Medical

Targeting underlying reason airways close could let asthmatics breathe easier

Targeting underlying reason airways close could let asthmatics breathe easier
A discovery by researchers at Houston Methodist Research Institute could lead to better drugs to treat asthma
A discovery by researchers at Houston Methodist Research Institute could lead to better drugs to treat asthma
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A discovery by Dr. Xian C. Li, the director of the Immunobiology & Transplant Science Center at Houston Methodist Research Institute, and his colleagues could lead to better drugs to treat asthma
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A discovery by Dr. Xian C. Li, the director of the Immunobiology & Transplant Science Center at Houston Methodist Research Institute, and his colleagues could lead to better drugs to treat asthma
A discovery by researchers at Houston Methodist Research Institute could lead to better drugs to treat asthma
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A discovery by researchers at Houston Methodist Research Institute could lead to better drugs to treat asthma

With more than 300 million people around the world estimated to suffer from asthma, and numbers increasing, scientists still don't fully understand the condition. They know that too much of a protein called mucin causes the lungs' airways to close, triggering an asthma attack, but until now, the mechanism behind this was unknown. Researchers from Houston Methodist Research Institute believe the answer lies in how two molecules communicate.

In the immune system, T helper cells help immune cells recognize and fight toxins by secreting a protein called interleukin 9 (IL-9). However, when they become hyperactive, as is the case in asthma sufferers, they secrete a molecule called OX40 that triggers the production of too much IL-9. This, in turn, results in too much mucin being produced by the mucous membranes in the airways, restricting the flow of air and causing the shortness of breath felt during an asthma attack.

"In essence, OX40 activates the IL-9 gene in T helper cells, leading to the overproduction of IL-9 through a powerful molecular machinery of super-enhancers that regulate gene expression," says Dr. Xian C. Li, the director of the Immunobiology & Transplant Science Center at Houston Methodist Research Institute.

A discovery by Dr. Xian C. Li, the director of the Immunobiology & Transplant Science Center at Houston Methodist Research Institute, and his colleagues could lead to better drugs to treat asthma
A discovery by Dr. Xian C. Li, the director of the Immunobiology & Transplant Science Center at Houston Methodist Research Institute, and his colleagues could lead to better drugs to treat asthma

Super-enhancers are regions of DNA that decide which genes become active, and by using chemical inhibitors to block those super-enhancers responsible for the hyperactivity of T helper cells, the researchers were able to prevent the overproduction of IL-9, and therefore also of mucin.

"If we can do this and develop better and more specific drugs to selectivelystop super-enhancers, asthmatic patients may never have to struggle for airagain," says Li.

The researchers are hoping they will be able to help asthma sufferers breathe easyagain by preventing the protein build-up in its beginning stages. Byunderstanding the mechanisms behind mucin buildup, their research holds thepotential for the development of a new class of drugs to treat asthma.

"Finding new approaches to target and block super-enhancers may providea new means of treatment for asthma patients that is likely to be moreefficacious than the standard of care, which is now steroids," says Li.

This study was published in the Journal of Experimental Medicine.

Source: Houston Methodist Research Institute

2 comments
2 comments
guzmanchinky
I have asthma, only around horses and cats, and haven't had an attack in decades, but I'm so glad they are developing this kind of research.
highlandboy
They need to find a better way. Deactivating T helper cell can result in immune compromised individuals. To create a choice of ways to die, immune compromised or asthma related, is not much of a choice.