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Updated: Aug 1, 2026

An In vitro Model to Study Immune Responses of Human Peripheral Blood Mononuclear Cells to Human Respiratory Syncytial Virus Infection
Published on: December 10, 2013
[Human herpesvirus-6 infection induces IL-10 production in monocytes]
1Children's Hospital, Chongqing University of Medical Sciences, Chongqing 630014.
Insights
Interleukin 10 (IL-10) inhibits pro-inflammatory cytokine production during human herpesvirus 6 (HHV-6) infection. This suggests IL-10 plays a role in HHV-6 immune pathogenesis and latent infection.
Area of Science:
- Immunology
- Virology
- Molecular Biology
Context:
- Human herpesvirus 6 (HHV-6) is a common viral infection with complex interactions with the host immune system.
- Understanding the immune response to HHV-6 is crucial for elucidating its pathogenesis and potential for latency.
- Cytokines play a critical role in modulating immune responses during viral infections.
Purpose:
- To investigate the role of interleukin 10 (IL-10) and other cytokines in the immune pathogenesis of HHV-6 infection.
- To explore the regulatory mechanisms of cytokine production in HHV-6 infected monocytes.
- To determine the impact of endogenous IL-10 on pro-inflammatory cytokine expression during HHV-6 infection.
Summary:
- Reverse transcription-polymerase chain reaction (RT-PCR) and sandwich ELISA were used to analyze cytokine expression in HHV-6 infected monocytes.
- Results indicated that IL-10 expression increased with HHV-6 infection, while transcription of IL-1 beta, IL-6, and TNF-alpha mRNA decreased.
- Blocking endogenous IL-10 led to a significant increase in TNF-alpha, IL-1 beta, and IL-6 production, demonstrating IL-10's inhibitory role at the transcriptional level.
Impact:
- The findings suggest that endogenous IL-10 production contributes to the immune dysregulation observed in HHV-6 infection.
- IL-10's ability to suppress Th1 responses and down-regulate monocyte/macrophage function may facilitate HHV-6 latency.
- This study provides insights into the intricate interplay between HHV-6 and the host immune system, potentially informing therapeutic strategies.
Abstract:
In this report, interleukin 10(IL-10) and other cytokines were evaluated through reverse transcription-polymerase chain reaction (RT-PCR) and sandwich ELISA to explore possible immune pathogenesis of human herpesvirus 6 (HHV-6) infection. The results showed that IL-10 was expressed in HHV-6 infected monocytes. Kinetic studies found that transcription of IL-1 beta, IL-6 and TNF-alpha mRNA decreased with accumulation of IL-10 mRNA. When endogenous IL-10 induced by HHV-6 was blocked using anti-human IL-10 monoclonal antibody, the production and the expression of TNF-alpha, IL-1 beta and IL-6 markedly increased as compared with infection by HHV-6 alone, indicating that endogenous IL-10 inhibited cytokine production at the transcription level in HHV-6 infected monocytes. IL-10 has been shown to suppress Th1 response and down-regulate monocyte/macrophage function. The data from our studies suggest that disturbance of immune function and latent infection resulting from HHV-6 infection might partially contribute to endogenous IL-10 production.
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