As part of the innate immune system natural killer cells (NK cells) play an important role in immune responses. For a long time they have been known as the first line of defense in the fight against infectious diseases. Therefore, researchers assumed that the body needs as many active NK cells as possible. However, scientists at the Helmholtz Centre for Infection Research (HZI) have now shown that the principle “the more the better” does not apply to this type of immune cells.
“During certain phases of the immune response it seems to be beneficial to have less active natural killer cells,” says Dr Jadwiga Jablonska-Koch, member of the research group “Molecular Immunology” at the HZI and responsible author of a new study published in the European Journal of Immunology. “This is particularly true during the beginning stages of an infection, which is precisely when they were assumed to be most important”.
Usually, Listeria monocytogenes infection leads to a deadly sepsis in mice and immune suppressed humans. Interestingly, researchers observed that removal of NK cells during the early stages of Listeria monocytogenes infection improves survival of the mice. These new findings could help to prevent sepsis in the future.
Until now it was believed that mice and humans die from listeriosis because their killer cells do not fight the infection effectively enough. However, the new results show the exact opposite. Even though the killer cells produce messenger substances that activate the immune system, the overproduction of the interferon IFN-γ causes problems. The large amounts of IFN-γ block the recruitment of neutrophilic granulocytes.
Those so-called scavenger cells are the most common white blood cells and are able to engulf bacteria and destroy them. If their migration to the site of infection is blocked in the initial phase, the bacteria can grow uncontrolled. This leads to fatal sepsis and death.
However, having no active NK cells could also lead to uninhibited bacteria proliferation. In later stages of an infection NK cells are crucial for the survival of both; mice and humans. “It is important to find the right balance for NK cell activity. It has to be high enough to activate other immune cells, but at the same time the migration and activation of scavenger cells shouldn’t be blocked,” says Jablonska-Koch.
Where exactly this balance lies is still not clear. At least, the scientists were able to show that in the later phases of infectious diseases it can be beneficial for the body to have large amounts of highly active NK cells. The discovery of HZI scientists could be relevant in the future, especially from a medical point of view. If these results prove to be true for humans and also for other bacteria, they could help to develop new treatment strategies. “If we know how exactly the killer cells function, we could use this information for treatment of bacterial infections. But it is still a long way to go,” says Jablonska-Koch.
Nuno Viegas, Lisa Andzinski, Ching-Fang Wu, Ronja-Melinda Komoll, Nelson Gekara,Kurt E. Dittmar, Siegfried Weiss, Jadwiga Jablonska
IFN-γ production by CD27+ NK cells exacerbates Listeria monocytogenes infection in mice by inhibiting granulocyte mobilization
European Journal of Immunology, 2013 DOI: 10.1002/eji.201242937
The focus of HZI’s Department of Molecular Immunology is to investigate the role of signaling molecules used by the immune system. One of the primary research goals is to determine how immune cells communicate with each other during an infection and which messenger substances they use for this purpose.
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