FP7Реинтеграция2013–2017

PRR IN IMMUNOTHERAPY · COMBINATIONAL USE OF INNATE IMMUNE RECEPTORS FOR CANCER IMMUNOTHERAPY

7РП — „Хора“ (Действия „Мария Кюри“)

Период
2013-06-01 → 2017-05-31
Финансиране от ЕС
100 000 €
Участници
1
Схема
MC-CIG

Линиите свързват координатора с партньорите.

Накратко на български

Молекули от бактерии се въвеждат в ракови клетки, за да бъдат те разпознавани като патогени и атакувани от имунната система. Това помага за създаването на по-ефективни ваксини и методи за проследяване на имунния отговор при пациенти с рак на кръвта.

Този кратък обзор е генериран от изкуствен интелект

Кратко обяснение, генерирано от езиков модел по текста на CORDIS. Оригиналът е по-долу.

Резултати накратко

COMBINATIONAL USE OF INNATE IMMUNE RECEPTORS FOR CANCER IMMUNOTHERAPY

Fighting cancer is a major public health challenge in Europe. Activating the immune system to fight cancer has been highly challenging, but tremendous progresses on the use of immune activators have been achieved recently. In this context, the modification of cancer cells such that they acquire features normally limited to pathogens may constitutes a promising new approach because it allows patient immune system to target cancer cells like if they were pathogens. Our work has been focused on developing and improving such a treatment. To approach this issue our group relies on different strategy. The first one consists in identifying new molecules normally express by pathogens such as bacteria and introduce those molecules within tumor cells. These modified tumor cells are then used as vaccines to increase antitumor immunity. A second interest in our laboratory is to finely assess the cellular and molecular events engaged upon detection of bacterial products to better design cancer vaccines. Finally, we are trying to translate our findings into clinically relevant strategies to monitor cancer immune responses and treatment for patients suffering blood borne cancers. Here, we identified a previously unknown cellular adaptation of innate immune cells upon the sensing of live bacteria. We found that macrophages adjust the organization and activity of their mitochondrial respiratory chain in response to the detection of live bacteria. In particular, we discovered that the activity of the complex II, an important component of the respiratory chain, is required for optimal response against bacteria. It allows the production of the metabolite fumarate that exhibits antibacterial properties. In addition, complex II activity is required to fine-tune the innate immune response at the level of cytokines production thereby modulating the balance between inflammatory and tolerant immune response. Our findings will benefits the design of new anticancer molecules and strategies that aim at targeting cancer metabolism. It will also help in the design of next generation vaccines that will includes molecules that modulates immune cell metabolism. Our research is thus beneficial for the European community at several levels since it aims at developing new and low cost vaccines and treatments for cancer and infectious diseases. Therefore, many patients should eventually benefit from our research.

Текст от CORDIS, на английски · Данни: CORDIS, © Европейски съюз

Цел на проекта

Cancer is a major scientific and economical challenge that our society has to face and new therapeutic approaches should now be evaluated in order to decrease human and financial cost of this disease. After suffering from many drawbacks, cancer immunotherapy, which aims at mobilizing the immune system to fight cancer, has recently gained enthusiasm with the completion of several randomized phase III clinical trials. Because of their ability to trigger the innate immune responses, ligands for pattern-recognition receptors (PRRs) have been included in several vaccination protocols. These approaches, however, have unveiled new hurdles. Here we propose to investigate a new approach for cancer immunotherapy in Human, based on the use of PRR ligand-containing tumor cells. We have recently shown that introducing the bacterial protein flagellin into tumor cells stimulates innate immune cells and induces a tumor-specific adaptive immunity. Flagellin recognition by myeloid cells engages three distinct PRRs, but subsequent molecular mechanisms controlling presentation of tumor-associated antigens to T lymphocytes are still poorly defined. In addition, the precise nature of adaptive immune responses that efficiently eradicate tumor cells still needs to be precisely characterized before developing pre-clinical trials in Humans. In this context, flagellin-expressing tumor cells represent a powerful tool to uncover fundamental questions on the control of the adaptive immunity by the innate immune system, which will be necessary for the development of new anti-tumor immunotherapies.

Оригинален текст от CORDIS (на английски).

Участници

  • CENTRO NACIONAL DE INVESTIGACIONES CARDIOVASCULARES CARLOS III (F.S.P.) · MadridКоординаторИспания

Връзки

Данни: CORDIS, © Европейски съюз