Scientists have found a new therapy for the severe inflammatory skin disorder.
A version of this article was originally published on HCPLive® by editor, Lana Pine. This version has been lightly edited.
Scientists affiliated with the National Institutes of Health (NIH) and their colleagues have identified a potential treatment option for disabling pansclerotic morphea (DPM).
DPM is a rare systemic inflammatory skin disorder associated with poor wound healing, squamous cell carcinoma, high rates of mortality, and more. There is currently no associated cause, and it the most rare form of morphea. Due to poor wound healing, patients’ skin and muscles become deeply scarred. When their muscles harden, their joints stiffen and begin to limit mobility.1
According to a press release from the NIH,1 researchers from the National Human Genome Research Institute (NHGRI); University of California, San Diego; University of Pittsburgh; National Institute of Arthritis and Musculoskeletal and Skin Diseases; and the National Institute of Allergy and Infectious Diseases collaborated in an investigative study2 related to the condition.
In the study, researchers evaluated 4 patients with DPM, all of whom had an autosomal dominant pattern of inheritance. They conducted genomic sequencing, primary skin fibroblast and cell-line assays, and gene expression. They discovered that all 4 patients with the disease had overreactive signal transducer and activator of transcription 4 (STAT4) proteins.
Additional analyses revealed the following discoveries:
“Researchers previously thought that this disorder was caused by the immune system attacking the skin,” said Sarah Blackstone, a predoctoral fellow within NHGRI's Inflammatory Disease Section, a medical student at the University of South Dakota, and co–first author of the study, in the press release. “However, we found that this is an oversimplification and that both skin and the immune system play an active role in disabling pansclerotic morphea.”
The researchers said they hope to continue studying molecules within this pathway in order to make further advancements for patients with DPM and related conditions. Dan Kastner, MD, PhD, is an NIH distinguished investigator, head of NHGRI’s Inflammatory Disease Section, and a senior author of the study, and he said these results play a role in the future of treating patients with wound healing and scarring conditions.
“The findings of this study open doors for JAK inhibitors to be a potential treatment for other inflammatory skin disorders or disorders related to tissue scarring, whether it is scarring of the lungs, liver or bone marrow,” he said.
References
1. NIH scientists find treatment for rare genetic skin disorder. News release. National Institutes of Health. May 31, 2023. Accessed June 1, 2023. https://www.nih.gov/news-events/news-releases/nih-scientists-find-treatment-rare-genetic-skin-disorder
2. Baghdassarian H, Blackstone SA, Clay OS, et al. Variant STAT4 and response to ruxolitinib in an autoinflammatory syndrome. N Engl J Med. Published online May 31, 2023. doi:10.1056/nejmoa2202318
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