Brian Blum
April 12, 2022

Scleroderma is an autoimmune disease characterized by a hard, inflexible layer of skin on the arms, legs and face. In about a third of the cases, the disease, which mainly strikes women aged 30 to 50, spreads beyond the extremities and damages internal organs.

“Scleroderma is one of the most frustrating disorders to treat – we can alleviate some of the patient’s symptoms, but usually we cannot significantly affect the cause of the disease, block its progression or reverse its course,” explained Dr. Chamutal Gur, a senior rheumatologist at Hadassah-Hebrew University Medical Center in Jerusalem.

So, Gur and colleagues in Prof. Ido Amit’s immunology research lab at the Weizmann Institute of Science in Rehovot set out to find the root of this dangerous affliction.

The researchers collected skin samples from nearly 100 scleroderma patients and more than 50 healthy volunteers, making this the largest study of its kind. Gur, who has skin in the game, so to speak (two of her cousins have scleroderma), performed nearly 20 skin biopsies on herself.

While searching for expected differences in immune cell function between the scleroderma patients and the control group, the researchers instead discovered differences in the fibroblasts –supporting cells considered uniform “background players” holding cells in place.

The study, published in the medical journal Cell, reveals that fibroblasts actually perform various vital functions, from conveying immune system signals to affecting metabolism, blood clotting and blood vessel formation.

The Israeli researchers discovered one a subset of fibroblasts whose concentration drops sharply in the early stages of scleroderma. Gur and her team named these cells scleroderma-associated fibroblasts, abbreviated as ScAFs.

In healthy skin (left), ScAFs feature long, thin extensions (green). In patients with limited scleroderma (center), and in those with diffuse scleroderma (right), the numbers of ScAFs are reduced. They gradually lose their elongated extensions and develop altered expression levels of certain proteins (blue, red). Image courtesy of Weizmann Institute of Science

In the healthy control group, ScAFs accounted for nearly 30 percent of all fibroblasts. In the scleroderma patients, this percentage was dramatically lower and continued to plummet as the disease progressed.

The researchers tapped these cells’ RNA to determine what transforms a functional ScAF into the kind of malfunctioning cell common in scleroderma. They also identified biological markers correlated with specific kinds of organ damage.

These markers could lead to the development of personalized treatments to prevent life-threatening complications of scleroderma.

“The reduction in the size of a critical subset of fibroblasts appears to be an early event in the course of scleroderma,” Amit noted. “It might be possible to design a therapy that will make up for this loss, slowing the progression of the disease.”

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