Unmasking rogue cells in the immune system

Subduing the rebellion: Unmasking rogue cells in the immune system
Genetic alteration of a mouse embryo to "knock down" -- which is to disrupt -- the JunB gene, which is then going to be unavailable for the immune system cells to use. Credit: OIST

The immune system is a formidable defense against microbial intruders, identifying and eliminating threats through an extremely intricate and adaptable network of specialized cells. However, a system of such deep complexity is also prone to misfire. Due to genetic mutations, for example, some of these specialized immune cells can turn rogue, no longer differentiating between invaders and the body's own cells, and thus start attacking healthy tissues. For serious cases, this issue leads to autoimmune diseases such as arthritis, inflammatory bowel disease, type 1 diabetes and many more, which are widespread in the population.

Most of the current treatments against autoimmune diseases require shutting down major parts of the immune system, inhibiting desirable immune responses, and leaving the patient vulnerable to potentially life-threatening bacterial and viral infections. Such drastic solutions are required because until now, scientists had not yet fully identified a mechanism in these they could use as a selective target—the known genetic material was common between healthy and rogue cells. But in their publication in Nature Communications, researchers in Okinawa, Japan, reported a previously undiscovered role for a known molecule named JunB and its associated gene. JunB seems to be essential for a specific type of white blood cell to turn toxic.

The scientists were investigating T-helper , which coordinate the immune system response by secreting a diverse range of communication signals in the form of molecules called interleukins. JunB operates in T-helper 17 cells, a subdivision that specifically promotes the initial immune response against an infection. But sometimes, these T-helper 17 cells turn rogue and attack guts and joints.

"We have a lot of T-helper 17 cells in our guts," commented Prof. Ishikawa, author of the new study at the Okinawa Institute of Science and Technology Graduate University. "They have three major impacts on our body—first, to maintain a healthy gut, and second, to deal with bacterial and fungal infections. The third is their toxicity, leading to autoimmune diseases, which is something we want to avoid."

The OIST scientists studied the process in which T-helper 17 cells become toxic. One of the immune system communication molecules—interleukin 23—is required to activate T-helper 17 cells during an infection and make them fight the invaders. But interleukin 23 is a double-edged sword—it is also responsible for triggering the same T-helper 17 cell to turn rogue. For T-helper 17 cells to respond, they need to display interleukin 23 receptors on their surface, which means the corresponding gene—usually switched off—needs to be activated. Finding a way to stop this interleukin 23 receptor gene from being activated is potentially key to shutting down the entire process. And this is where JunB, the focus of this research, comes into play.

Subduing the rebellion: Unmasking rogue cells in the immune system
1) The normal process in which JunB can activate the Interleukin 23 (IL23) receptor gene to make the T Helper 17 cell sensitive to Interleukin 23. This potentially lead to the T Helper 17 cell to turn toxic. 2) Knocking down JunB prevents the production of Interleukin-23 receptors, and the T-Helper 17 cell cannot turn rogue any longer, but is still able to fight infections. Credit: OIST

JunB is a transcription factor, which means it regulates—switches on and/or off—the activity of a gene or a group of genes in the cell's DNA. OIST researchers from the Immune Signal Unit identified JunB by systematically checking transcription factors in the T-helper 17 cell DNA. For this purpose, they would knock down the gene DNA sequence, the for each transcription factor, one by one. For each knocked-down gene, they checked if the T-helper 17 cell still displayed its interleukin-23 receptors. When they knocked down JunB, they realized the T-helper 17 cells were no longer displaying interleukin 23 receptors and were unable to turn rogue. Moreover, mice in which T-helper cells lacked JunB were incapable of developing T-helper 17-related autoimmune diseases.

"It was quite a challenge. We knocked down around 300 transcription factors one by one," said Prof. Ishikawa. "Developing a mouse model with a knocked out JunB took us two years."

Another exciting part of this research is that T-helper 17 cells deprived of JunB are still able to accumulate in the gut and likely to cope and fight infections. Therefore, if scientists design a drug able to target JunB specifically, it should prevent T-helper 17 cells from turning rogue without impacting the immune system as a whole.

As a transcription factor, JunB activates another gene—RORγ-t—by helping three other transcription factors bind to the DNA sequence in the chromosome. The product of this gene RORγ-t is a fifth transcription factor that activates the gene Interleukin-23 receptor. Only then, the T-helper 17 cell displays interleukin 23 receptors and might turn rogue.

The scientists hope to research a future treatment against T-helper-17 related . "Previously, several such as RORγ-t have been found essential for all T-helper 17 cells," said Prof. Ishikawa. "If we use these molecules as targets for therapy, all T-helper 17 cells will be affected, toxic or not. However, JunB seems to be critical only for toxic T-helper 17 . This would allow us to develop a pinpointing, more selective therapy."


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Researchers find key mechanism to control antibody production

More information: Nature Communications (2017). DOI: 10.1038/NCOMMS15628
Journal information: Nature Communications

Citation: Unmasking rogue cells in the immune system (2017, May 30) retrieved 8 December 2019 from https://medicalxpress.com/news/2017-05-unmasking-rogue-cells-immune.html
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