HEИндивидуална стипендия2026–2028

ReTenTion · Next Generation Immune Checkpoint Inhibitor for Cancer Therapy

„Хоризонт Европа“ — Действия „Мария Склодовска-Кюри“

Период
2026-02-15 → 2028-02-14
Финансиране от ЕС
216 240 €
Участници
2
Схема
HORIZON-TMA-MSCA-PF-EF

Линиите свързват координатора с партньорите.

Накратко на български

Нови антитела с по-малък размер се тестват за по-добро проникване в туморите и блокиране на клетките, които потискат имунния отговор. Това може да подобри ефективността на терапията при пациенти, които не реагират на стандартните методи за лечение.

Този кратък обзор е генериран от изкуствен интелект

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

Цел на проекта

Immune checkpoint inhibitors (ICIs) for cancer therapy have revolutionized the treatment of several cancers. These ICIs are made from monoclonal antibodies that antagonize inhibitory signals via cytotoxic T-lymphocyte- associated antigen-4 (CTLA-4) and programmed cell death protein-1 (PD-1) that block the tumoricidal activity of T cells. Although these ICIs have improved the overall survival of cancer patients such as cutaneous melanoma patients, only one third of patients has remained progression-free 5 years after initiating ICI therapy. This low efficacy is largely due to (1) the presence of immune suppressive regulatory T cells (Treg) within tumor microenvironment (TME) (2) the lack of efficacy of tumor penetration and retention. To improve the current ICI, this project RenTenTion aims to develop a next generation ICIs with smaller molecule so called single domain antibody (sdAb), give rise to enhanced tumor penetration. Targeting against a new immune checkpoint molecule 41-BB that highly expressed by intratumoral Treg, this next generation sdAb based ICI will inhibit tumor promoting immune cells Treg, while stimulate tumor rejecting immune cells such as effector T cells in tumors. Additionally, this project will couple the sdAb with collagen binding domain receptor so called leukocyte-associated immunoglobulin-like receptor 1 (LAIR1) that bind to collagen in the tumor, therefore sustain tumor retention. This project “ReTenTion” will fill a gap for a strong need for new ICI molecules capable of addressing immunosuppressive in TME, yet smaller than conventional ICIs, boosting passive delivery.

Оригинален текст от CORDIS (на английски).

Участници

  • VRIJE UNIVERSITEIT BRUSSEL · Bruxelles / BrusselКоординаторБелгия
  • ETHERNA IMMUNOTHERAPIES · NielБелгия

Връзки

Данни: CORDIS, © Европейски съюз