Eduki publikatzailea

SI: Structural and functional characterization of the ICOS/ICOSL immune complex

Project Description CORDIS

Specific programme: Marie Sklodowska-Curie Individual Fellowships (IF)
UPV/EHU Partner Status: Coordinator
UPV/EHU PI: Jose Luis Nieva
Project start: 01/09/2018
Project end: 31/08/2021

 

Brief description: T and B lymphocytes are effectors of adaptive immunity. Their dysregulation have dramatic health consequences, and can lead to autoimmunity and blood cancers. Recently, immune receptors involved in dictating the fate of B and T cells have expanded drastically. One of these critical receptor/ligand immune pairs is the inducible costimulatory (ICOS) and its ligand ICOSL, which emerged as a novel T/B-cell co-signalling pathway. The multiple roles reported for this immune complex position ICOS/ICOSL at the centre of attention for immunotherapy. Accordingly, several therapeutic antibodies targeting this immune complex are under clinical investigation. However, structure-function studies of ICOS/ICOSL interaction are critically lacking. This proposal aims to use integrative structural biology to provide molecular details into the function and targeting of the ICOS/ICOSL immune complex. These structural blueprints will contribute to the design of next-generation therapies against autoimmune diseases and cancer. This knowledge, will also serve as the basis to develop agonist antibodies that could act as adjuvants of B cell maturation for vaccine purposes. Therefore, this study will aim to apply fundamental mechanistic approaches to answer biomedical research questions and the outcome will result in advances to both molecular medicine and biology of disease.