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Scavenger cells accomplices to viruses

Date:
July 25, 2011
Source:
University of Zurich
Summary:
Mucosal epithelia are well-protected against pathogenic germs. However, individual viruses, such as the HI virus, still manage to enter the body via the mucous membrane somehow. Cell biologists have now identified a new infection mechanism, demonstrating that the viruses use the body’s own scavenger cells for the infection. The new findings are important for cancer-gene therapy and the development of anti-viral medication.
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Mucosal epithelia are well-protected against pathogenic germs. However, individual viruses, such as the HI virus, still manage to enter the body via the mucous membrane somehow. Cell biologists from the University of Zurich have now identified a new infection mechanism, demonstrating that the viruses use the body's own scavenger cells for the infection. The new findings are important for cancer-gene therapy and the development of anti-viral medication.

Mucosal epithelia do not have any receptors on the outer membrane for the absorption of viruses like hepatitis C, herpes, the adenovirus or polio, and are thus well-protected against pathogenic germs. However, certain viruses, such as the human immunodeficiency virus HIV, still manage to enter the body via the mucous membrane. Just how this infiltration occurs on a molecular level has been a mystery. Three hypotheses were discussed: firstly, that it's caused by mechanical damage to the mucous membrane; secondly, the presence of previously unknown receptors on the mucous membrane cells; and, thirdly, that the viruses are smuggled in via a kind of Trojan horse. Now, for the first time, cell biologists from the University of Zurich have succeeded in identifying the infection mechanism for adenoviruses.

In the recently published online magazine Nature Communications, Verena Lütschg and cell biologists from the Institute of Molecular Biology headed by Urs Greber reveal how type-5 adenoviruses in the lung epithelia utilize an immune response triggered by the infection for the progression of the infection: Adenoviruses use scavenger cells and their subsequent production of antiviral cytokines as a door-opener for the infection of the lung epithelial cells.

Exposure of shielded receptors

Antiviral cytokines play a key role in immunological reactions and trigger inflammatory responses, for instance. They induce the epithelial cells to expose certain receptors that are shielded under normal conditions and thus activate immune cells in defense. For healthy people, an infection of the lung with type-5 adenoviruses is harmless as they merely cause a cold. Under very stressful situations or in the case of chronic respiratory diseases, however, adenoviruses can cause severe, acute infections that can sometimes be fatal.

The recently identified infection mechanism can serve as a model for how the pathogens penetrate the mucosal epithelial cells and enter the body. However, it is also crucial from a therapeutic point of view. Type-5 adenoviruses are already used very often as transport vehicles in cancer-gene therapy today. Knowing the transport route will help develop both this gene therapy and specifically acting cancer treatment further.


Story Source:

Materials provided by University of Zurich. Note: Content may be edited for style and length.


Journal Reference:

  1. Verena Lütschg, Karin Boucke, Silvio Hemmi, Urs F. Greber. Chemotactic antiviral cytokines promote infectious apical entry of human adenovirus into polarized epithelial cells. Nature Communications, 2011; 2: 391 DOI: 10.1038/ncomms1391

Cite This Page:

University of Zurich. "Scavenger cells accomplices to viruses." ScienceDaily. ScienceDaily, 25 July 2011. <www.sciencedaily.com/releases/2011/07/110721102026.htm>.
University of Zurich. (2011, July 25). Scavenger cells accomplices to viruses. ScienceDaily. Retrieved April 19, 2024 from www.sciencedaily.com/releases/2011/07/110721102026.htm
University of Zurich. "Scavenger cells accomplices to viruses." ScienceDaily. www.sciencedaily.com/releases/2011/07/110721102026.htm (accessed April 19, 2024).

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