IL37

One-letter difference in our DNA determines whether BCG vaccine provides good protection against tuberculosis or not. Researchers have elucidated how that one letter difference affects the activation and deactivation of the immune system. The discovery not only provides more insight into interleukin-driven inflammatory responses, but also opens up new possibilities for (re)guiding the immune system. One-letter difference in our DNA determines whether BCG vaccine provides good protection against tuberculosis or not. Researchers at Radboudumc have elucidated how that one letter difference affects the activation and deactivation of the immune system. The discovery, published in Nature Genetics, not only provides more insight into interleukin-driven inflammatory responses, but also opens up new possibilities for (re)guiding the immune system. People can react very differently to the same pathogen or vaccination. One person gets sick from an invading bacterium, for instance, while another doesn't. And some vaccines work much better on some people than on others. The main reason for these individual differences lies in our genetic material, our genome. A genome differs from person to person. It is this diversity that largely determines how we react to pathogens and vaccinations. Our complete genome consists of more than 3 billion DNA molecules. In these biological DNA letters our heredity is stored. Only a small portion of these letters, about 2 percent, contain information for the proteins at work in our bodies. Those proteins are the work forces in our cells; they build us up, repair us, keep us alive. The 2 percent of the genome that codes for proteins is called the exome. It was long thought the other 98 percent of our DNA was actually redundant. It was genetic waste -- 'junk DNA' without a function. Vaccine against tuberculosis We now know that this 'junk DNA', hereafter referred to as the non-coding genome, is indeed very important. That 98 percent may not make proteins, but it can help to shape them, coordinate their production and so on. The genome does so by making pieces of RNA. Such a piece of non-coding RNA interferes with all kinds of processes in the body. Including the chance that you will (not) get sick from a pathogen. Or whether or not a vaccine will protect you properly. Let's take the BCG vaccine that protects against tuberculosis (TB) as an example. This vaccine appears to protect not only against TB, but against more infections by (epigenetic) changes that the vaccine evokes in blood-forming stem cells in the bone marrow. Different DNA letter, different immune response Among other things, those stem cells produce the white blood cells that are important in the immune system. But the BCG vaccine does not work equally well in everyone! It turns out just one letter difference in the hereditary material drives this distinction. Such a 'one letter difference' is called a single-nucleotide polymorphism, in short SNP and pronounced as 'snip'. In people with the letter G (for guanine) at this place in the genome, vaccination works very well. For people with an A (for adenine) the vaccine works only moderately. Therefore the question is: how can one letter difference have such an impact on the functioning of a person's immune system? Musa Mhlanga and Ezio Fok of Radboudumc and their colleagues tried to answer this question. Fok: "We know that a BCG vaccine activates interleukin-1β. This triggers an inflammatory process through which the immune system builds up protection against tuberculosis and other pathogens. But why does it work really well in people with a G-SNP and is it less efficient in those with an A-SNP? What exactly happens there in that molecular incubator, why do those G and A cause such a big difference in the way our immune system functions?" Director of the inflammatory process The researchers discovered that the SNP is part of a long stretch of non-coding RNA (lncRNA) they named AMANZI. AMANZI appears to be the director of interleukin-1β (IL-1β) which is at the core of the inflammatory process. After the BCG vaccine is administered, AMANZI activates IL-37 and triggers the anti-inflammatory response that regulates the activity of IL-1β. This process of regulating IL-1β is important to achieving a long-term memory of vaccination through a process called trained immunity. Prof Mihai Netea at RUMC first observed trained immunity in 2013 to be important in how vaccines like BCG are protective. "This process takes place in people with the G-SNP," says Mhlanga, "but it's less effective in people with an A-SNP. In them [A-SNP], AMANZI stably maintains the IL-37 'brake'. As a result, neither the immune responses to the vaccine and the pathogen proceed properly because IL-1β is dampened. So people with the G-SNP build up a functional defense, where in people with the A-SNP this is not the case. To check, we removed the A-SNP AMANZI variant in white blood cells. As a result we saw pro-inflammatory protection building up again, showing the effect of the one-letter difference in AMANZI once again." Epigenetics AMANZI exerts its influence by turning genes on and off, the research field of epigenetics. In the journal Nature Genetics, the researchers show in detail how long stretches of noncoding RNA (lncRNA) execute this and how small variations of just one letter affect such an epigenetic process, with profound consequences. This applies not only to AMANZI but undoubtedly to many more lncRNAs, they argue. Those variations can be neutral, but can also affect processes in the immune system negatively or positively. In this particular case, it involves an interleukin-driven inflammatory process. Mhlanga: "Several lncRNAs play a role in this process, and single-letter differences -- SNP's in other words -- may also enhance or attenuate the effect of this inflammatory process. Further research is needed to understand the combined effect of multiple polymorphisms on these IL-1β-driven immune responses. Ultimately, we want to map all components of IL-1β signaling and trained immunity in order to find out their clinical usability. Importantly, nine out of ten SNPs are in noncoding regions of the genome."

Scientists have made an important breakthrough in understanding how inflammation is regulated. They have just discovered that a key immune alarm protein previously believed to calm down the immune response actually does the opposite. Their work has numerous potential impacts, especially in the context of understanding and responding to autoimmune disorders and inflammation. Scientists from Trinity College Dublin have made an important breakthrough in understanding how inflammation is regulated. They have just discovered that a key immune alarm protein previously believed to calm down the immune response actually does the opposite. Their work has numerous potential impacts, especially in the context of understanding and responding to autoimmune disorders and inflammation. While our immune system serves a very important function protecting us from infection and injury, when immune responses become too aggressive this can lead to damaging inflammation, which occurs in conditions such as rheumatoid arthritis and psoriasis. Inflammation is triggered when our bodies produce "alarm proteins" (interleukins), which ramp up our defenses against infection and injury by switching on different components of our immune system. Understanding how and when such alarm proteins are produced and how they activate our immune system has led to major breakthroughs in the treatment of many immune conditions. Now, scientists from the Smurfit Institute of Genetics at Trinity College Dublin, led by Seamus Martin, Smurfit Professor of Genetics, have found that Interleukin-37 has an unexpected function as an immune-activating molecule, as previous studies suggested that this interleukin instead served as an "off switch" for the immune system. Professor Martin said: "Interleukins play key roles in regulating our immune systems in response to bacterial and fungal infections. However, Interleukin-37 has long remained an enigma, as it isn't found in mammals such as mice. This has presented a major obstacle to figuring out what it does as much of what we know about the human immune system has first been discovered in model organisms whose biological make-ups are similar to ours." Prior to the new study, Interleukin-37 was thought to have immune-suppressive functions but how exactly it switched off inflammation was hotly debated. However, the Trinity scientists now report that, when activated in the correct way, Interleukin-37 displays potent pro-inflammatory activity. Professor Martin added: "This pro-inflammatory impact was highly unexpected. Our work shows that the protein binds to an interleukin receptor in the skin that is known to play a key role in driving psoriasis. And, to add further intrigue to the story, this brings the total number of immune alarm molecules that signal via this particular interleukin receptor to four. "Why there are so many interleukins that bind to the same receptor is a mystery, but if we were to speculate it may be because this receptor serves a very important sentinel function in our skin, and that one alarm protein may simply not be enough to respond to the many different infectious agents that our skin encounters. Our skin is the major barrier between our bodies and the outside world that microbes must breach if they are to gain entry to our bodies and, in many respects, represents the first line of defense in our immune systems." As such, Interleukin-37 and other immune alarm proteins may have evolved to become distinct variations on the same theme that enable our bodies to detect different types of infection by becoming activated by enzymes that are distinct to each infectious agent. The research has just been published in the journal, Science Immunology, and was a collaboration between several Trinity research groups led by Professor Martin's team, which included post-doctoral scientists Dr Graeme Sullivan and Dr Pavel Davidovich, along with research groups led by Professor Ed Lavelle (School of Biochemistry and Immunology) and Professor Pat Walsh (School of Clinical Medicine).