Researchers have revealed that boosting the key protein Irak-M in eye cells could prevent age related vision loss. This protein plays a vital role for protecting the layer of cells essential for maintaining a healthy retina.
Front cover from June’s Science Translational Medicine showing rescued retinal pigment epithelium (RPE) cells following Irak-M gene therapy.
(Source: Liu et al./Science Translational Medicine)
Bristol/UK – Progression of age-related macular degeneration (AMD) — a common condition impacting central vision, for which there are currently no effective treatments, affects around 200-million people worldwide. This number is expected to rise to 288-million by 2040 as the population ages. This new breakthrough could lead to new and more effective AMD treatments.
AMD can severely impact a person’s vision. Patients suffering from AMD often start with blurred vision or seeing a black dot in their central vision, which can ultimately expand to the point where there is no useful central vision. The exact cause of AMD is complex and thought to involve a combination of aging, genetics, environment and lifestyle factors.
Primarily affecting people over the age of 50, the risk of developing AMD significantly increases with age and makes tasks like reading and driving difficult.
Scientists believe that chronic inflammation, which is typical with aging, is associated with the reduction of a key immune regulatory protein called Irak-M. This protein is crucial for protecting the retinal pigment epithelium (RPE), a layer of cells essential for maintaining a healthy retina. When RPE cells are damaged, it can result in serious eye conditions and vision loss.
In this study, researchers investigated the role of Irak-M in AMD by examining genetic variations and their link to AMD risk. By studying Irak-M levels in patient samples and mouse models of retinal degeneration, the team observed changes in retinal function in mice lacking the Irak3 gene, which expresses the Irak-M protein. They found that Irak-M decreases with age, especially in the retinal pigment epithelium (RPE), and this decline is more pronounced in those with age-related macular degeneration (AMD).
The team then sought to explore whether increasing Irak-M could protect retinal cells from degeneration in mouse models and whether it is a potential therapeutic target for macular degeneration. They show that increasing Irak-M levels through RPE-specific gene delivery helps protect against the effects of aging and oxidative stress and reduces retinal degeneration.
Andrew Dick, Professor of Ophthalmology from Bristol Medical School at the University of Bristol, Director of the UCL Institute of Ophthalmology and one of the study’s lead authors, says: “Our findings suggest that boosting a protein called Irak-M could be a potential treatment strategy for AMD and could offer an exciting new therapeutic target for this common condition for which effective therapies remain elusive.”
Dr. Jian Liu, the lead author and senior research scientist at the Academic Unit of Ophthalmology at the University of Bristol, adds: “Since age stands as the primary risk factor for AMD, the gradual decrease of Irak-M levels with age and a further decline in AMD signifies intricate biological mechanisms underlying the disease’s development and suggests a potential marker of early AMD progression.”
The authors aim to help develop the therapies further through a new University of Bristol spin-out company called Cirrus Therapeutics.
Dr. Ying Kai Chan, Cirrus Therapeutics co-founder and Chief Executive Officer, and one of the study’s co-lead authors, says: “This discovery will build and improve upon current treatments for AMD, which are targeting single pathophysiology pathways. Our novel approach not only addresses the multiple pathways involved in treating AMD but also offers the most compelling and evidence-based strategy available today.”
The research was funded by the Rosetrees Trust; Stoneygate Trust; Underwood Trust; Macular Society; Sight Research UK; Moran Eye Center and Sharon Eccles Steele Center for Translational Medicine (SCTM) at the University of Utah, USA, and supported by the National Institute for Health and Care Research (NIHR) BRC Moorfields and UCL-Institute of Ophthalmology.
Date: 08.12.2025
Naturally, we always handle your personal data responsibly. Any personal data we receive from you is processed in accordance with applicable data protection legislation. For detailed information please see our privacy policy.
Consent to the use of data for promotional purposes
I hereby consent to Vogel Communications Group GmbH & Co. KG, Max-Planck-Str. 7-9, 97082 Würzburg including any affiliated companies according to §§ 15 et seq. AktG (hereafter: Vogel Communications Group) using my e-mail address to send editorial newsletters. A list of all affiliated companies can be found here
Newsletter content may include all products and services of any companies mentioned above, including for example specialist journals and books, events and fairs as well as event-related products and services, print and digital media offers and services such as additional (editorial) newsletters, raffles, lead campaigns, market research both online and offline, specialist webportals and e-learning offers. In case my personal telephone number has also been collected, it may be used for offers of aforementioned products, for services of the companies mentioned above, and market research purposes.
Additionally, my consent also includes the processing of my email address and telephone number for data matching for marketing purposes with select advertising partners such as LinkedIn, Google, and Meta. For this, Vogel Communications Group may transmit said data in hashed form to the advertising partners who then use said data to determine whether I am also a member of the mentioned advertising partner portals. Vogel Communications Group uses this feature for the purposes of re-targeting (up-selling, cross-selling, and customer loyalty), generating so-called look-alike audiences for acquisition of new customers, and as basis for exclusion for on-going advertising campaigns. Further information can be found in section “data matching for marketing purposes”.
In case I access protected data on Internet portals of Vogel Communications Group including any affiliated companies according to §§ 15 et seq. AktG, I need to provide further data in order to register for the access to such content. In return for this free access to editorial content, my data may be used in accordance with this consent for the purposes stated here. This does not apply to data matching for marketing purposes.
Right of revocation
I understand that I can revoke my consent at will. My revocation does not change the lawfulness of data processing that was conducted based on my consent leading up to my revocation. One option to declare my revocation is to use the contact form found at https://contact.vogel.de. In case I no longer wish to receive certain newsletters, I have subscribed to, I can also click on the unsubscribe link included at the end of a newsletter. Further information regarding my right of revocation and the implementation of it as well as the consequences of my revocation can be found in the data protection declaration, section editorial newsletter.
Paper: ‘Replenishing Irak-M expression in retinal pigment epithelium attenuates outer retinal degeneration’ by Jian Liu et al. in Science Translational Medicine