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Published on: September 12, 2016
Amplification of autoimmune disease by infection
David N Posnett1, Dmitry Yarilin
1Immunology Program, Graduate School of Medical Sciences, Weill Medical College, Cornell University, Ithaca, NY, USA.
Abstract:
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.
Insights
Chronic persistent microbes like herpesviruses and Chlamydiae may worsen autoimmune diseases. Reactivation during immunosuppression can increase inflammation and tissue damage, suggesting preventive antiviral therapy for patients.
Area of Science:
- Immunology and Microbiology
- Autoimmune Disease Pathogenesis
- Infectious Disease Mechanisms
Background:
- Chronic persistent microbes (herpesviruses, Chlamydiae) are implicated in human autoimmune diseases.
- These microbes may reactivate during immunodeficiency, targeting sites of autoimmune inflammation.
- Existing evidence suggests a link between microbial infections and autoimmune disease exacerbation.
Purpose of the Study:
- To investigate the role of microbial reactivation in amplifying autoimmune inflammatory disease.
- To explore the potential benefits of preventive antiviral therapy in immunocompromised patients with autoimmune disorders.
Main Methods:
- Utilized experimental animal models involving mice with induced transient autoimmune diseases.
- Infected mice with specific herpesvirus or Chlamydia species to observe disease progression.
- Analyzed the impact of microbial infection on disease severity, relapse, and tissue destruction, particularly under immunosuppression.
Main Results:
- Microbial infection significantly increased the severity and induced relapse in experimental autoimmune diseases.
- Evidence indicates specific import of microbes to inflammatory sites, exacerbating tissue destruction.
- The detrimental effects were more pronounced in immunosuppressed hosts.
Conclusions:
- Microbial infection, particularly reactivation of persistent organisms, can amplify autoimmune inflammatory disease.
- This microbial-driven amplification may be a general mechanism applicable to various human autoimmune conditions.
- Preventive antiviral therapy is recommended for autoimmune patients undergoing immunosuppressive treatment.
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