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Interleukin-10 downregulates protective immunity to Brucella abortus
1Department of Microbiology, Ohio State University, Columbus 43210.
Infection and Immunity
|March 1, 1995
Summary
Neutralizing interleukin-10 (IL-10) reduced Brucella abortus bacteria in mice. This cytokine appears to suppress protective immune responses, including macrophage function and gamma interferon production.
Area of Science:
- Immunology
- Microbiology
- Infectious Diseases
Background:
- Brucella abortus is a virulent bacterium causing brucellosis.
- Interleukin-10 (IL-10) is a cytokine with known immunomodulatory functions.
- The precise role of IL-10 in B. abortus infection is not fully understood.
Purpose of the Study:
- To investigate the role of IL-10 in the host immune response to B. abortus infection.
- To determine if IL-10 influences macrophage activity and T-cell cytokine production during brucellosis.
Main Methods:
- In vivo experiments using anti-IL-10 monoclonal antibodies in infected BALB/c mice.
- In vitro studies involving neutralization of endogenous IL-10 in splenocyte cultures.
- Assessing bacterial load in spleens and gamma interferon production.
- Evaluating the effect of recombinant IL-10 on macrophage control of intracellular B. abortus.
Main Results:
- In vivo IL-10 neutralization led to a significant reduction (up to 10-fold) in splenic B. abortus.
- In vitro, neutralizing IL-10 enhanced gamma interferon production by splenocytes.
- Exogenous IL-10 impaired the ability of peritoneal macrophages to control intracellular B. abortus.
Conclusions:
- IL-10 plays a significant role in downregulating the immune response to B. abortus.
- IL-10 negatively impacts both macrophage effector functions and Th1-mediated gamma interferon production.
- Targeting IL-10 may represent a therapeutic strategy for enhancing immunity against B. abortus.