Diseases & Research

Scleroderma

Hutchinson Center scientists are applying their world-class expertise in stem cell transplantation to develop treatment for Scleroderma, an autoimmune disease that attacks the skin and sometimes other body parts including joints, the digestive tract, lungs and kidneys. Our scientists made a major breakthrough when they discovered that trace fetal cells remaining in a mother's bloodstream years after pregnancy—a condition called microchimerism—are associated with the mother's development of scleroderma.

Fast Facts

  • Scleroderma is a chronic autoimmune disease, in which the body’s immune system mistakenly targets healthy cells for destruction.
  • The hallmark feature of scleroderma is hardening of the skin. Scleroderma can range from a localized disease that primarily affects the skin to a more serious illness, known as systemic sclerosis, that causes damage to multiple parts of the body, including the joints, digestive tract, lungs and kidneys.
  • Like many other autoimmune diseases, scleroderma occurs much more frequently in women than men, with about four times as many women as men developing the disease.
  • Although the cause of scleroderma is unknown, genetic and environmental factors are thought to play a role in the disease. Scleroderma does not often run in families, but there may be certain gene variants that increase likelihood of the disease.

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Prevention & Causes

Investigating scleroderma's mother-child link — Dr. J. Lee Nelson and colleagues made a major breakthrough when they discovered that trace fetal cells remaining in a mother's bloodstream years after pregnancy—a condition called microchimerism—are associated with the mother's development of scleroderma.

Nelson's team has shown that there are more fetal cells in women with scleroderma than in healthy women, and that some of the fetal cells are immune system cells. They have also found that among the cell-surface proteins that form the identification system of the immune system, molecules expressed on the cell surface—called human leukocyte antigens (HLA-DRB1)—were of particular importance. Certain relationships of these molecules on the persisting fetal cells and the mother's cells were associated with an increased risk of subsequent scleroderma in mothers studied. Learn more »

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Treatment & Prognosis

Stem-cell transplantation – Our researchers are leading clinical trials to examine the feasibility of high-dose chemotherapy and stem-cell transplantation — the standard treatment for leukemia and other blood cancers — in treating severe forms of autoimmune diseases, including multiple sclerosis and scleroderma (also known as systemic sclerosis). Their early results have been promising, prompting larger studies.

With transplantation, it may be possible to remove the reactive cells that trigger the immune system to attack the body. In such a transplantation, a patient's stem cells are collected, and cells that react against the patient's own tissue are removed. Next, the patient undergoes high-dose chemotherapy and takes drugs to suppress their immune system. The patient then receives an infusion of the stem cells that were collected before treatment, with the goal of rebuilding a new, healthier immune system. Learn more »

Mini’ transplant – Because systemic sclerosis patients do not always tolerate conventional transplants well, the Hutchinson Center is studying the effectiveness of employing a lower-intensity transplantation regimen, known as or non-myeloablative or a "mini" stem-cell transplant. This treatment, pioneered at the Hutchinson Center, involves lower doses of chemotherapy and radiation, generally reducing toxic side effects. Learn more »

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Treatment Options

Scleroderma treatment at Seattle Cancer Care Alliance

SCCA combines the expertise and experience of the Hutchinson Center, UW Medicine and Seattle Children's.

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Information about current studies involving new treatments for Scleroderma.

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