RA AND GD T CELLS · The effect of retinoic acid on the fate of γδ T cells
7РП — „Хора“ (Действия „Мария Кюри“)
- Период
- 2014-04-01 → 2016-03-31
- Финансиране от ЕС
- 183 505 €
- Участници
- 1
- Схема
- MC-IEF
Линиите свързват координатора с партньорите.
Накратко на български
Ретиноиновата киселина (активен метаболит на витамин А) и нейният ефект върху γδ Т-клетките се изследват чрез модели на мишки с разсеяна склероза. Това помага да се разбере как се намалява активността на автоимунните клетки, които причиняват възпаления в организма.
Кратко обяснение, генерирано от езиков модел по текста на CORDIS. Оригиналът е по-долу.
Резултати накратко
The effect of retinoic acid on the fate of γδ T cells
Retinoic acid, the active metabolite of vitamin A, can modulate immune responses. In the steady-state, it can help to maintain tolerance against commensal bacteria through the induction of regulatory T cells that suppress immune responses. By contrast, in inflammatory conditions, retinoic acid can promote effector T cells that mediate inflammation. Here we examined the effect of retinoic acid on γδ T cells, a subpopulation of immune cells that play crucial roles in defending the mucosal surfaces of the body against infection but are also involved in sterile inflammation that can lead to autoimmune diseases. Indeed γδ T cells strongly influence many other immune and non-immune cells, especially through their secretion of specialized proteins called cytokines. Thus they can rapidly switch from a pro-inflammatory to an anti-inflammatory state and vice versa, which strongly impacts the behaviour of the other cell types and therefore the equilibrium of the immune system. γδ T cells also have the capacity to be self-reactive, and therefore can play a pathogenic role in the development of autoimmune diseases, such as psoriasis, multiple sclerosis and rheumatoid arthritis. In this study we found that retinoic acid had a dramatic suppressive effect on the pathogenicity of γδ T cells purified from lymph nodes, spleens and skin of mice. Retinoic acid inhibited the capacity of γδ T cells to differentiate, proliferate and respond to pathogenic stimuli. Furthermore, treatment of mice with retinoic acid delayed onset and significantly reduced the symptoms of diseases in a mouse model of a multiple sclerosis. We found that retinoic acid decreased the frequency and activity of the autoreactive γδ T cells and CD4 helper T cells that infiltrate the central nervous system to cause neuroinflammation, a process that leads to nerve damage and gradual paralysis in multiple sclerosis. Furthermore, depletion of γδ T cells reduced the capacity of immune cells to induce the multiple sclerosis-like disease. Interestingly treatment of this single cell type with retinoic acid was enough to prevent immune cells from transferring diseases to recipient mice. Our findings demonstrate that retinoic acid has powerful anti-inflammatory properties in a model of multiple sclerosis that are mediated by suppressing the pathogenic function of γδ T cells. As γδ T cells play a damaging role in a number of autoimmune diseases, our findings have implications for the treatment of these diseases, but also suggest that simple dietary interventions that involve consumption of vegetable rich in vitamin A may help to re-set the immune imbalance in these debilitating diseases.
Текст от CORDIS, на английски · Данни: CORDIS, © Европейски съюз
Цел на проекта
Retinoic acid, the active metabolite of vitamin A, is implicated in a broad range of well-studied pre- and post-natal functions. By comparison, its involvement in the development and function of the immune system remains largely unknown. However, it has recently been shown that retinoic acid has a protective effect in a murine model of colitis by switching the cytokine production by γδ T cells from pro- (IL-17A) to anti-inflammatory (IL-22). At the border between innate and adaptive immunity, γδ T cells constitute an important part of the immune system and are highly involved in the pathogenesis of several autoimmune or infectious disorders. Although these cells are found throughout the immune system, they can be divided into subpopulations which are interestingly enhanced in the compartments located at environmental interfaces such as the skin, intestine, uterus and lungs. Throughout this fellowship, I propose to (1) study the molecular mechanisms by which retinoic acid is able to change the fate of γδ T cells, (2) analyze the differential impact of retinoic acid between the γδ T cell subtypes, and (3) study the influence of retinoic acid in vivo, in two different autoimmune disorders, psoriasis and experimental autoimmune encephalomyelitis. This study will highlight γδ T cells as new therapeutic targets and retinoids as immunomodulators for the development of efficient immunotherapies, a highly promising challenge in medical research for the future treatment of cancers, autoimmune and infectious disorders.
Оригинален текст от CORDIS (на английски).
Участници
- THE PROVOST, FELLOWS, FOUNDATION SCHOLARS & THE OTHER MEMBERS OF BOARD, OF THE COLLEGE OF THE HOLY & UNDIVIDED TRINITY OF QUEEN ELIZABETH NEAR DUBLIN · DublinКоординаторИрландия
Връзки
Данни: CORDIS, © Европейски съюз
