New Insights On Type 1 Interferons (IFN-1) For Treating Viral Infections

by Madhumathi Palaniappan on  January 12, 2017 at 2:42 PM Research News
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The ability of the immune system to neutralize a virus may depend on the expression levels of certain proteins. Type 1 interferons (IFN-1) are cytokines that contribute for antiviral response which may establish and maintain persistent viral infections.
New Insights On Type 1 Interferons (IFN-1) For Treating Viral Infections
New Insights On Type 1 Interferons (IFN-1) For Treating Viral Infections

Professor Alain Lamarre along with his team at INRS (Institut national de la recherche scientifique) - Institut Armand-Frappier Research Centre have made significant advances in understanding the role of IFN-1.

The study findings may lead to the development of novel therapeutic approaches against viral infections that are caused by the hepatitis C virus (HCV) or human immunodeficiency virus (HIV).

Multiple type I interferon signalling pathways
IFN-I is synthesized by a large number of cells and triggers diverse responses in target cells using various signalling pathways. During a typical virus infection, the virus replicates in the infected cell and induces IFN-I expression through pattern recognition receptors (PRRs) signalling. The cytokine then binds a specific receptor (IFNAR) to adjacent cells, which usually triggers reactions that stimulate the host's immune defences. However, the effect on chronic infections is different because prolonged exposure to IFN-I has negative immunomodulatory effects.

The role of IFN-I in chronic viral infections
Persistent viral infections, particularly those caused by HCV, HIV, and lymphocytic choriomeningitis virus (LCMV), an experimental model of persistent viral infections lead to a number of dysfunction to the humoral response such as an excessive production of non-specific antibodies (hypergammaglobulinemia) and a dysregulation of B cell subpopulations.

The most recent work by professor Lamarre's team has focused on the molecular mechanisms that disrupt the immune system during chronic viral infections. The study's results highlight numerous mechanisms that explain the role of IFN-I in immune response disruptions. Using specific markers, professor Lamarre's team observed an abnormal increase in the expansion of TFH (a subpopulation of CD4+ T cells), which in this case triggers the expansion of non-specific B lymphocytes. The increased amount of TFH also reduces the proportion of other T cells that help fight infection. The team has also demonstrated that IFN-I signalling affects the humoral response more directly. They have successfully restored antigen-specific responses by blocking B cell IFN-I receptors. Therefore, IFN-I acts directly on B cells to increase non-specific responses while impairing antigen-specific responses.

Professor Lamarre's team has identified the signalling pathways involved in disrupting the humoral immune response during the chronic phase of LCMV infection, but the complex responses caused by IFN-I require further characterization. While it is unclear if sustained IFN-I production is a cause or consequence of persistent viral infection, it clearly plays an important role in humoral response disruption offering a promising therapeutic target against chronic viral infections.



Source: Eurekalert

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