the hypothesis that these microbes are reactivated in the setting of immunodeficiency and often target the site of autoimmune inflammation. New experimental animal models demonstrate the principle. A herpesvirus or Chlamydia species can be used to infect mice with induced transient autoimmune diseases. This results in increased disease severity and even relapse. The evidence suggests that the organisms are specifically imported to the inflammatory sites and cause further tissue destruction, especially when the host is immunosuppressed. We review the evidence for the amplification of autoimmune inflammatory disease by microbial infection, which may be a general mechanism applicable to many human diseases. We suggest that patients with autoimmune disorders receiving immunosuppressing drugs should benefit from preventive antiviral therapy.
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spelling pubmed-10653402005-03-16 Amplification of autoimmune disease by infection Posnett, David N Yarilin, Dmitry Arthritis Res Ther Review Reports of infection with certain chronic persistent microbes (herpesviruses or Chlamydiae) in human autoimmune diseases are consistent with the hypothesis that these microbes are reactivated in the setting of immunodeficiency and often target the site of autoimmune inflammation. New experimental animal models demonstrate the principle. A herpesvirus or Chlamydia species can be used to infect mice with induced transient autoimmune diseases. This results in increased disease severity and even relapse. The evidence suggests that the organisms are specifically imported to the inflammatory sites and cause further tissue destruction, especially when the host is immunosuppressed. We review the evidence for the amplification of autoimmune inflammatory disease by microbial infection, which may be a general mechanism applicable to many human diseases. We suggest that patients with autoimmune disorders receiving immunosuppressing drugs should benefit from preventive antiviral therapy. BioMed Central 2005 2005-02-10 /pmc/articles/PMC1065340/ /pubmed/15743493 http://dx.doi.org/10.1186/ar1691 Text en Copyright © 2005 BioMed Central Ltd
spellingShingle Review
Posnett, David N
Yarilin, Dmitry
Amplification of autoimmune disease by infection
title Amplification of autoimmune disease by infection
title_full Amplification of autoimmune disease by infection
title_fullStr Amplification of autoimmune disease by infection
title_full_unstemmed Amplification of autoimmune disease by infection
title_short Amplification of autoimmune disease by infection
title_sort amplification of autoimmune disease by infection
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1065340/
https://www.ncbi.nlm.nih.gov/pubmed/15743493
http://dx.doi.org/10.1186/ar1691
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