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Researchers at Duke-NUS Medical School have discovered that interleukin-11 (IL11) plays a crucial role in the aging process, associated with higher levels of fat accumulation and muscle loss—key indicators of aging. Inhibiting IL11’s effects may enhance a healthy lifespan.
An aging population is set to pose immense health, social, and economic challenges in the coming decades. As life expectancy increases, preventing the physical decline and frailty associated with aging has become a critical goal. Effective interventions in this area could lead to substantial societal and economic gains. In fact, estimates suggest that even a one-year increase in life expectancy could be valued at US$38 trillion.
In a discovery published in Nature, a team of scientists from Duke-NUS Medical School in Singapore may have found a key to slow aging.
The team demonstrated in preclinical models that the protein interleukin-11 (IL11) actively promotes aging and that giving an anti-IL11 therapy not only counteracts the deleterious effects of aging but also increases lifespan. Their discovery has the potential to play a significant role in countries’ efforts to help their population live more years in good health.
IL11 leads to fat accumulation and muscle mass loss, two key hallmarks of aging
In preclinical studies, the team found that with age, organs expressed increasing levels of the IL11 protein, which, in turn, promoted fat accumulation in the liver and abdomen, and reduced muscle mass and strength—two conditions that are hallmarks of human aging.
According to the team, these results are the first in the world to demonstrate that IL11 is a principal factor in aging.
First and co-corresponding author Assistant Professor Anissa Widjaja from Duke-NUS’ Cardiovascular and Metabolic Disorders Programme, said: “This project started back in 2017 when a collaborator of ours sent us some tissue samples for another project. Out of curiosity, I ran some experiments to check for IL11 levels. From the readings, we could clearly see that the levels of IL11 increased with age and that’s when we got really excited!”
Anti-IL11 therapy counteracts the effects of aging
After establishing IL11’s role in aging, the team demonstrated that by applying anti-IL11 therapy in the same preclinical model, metabolism was improved, shifting from generating white fat to beneficial brown fat. Brown fat breaks down blood sugar and fat molecules to help maintain body temperature and burn calories.
The researchers also observed improved muscle function and overall better health in their study, as well as an increased lifespan of up to 25 percent in both sexes.
Unlike other drugs known to inhibit specific pathways involved in aging, such as metformin and rapamycin, anti-IL11 therapy blocks multiple major signaling mechanisms that become dysfunctional with age, offering protection against multimorbidity from cardiometabolic diseases, age-related loss of muscle mass and strength as well as frailty.
In addition to these externally observable changes, anti-IL11 therapy also reduced the rate of telomere shortening and preserved mitochondria’s health and ability to generate energy.
Senior author Tanoto Foundation Professor of Cardiovascular Medicine at the SingHealth Duke-NUS Academic Medical Centre Stuart Cook, who is also with Duke-NUS’ Cardiovascular and Metabolic Disorders Programme, said:
“Our aim is that one day, anti-IL11 therapy will be used as widely as possible, so that people the world over can lead healthier lives for longer. However, this is not easy, as approval pathways for drugs to treat aging are not well-defined, and raising funds to do clinical trials in this area is very challenging.”
Prof Cook is also a Senior Consultant with the Department of Cardiology at the National Heart Centre Singapore.
Assessing the potential of the research, Professor Thomas Coffman, Dean of Duke-NUS, commented: “Despite average life expectancy increasing markedly over recent decades, there’s a notable disparity between years lived and years of healthy living, free of disease. For rapidly aging societies like Singapore’s, this discovery could be transformative, enabling older adults to prolong healthy aging, reducing frailty and risk of falls while improving cardiometabolic health.
“This latest research is a perfect example of the contributions of Duke-NUS to Singapore’s biomedical ecosystem. Across the SingHealth Duke-NUS Academic Medical Centre, our researchers and clinician-scientists conduct truly translational research, bringing discoveries from bench to bedside, benefitting people in Singapore and around the world.”
The team’s previous research on IL11’s role in the heart and kidney (published in Nature in 2017), liver (published in Gastroenterology in 2019), and lung (published in Science Translational Medicine in 2019) led to the development of an experimental anti-IL11 therapy.
Reference: “Inhibition of IL-11 signalling extends mammalian healthspan and lifespan” by Anissa A. Widjaja, Wei-Wen Lim, Sivakumar Viswanathan, Sonia Chothani, Ben Corden, Cibi Mary Dasan, Joyce Wei Ting Goh, Radiance Lim, Brijesh K. Singh, Jessie Tan, Chee Jian Pua, Sze Yun Lim, Eleonora Adami, Sebastian Schafer, Benjamin L. George, Mark Sweeney, Chen Xie, Madhulika Tripathi, Natalie A. Sims, Norbert Hübner, Enrico Petretto, Dominic J. Withers, Lena Ho, Jesus Gil, David Carling and Stuart A. Cook, 17 July 2024, Nature.
DOI: 10.1038/s41586-024-07701-9
In this latest work, the Duke-NUS team collaborated with scientists from the National Heart Centre Singapore; the MRC Laboratory of Medical Sciences in the UK; the Max Delbruck Centre for Molecular Medicine in Germany; and the University of Melbourne in Australia.
This research is supported by the Singapore Ministry of Health’s National Medical Research Council under its MOH-STaR21nov-0003 and NMRC MOH-OFIRG21nov-0006, with additional support from several other grants and philanthropic gifts.
