Chinese scientists have developed a clock that can track immune aging in humans

Source Cryptopolitan

New study by Chinese scientists has shed more light on how humans age, particularly the immune system. More interestingly, they found a way to slow down the process.

The immune cells are a key part of the body that keep humans healthy. But that also means when the cells age, the body grows weaker, and aging accelerates. The scientists specifically noted that the aging of the immune system is what drives organismal aging.

But for a long time, measuring immune aging in humans or even identifying druggable targets to fix has been difficult due to the diverse cell types and the complexity of the system as a whole. Traditional methods relied on single biomarkers that rarely paint an accurate picture of the immune system. 

That’s the hard nut Chinese scientists just cracked, according to a study report published in Immunity this week.

Chinese scientists develop a clock that tracks immune aging

The scientists were able to create a so-called Human Immune Aging Clock (HIAC) that could precisely map immune aging. 

HIAC was constructed from a single-cell multi-omics dataset of nearly 1.2 million human peripheral blood mononuclear cells collected from 230 individuals, with ages ranging from 60 years.

Graphical abstract of the study. Source: Immunity
Graphical abstract of the study. Source: Immunity

The study also led to an important discovery that the immune cells hit an inflection point around age 40, from where they quickly begin to remodel and age. It also identified T cell transcriptomes as the key indicators of immune aging. As the immune system ages, the proportion of naive T cells tends to decline as well. 

The scientist found that people with decelerated immune aging had high proportions of T  cells and exhibited more youthfulness. 

RUNX1 spotted as a factor that can slow immune aging

The study identified RUNX1 as a central regulator, key to slowing down immune aging in humans. RUNX1 is one particular transcription factor that keeps T cells youthful. However, its expression in the T cells was found to decline with age. 

The scientists discovered that when RUNX1 is removed from young T cells, they began to show signs of aging. However, it was restored in aged T cells, and those signs were alleviated, enabling the cells to maintain their youthfulness. Animal studies have already proven successful. 

“Our study provides a quantitative tool for assessing immunosenescence and nominates RUNX1 as a target for rejuvenating aged immunity,” the scientists wrote in the report.

The exciting summary of the study would be that, by restoring RUNX1, aged T cells will function more like younger ones. In turn, that will help decelerate immune aging and potentially the overall body aging process. 

The study marks yet another progress in longevity research. Earlier this month, Cryptopolitan reported another big event, with scientists at Life Biosciences planning to begin the first trial of partial reprogramming in humans. The trial begins later this year, treating up to 12 people with glaucoma, via a therapy based on three Yamanaka factors, excluding c-Myc.

The therapy already worked well in animal studies, with the scientists successfully restoring eye cells in mice back to a younger state.

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