Attacking Flu Viruses from Two Sides

IgA1 antibodies binding to the influenza A virus antigen hemagglutinin. TSRI/UZH

Fever, shivering, headaches, and joint pains – each year millions of people around the world are affected by the flu. While most people recover after a few days, the WHO estimates that each year between 250,000 and 500,000 people die from the disease.

As there are only few effective treatment options, medical efforts have thus far focused on vaccination to combat the flu. However, since flu viruses are constantly changing, so too are the viral strains that are passed on around the globe. This means that vaccines have to be created anew each year on the basis of prognoses.

Certain antibodies provide protection in two different ways

Working together with scientists from the US, researchers at the University of Zurich have now discovered a new aspect of how the flu virus interacts with antibodies in the lungs. “This was a completely unexpected and unforeseen finding,” says Lars Hangartner, former professor at the Institute of Medical Virology of UZH. “We found that antibodies called IgAs, which are commonly found on mucosal surfaces, can actually protect us from infections in two different ways,” adds the head of the study, who now works at The Scripps Research Institute in the USA.

IgA1 antibody most effective in combatting flu viruses

Flu vaccines unfold their effects by presenting pieces of the virus – so-called antigens – to the immune system. Antigens provide the immune system with a kind of blueprint that allows it to recognize flu viruses and start the production of antibodies as soon as it encounters them again. However, current vaccines stimulate the production of another type of antibodies: Immunoglobulin G (IgG). The researchers studied different kinds of antibodies in cell cultures to find out which ones were most potent against the flu virus. They found that a subtype called IgA1, which has a special tail at one end that contains sialic acids, was the most effective.

Two-pronged attack on flu viruses

This tail blocks the part of the virus that allows it to attach to the cells it wants to infect. This suggests that the IgA1 antibody works through two different types of immune activity. Firstly, through acquired immunity, which is traditionally associated with antibodies that specifically recognize pathogens. And secondly, through innate immunity via the sialic acids at the other end of the molecule, which is more of a non-specific, broad-ranging attack. IgA antibodies thus attach themselves to flu viruses in two places at once. Hangartner was also able to demonstrate that bird flu viruses are significantly more vulnerable to such a broad-ranging attack: “It’s certainly possible that this tail is one of the reasons why we’re not that easily infected with bird flu viruses.”

Combining both advantages in one molecule

According to Hangartner, these findings could help improve the effectiveness of flu vaccinations and drugs. Since IgAs are notoriously hard to work with, the researcher believes future research should focus on developing antibodies that are easier to produce and can be tested in mice. His idea is to graft the tail of the IgA1 onto an IgG-type antibody, which is much easier to handle. “It would combine the best of both worlds and give us a molecule that’s more effective and hardy, and that ultimately may be very useful when it comes to fighting the flu,” adds the immunologist. Thanks to the strength with which the antibodies attach themselves to the virus, even small amounts would be enough to provide effective protection.

Literature:
Michael A. Maurer, Larissa Meyer, Matteo Bianchi, Hannah L. Turner, Ngoc P.L. Le, Marco Steck, Arkadiusz Wyrzucki, Vanessa Orlowski, Andrew B. Ward, Max Crispin, and Lars Hangartner. Glycosylation of human IgA directly inhibits influenza A and other sialic-acid binding viruses. Cell Reports. April 3, 2018. doi: 10.1016/j.celrep.2018.03.027

Contact:
Prof. Lars Hangartner, PhD
Department of Immunology and Microbiology
The Scripps Research Institute
La Jolla, CA, USA
Phone +1 858 784 9876
E-mail: lhangart@scripps.edu

http://www.media.uzh.ch/en/Press-Releases/2018/antibodies-attack-flu-virus.html

Media Contact

Kurt Bodenmüller Universität Zürich

All news from this category: Life Sciences

Articles and reports from the Life Sciences area deal with applied and basic research into modern biology, chemistry and human medicine.

Valuable information can be found on a range of life sciences fields including bacteriology, biochemistry, bionics, bioinformatics, biophysics, biotechnology, genetics, geobotany, human biology, marine biology, microbiology, molecular biology, cellular biology, zoology, bioinorganic chemistry, microchemistry and environmental chemistry.

Back to the Homepage

Comments (0)

Write comment

Latest posts

Researchers confront optics and data-transfer challenges with 3D-printed lens

Researchers have developed new 3D-printed microlenses with adjustable refractive indices – a property that gives them highly specialized light-focusing abilities. This advancement is poised to improve imaging, computing and communications…

Research leads to better modeling of hypersonic flow

Hypersonic flight is conventionally referred to as the ability to fly at speeds significantly faster than the speed of sound and presents an extraordinary set of technical challenges. As an…

Researchers create ingredients to produce food by 3D printing

Food engineers in Brazil and France developed gels based on modified starch for use as “ink” to make foods and novel materials by additive manufacturing. It is already possible to…

By continuing to use the site, you agree to the use of cookies. more information

The cookie settings on this website are set to "allow cookies" to give you the best browsing experience possible. If you continue to use this website without changing your cookie settings or you click "Accept" below then you are consenting to this.

Close