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Tiziana Life Sciences Announces Groundbreaking Study Published in Nature Neuroscience Demonstrating Positive Results for Nasal Anti-CD3 Therapy in Traumatic Brain Injury

In This Article:

Tiziana Life Sciences Ltd.
Tiziana Life Sciences Ltd.
  • Traumatic brain injury is a leading cause of death and disability

  • Currently, there is no treatment to prevent the long-term effects of traumatic brain injury

  • Findings could translate into treating intracerebral hemorrhage or stroke

NEW YORK, Feb. 27, 2025 (GLOBE NEWSWIRE) -- Tiziana Life Sciences, Ltd. (Nasdaq: TLSA) (“Tiziana” or the “Company”), a biotechnology company developing breakthrough immunomodulation therapies with its lead development candidate, intranasal foralumab, a fully human, anti-CD3 monoclonal antibody, today announced the publication of a landmark study in Nature Neuroscience demonstrating that nasal administration of Tiziana’s anti-CD3 monoclonal antibody significantly reduced neuroinflammation and improved recovery. Modulating the neuroinflammatory response correlated with improved neurological outcomes. These included, less anxiety, less cognitive decline, and improved motor skills, in a preclinical model of traumatic brain injury (TBI).

The study was led by Saef Izzy, MD, FNCS, FAAN, a neurologist and head of the Immunology of Brain Injury Program at Brigham and Women’s Hospital (BWH), a founding member of the Mass General Brigham healthcare system. The publication revealed that nasal anti-CD3 therapy induces IL-10 producing regulatory T cells (Tregs) that migrate to the brain and modulate microglia activity. These Tregs were found to play a pivotal role in reducing chronic microglial inflammation and enhancing their phagocytic function, ultimately mitigating CNS damage and behavioral deficits associated with TBI.

“This study highlights the critical role of immune modulation in improving recovery time and outcomes after traumatic brain injury,” said Dr. Saef Izzy, lead author and neurologist at Brigham and Women’s Hospital. “We found that nasal anti-CD3 therapy effectively harnesses the body’s own immune system to counteract the damaging effects of neuroinflammation while enhancing the brain’s reparative mechanisms. These findings offer exciting potential for developing a much-needed therapeutic approach for TBI patients.”

TBI remains a major unmet medical need, with no effective treatments currently available to reduce CNS injury and promote recovery. The study demonstrated that blocking the IL-10 receptor abrogated the benefits of nasal anti-CD3, confirming the pivotal role of IL-10 in the therapeutic effect. Moreover, the adoptive transfer of IL-10 producing Tregs restored the benefits, further validating the mechanism of action.

“The positive results from this study provide strong support for advancing nasal anti-CD3 (foralumab) as a novel and promising treatment for traumatic brain injury,” said Dr. Howard L. Weiner, Co-Director of the Ann Romney Center for Neurologic Diseases at BWH. “By modulating the immune system through simple nasal delivery, we are tapping into a unique and innovative way to treat neuroinflammation and improve outcomes for TBI patients, which could be in a hospital, at the road side after an accident or on the playing field in contact sports.”