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Published on: February 18, 2015
Cytokine involvement in immunomodulatory activity affected by Candida albicans mannan
1Department of Microbiology and Immunology, Tulane University Medical School, New Orleans, Louisiana 70112-2699, USA.
Insights
Candida albicans mannoprotein (MAN) downregulates delayed hypersensitivity (DH) by inducing CD8+ effector cells. Cytokines like IL-10, IL-4, and IFN-gamma play a role in this MAN-induced immune suppression.
Area of Science:
- Immunology
- Cellular and Molecular Immunology
Background:
- Candida albicans mannoprotein (MAN) is known to induce CD8+ effector cells.
- These cells can suppress delayed hypersensitivity (DH) responses in immunized hosts.
Purpose of the Study:
- To investigate the role of cytokines in the induction and elicitation of MAN-induced DH downregulation.
- To elucidate the mechanisms by which MAN-activated cells lead to immune suppression.
Main Methods:
- Qualitative and quantitative analysis of splenic mRNA for cytokines (IL-2, IL-4, IL-10, IL-12p40, IFN-gamma).
- Measurement of serum IL-12p40 and IL-12p70 levels.
- In vivo administration of anti-IL-4 to assess its effect on MAN-induced DH.
Main Results:
- IL-12p40 mRNA expression initially decreased then rebounded; IL-10 transcripts were consistently present.
- IL-4 and IFN-gamma mRNA were detected later in the time course.
- Anti-IL-4 treatment partially blocked DH downregulation when administered concurrently with MAN.
Conclusions:
- MAN-induced downregulation of DH involves complex cytokine interactions, including IL-10, IL-4, and IFN-gamma.
- The findings suggest that MAN-activated cells, in conjunction with specific cytokines and potentially low IL-12 activity, generate CD8+ downregulatory cells.
- IL-12p40 may contribute to the antagonistic effects observed in DH modulation.
Abstract:
Candida albicans mannoprotein (MAN) administered intravenously to mice stimulates the production of splenic CD8+ effector cells which downregulate delayed hypersensitivity (DH) in immunized mice. Cytokine involvement in the induction and/or elicitation of downregulation was studied by (i) examining murine splenocytes qualitatively for mRNA for interleukin-2 (IL-2), IL-4, IL-10, IL-12p40, and gamma interferon (IFN-gamma), (ii) quantitating splenocyte mRNA for IL-12p40 by quantitative-competitive reverse transcriptase-mediated PCR, and (iii) measuring serum levels of IL-12p40 and IL-12p70 by capture enzyme-linked immunosorbent assay, each performed at selected intervals over 96 h after giving MAN. Further, the effect of in vivo administration of anti-IL-4 on the induction and elicitation of MAN-specific DH in MAN-treated mice was measured. Expression of IL-12p40 mRNA in the spleen was reduced to near 0 during the first 24 h but rebounded thereafter. Transcripts for IL-10 were present throughout the 96-h period, whereas those for IL-4 and IFN-gamma were either weak or undetectable prior to 24 to 48 h. In vivo administration of anti-IL-4 partially abrogated the downregulatory effect of MAN only when given at the time of MAN administration. Serum levels of IL-12p40, but not IL-12p70, were increased by 24 h and maximal at 48 h. The antagonistic effect of IL-12p40 could contribute to the mechanism(s) for downregulation of DH. Moreover, IL-10, IL-4, and/or IFN-gamma, interacting with MAN-activated cells in the absence of biologically active IL-12, may induce the production of CD8+ downregulatory effector cells. Partial abrogation of downregulatory activity in animals treated with anti-IL-4 at the time of induction of such activity lends support to this hypothesis.
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