HKUMed achieves a global breakthrough in personalised stem cell treatment for immunodeficiency patients, emphasising the importance of raising awareness. (From right) Dr Philip Li, immunodeficiency patient Mr Kong and Professor Liu Pengtao.
A collaborative research team, led by Dr Philip Li Hei, Professors Liu Pengtao and Chak-sing Lau from the LKS Faculty of Medicine of the University of Hong Kong (HKUMed), has pioneered a new stem cell model to help personalise treatment for patients suffering from rare forms of immunodeficiency. The research findings were published in the Journal of Allergy and Clinical Immunology [Link to the publication]
Research background and findings
Primary immunodeficiencies, also known as 'inborn errors of immunity', are debilitating diseases, which compromise the immune system, leaving patients highly vulnerable to infections, autoimmunity and even cancer. To date, about 500 primary immunodeficiencies are known, but the list is growing yearly as new diseases emerge. Although individually rare, the overall incidence of primary immunodeficiency is estimated at 1 in 10,000 individuals. Many of these diseases are also caused by genetic mutations and can be inherited across generations.
Owing to their rarity, a significant number of immunodeficiencies remain underdiagnosed and undertreated. Patients with these diseases often lack specific treatment options and receive suboptimal management, leading to a tremendous burden on patients and their families. One example is a rare disorder called STAT1-Gain-of-Function (STAT1-GoF) disease. Patients with STAT1-GoF are born with an inheritable defect in their immune system, making them susceptible to life-threatening infections, autoimmune disorders, aneurysms and cancers.
Collaborating with partners at the Centre for Translational Stem Cell Biology (CTSCB) and the University of Cambridge, HKUMed has pioneered a new stem cell platform to help patients with primary immunodeficiencies. The research team took blood samples from patients and re-engineered the patients' cells into Expanded Potential Stem Cells (EPSCs), which can be used as personalised disease models, enabling various therapies to be tested to identify the most effective and safest treatment options without causing unnecessary risk to the patients. The team has had remarkable success in identifying and repurposing drugs initially used to treat rheumatological conditions to treat individual STAT1-GoF patients in Hong Kong. The team's stem cell platform has demonstrated curative potential of individualised gene therapy for these conditions.
Research significance
'Using our innovative platform, we successfully identified safe, effective and novel treatment options for individuals with rare immunological diseases,' said Dr Philip Li Hei, Division Chief of Rheumatology and Clinical Immunology, and Clinical Assistant Professor, Department of Medicine, School of Clinical Medicine, HKUMed. 'The capability to repurpose existing medications and explore their potential for gene therapy brings tremendous hope to both medical professionals and patients – as many of these "orphan diseases" were once thought to be untreatable or incurable.'
'This study underscores the importance of collaborative research, and the partnership among patients, doctors and scientists,' added Professor Liu Pengtao, Professor of the School of Biomedical Sciences and Managing Director of the Centre for Translational Stem Cell Biology at HKUMed. CTSCB, supported by the InnoHK flagship programme under Innovation and Technology Commission of the HKSAR Government, aims to develop world-leading new stem cell from the state-of-the-art technology. Professor Liu said that this novel stem cell platform has the potential to extend beyond a specific disease or patient, encompassing other inheritable conditions. They have already expanded this platform to study other rare immunological diseases, so hopefully, this is merely the beginning of an extraordinary journey.
Professor Chak-sing Lau, Dean of Medicine and Chair of Rheumatology and Clinical Immunology, Department of Medicine, School of Clinical Medicine, HKUMed emphasised, 'Patients with immunodeficiencies and other rare diseases are often underprivileged in Hong Kong. Delays in diagnoses and inadequate support for expensive diagnostic tests or treatments are common, putting the lives of these patients at risk. With the advent of new treatments, we also urge raising disease awareness, ensuring timely intervention, and providing robust support for immunodeficiency patients in the future.'
About the research team
The research was jointly led by Dr Philip Li Hei, Division Chief of Rheumatology and Clinical Immunology and Clinical Assistant Professor, and Professor Chak-sing Lau, Dean of Medicine and Chair of Rheumatology and Clinical Immunology, from the Department of Medicine, School of Clinical Medicine; and Professor Liu Pengtao, Professor of the School of Biomedical Sciences and Managing Director of the Centre for Translational Stem Cell Biology; at HKUMed. Other researchers were Professor Kenneth Smith and Professor Matthew Cook from University of Cambridge; Dr Liu Xueyan, Dr Vera Chan, Dr Ming Chang, Or Chung-sze, Faria Tsui Tin-wai and Dr Gao Bo from the Centre for Translational Stem Cell Biology.
