Reversing thymus involution by targeting long-lived stem cells
Lead Research Organisation:
The Francis Crick Institute
Department Name: Research
Abstract
Ageing is accompanied by increased incidence of disorders that impair quality of life. It is a multifactorial process characterized by a progressive loss of tissue repairing capacity with increased inflammation, infections, and incidence of cancer, degenerative andchronic disorders. There is a need to target a societal major challenge which is represented by the dramatic increased of people aged over 60 years that will double by 2050 with enormous impact on health systems. Due to the intrinsic systemic nature of the immune system interconnecting all organs in our body, progressive immune senescence plays a major role in these age-associated disorders.The thymus is a primary lymphoid organ that provides immunity against pathogens, cancer and establishes long-term immune memory. Nevertheless, the thymus starts involuting with puberty and continue into adulthood with essentially atrophy in the elderly. Aged thymus has reduced capacity to raise response to vaccination and ability to eliminate self-reacting immune cells, contributing to inflammation, autoimmunity and cancer occurrence. Therefore, there is an urgent need to build a novel approach for development of therapeutics able to reverse thymus atrophy. Reversing thymus involution will increase circulating anti-inflammatory immune cells, process known as immune rejuvenation.
The REVERSE THYME project has the main goal to develop a robust screening platform for identification of novel compounds able to activate long-lived, well characterized human epithelial stem cells to restore thymic stroma function and T cell output in aged or damaged thymus. The know-how developed in the host laboratory and our capacity to study thymic epithelial cells from aged and diseased thymi define our competitive advantage to develop a transformative approach to enhance the function of the thymus in several conditions affecting it throughout life and ageing.
The REVERSE THYME project has the main goal to develop a robust screening platform for identification of novel compounds able to activate long-lived, well characterized human epithelial stem cells to restore thymic stroma function and T cell output in aged or damaged thymus. The know-how developed in the host laboratory and our capacity to study thymic epithelial cells from aged and diseased thymi define our competitive advantage to develop a transformative approach to enhance the function of the thymus in several conditions affecting it throughout life and ageing.
Organisations
Publications

Mishto M
(2024)
Proteasome isoforms in human thymi and mouse models.
in Immunology letters
Description | We have established >20 robust primary thymic stem cell cultures from aged individuals suitable for screening and defined their key properties in vitro. We have defined the phenotypic differences from paediatric samples. Furthermore, we have demonstrated robustness, reproducibility, and miniaturisation of our 3D thymic cultures and extended their life to several weeks. These properties are necessary for the high trhough-put screening planned for molecules able to have anti-ageing acivity. |
Exploitation Route | Several private and public sectors interested in health care will have interest in taking the findings to products for anti-ageing. |
Sectors | Healthcare |
Description | Cellular and molecular characterisation of thymic neuroendocrine cells in health and disease |
Amount | £636,858 (GBP) |
Funding ID | MR/Z505808/1 |
Organisation | Medical Research Council (MRC) |
Sector | Public |
Country | United Kingdom |
Start | 08/2024 |
End | 09/2027 |
Description | T-cell replacement therapy for thymic disorders |
Amount | £194,326 (GBP) |
Funding ID | CF-2023-M-2 114 |
Organisation | Rosetrees Trust |
Sector | Charity/Non Profit |
Country | United Kingdom |
Start | 06/2024 |
End | 06/2027 |
Title | THYMIC EPITHELIAL STEM CELLS |
Description | The present invention relates to a newly identified population of thymic epithelial stem cells, methods for their isolation, culture and differentiation, and uses of the cells, in particular their use in therapy, creation of therapeutic thymic constructs and drug screening. |
IP Reference | US2025041346 |
Protection | Patent / Patent application |
Year Protection Granted | 2025 |
Licensed | No |
Title | THYMIC ORGANOIDS |
Description | The present invention provides thymic organoids, methods for their production, hydrogel scaffolds useful in producing thymic organoids, and uses of the thymic organoids, in particular their use in producing human T cells and lymphoid progenitor cells, as well as their use in methods of treating immune disorders and drug screening. |
IP Reference | WO2025045783 |
Protection | Patent / Patent application |
Year Protection Granted | 2025 |
Licensed | No |
Description | MRC workshop on Novel Human In Vitro Models of Complex Disease |
Form Of Engagement Activity | A formal working group, expert panel or dialogue |
Part Of Official Scheme? | No |
Geographic Reach | National |
Primary Audience | Third sector organisations |
Results and Impact | The workshop aimed to identify priority questions, gaps and opportunities to guide further strategic development in this area. The workshop therefore brought together a variety of invited stakeholders with relevant expertise in the field. |
Year(s) Of Engagement Activity | 2024 |