Stem Cell Shots Unveil a Safer Way To Treat Inflammatory Eye Diseases
Inflammatory eye diseases can be challenging to treat, with medications like corticosteroids causing unwanted complications.
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Inflammatory eye diseases can be challenging to treat, with medications like corticosteroids causing unwanted complications such as glaucoma. However, a study led by researchers from Fujita Health University, Japan, offers hope. The team discovered that local injections of mesenchymal stem cells into periocular tissue can significantly reduce inflammation in conditions such as chronic graft-versus-host disease. These findings offer hope for a safer, more targeted alternative to conventional treatments for ocular inflammatory diseases.
Graft-versus-host disease (GVHD) is a common and severe complication that occurs after stem cell transplantation, where the donor’s immune cells attack the recipient’s tissues. Ocular manifestation of GVHD is among the most challenging to treat, often leading to chronic inflammation and corneal tissue damage, which can result in loss of vision. Conventional treatments, including corticosteroids, are frequently used to manage ocular inflammation associated with GVHD. However, these therapies come with significant side effects, including the risk of glaucoma and other ocular complications.
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Subscribe for FREENow, in a new study conducted by Dr. Shigeto Shimmura and Robert M. Rusch from Fujita Health University and Keio University, Japan, researchers have proposed a novel therapy for ocular GVHD involving MSCs. The team explored the potential of regenerative mesenchymal stem cells in reducing ocular inflammation in GVHD-infected mice. Their study, published in The Ocular Surface, explores the potential of adipose-derived MSCs (adMSCs) to reduce inflammation and promote tissue repair. It was made available online on November 13, 2024, and published in Volume 34 of the journal in October 2024.
Elaborating on the rationale behind this study, Dr. Shimmura says, “adMSCs are easy to obtain and have demonstrated benefits in corneal tissue regeneration. Moreover, we injected adMSCs after the onset of GVHD and also monitored them over an extended period of time, helping us verify their therapeutic applicability.”
Using mice that had been induced with chronic GVHD, researchers administered adMSCs into the eyes via a single injection. Over three weeks, the researchers found that the adMSC treatment increased regulatory T cells while reducing inflammation in the mice. Further, adMSC-conditioned media enhanced cell migration and proliferation in laboratory scratch tests, showcasing the regenerative capacity of the cells. Importantly, the injected cells disappeared within a week, minimizing the risk of long-term complications such as tumor formation.
“Our findings highlight the dual benefits of adMSCs: They suppress inflammation and enhance tissue healing,” elaborates Dr. Shimmura, senior author and researcher. Adding further, he says, “This makes them a promising candidate for treating immune-related ocular disorders without systemic side effects.”
These observations point to the potential of adMSCs as a targeted, localized therapy for immune-related eye conditions. Unlike systemic treatments, these local injections ensured the therapeutic effects remained localized to the ocular surface. “Our work underscores the safety and efficacy of adMSCs, paving the way for clinical trials in humans,” notes Dr. Shimmura.
With their immunoregulatory and regenerative properties, adMSCs may offer a lifeline to patients suffering from chronic ocular GVHD and related inflammatory diseases. Future studies, however, need to focus on dose optimization and delivery methods to maximize therapeutic outcomes.
In summary, these results offer hope for a future where innovative, stem cell-based therapies can transform the way we manage autoimmune diseases, offering patients better outcomes and improved quality of life.
Reference: Rusch RM, Inagaki E, Taniguchi H, et al. Adipose-derived mesenchymal stromal cells: A study on safety and efficacy in ocular inflammation. Ocul. Surf. 2024. doi: 10.1016/j.jtos.2024.11.001
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