Clinical landscape of LAG-3-targeted therapy

Lymphocyte-activated gene 3 (LAG-3) is a cell surface inhibitory receptor and a key regulator of immune homeostasis with multiple biological activities related to T-cell functions. LAG-3 is considered a next-generation immune checkpoint of clinical importance, right next to programmed cell death pro...

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Detalles Bibliográficos
Autores: Chocarro, L. (Luisa)|||/items/6f7649fe-4d5c-4596-8bff-0a4c4797e891, Blanco, E. (E.)|||/items/3c3d9a55-d64a-4217-886d-6a04985434e8, Arasanz, H. (Hugo)|||/items/af58f0cb-4fe5-409c-a96a-b2a6b6831b48, Fernández-Rubio, L. (Leticia)|||/items/5a8093ff-35ec-4a3f-9eee-80fa67527bcb, Bocanegra, A. (Ana)|||/items/bb0c2c14-2f4e-4fcb-a6de-a1268735f4cd, Echaide, M. (Miriam)|||/items/0595e71d-30a1-44e1-ae67-68a8da14f897, Garnica-Ochoa, M. (Maria)|||/items/49a72ee4-dddc-4114-be65-7830aeb1b5c3, Ramos, P. (Pilar)|||/items/8117329a-a1ba-4aa5-a8b8-5e963f214ac5, Fernández-Hinojal, G. (Gonzalo)|||/items/6a8e64fe-0006-4d63-885f-3c030209f545, Vera, R. (Ruth)|||/items/c5e822da-e29b-4f65-bb1c-be8bb5b999e1, Kochan, G. (Grazyna)|||/items/bf76a215-0675-467b-bb79-f2b4192fa4b2, Escors, D. (David)|||/items/82737dd6-3010-4c11-ae0f-a6efb4f177a6
Tipo de recurso: artículo
Fecha de publicación:2022
País:España
Institución:Universidad de Navarra
Repositorio:Dadun. Depósito Académico Digital de la Universidad de Navarra
Idioma:inglés
OAI Identifier:oai:dadun.unav.edu:10171/123228
Acceso en línea:https://hdl.handle.net/10171/123228
Access Level:acceso abierto
Palabra clave:LAG-3
Cancer Treatment
Immune Checkpoint
Immunotherapy
Targeted Therapy
Descripción
Sumario:Lymphocyte-activated gene 3 (LAG-3) is a cell surface inhibitory receptor and a key regulator of immune homeostasis with multiple biological activities related to T-cell functions. LAG-3 is considered a next-generation immune checkpoint of clinical importance, right next to programmed cell death protein 1 (PD-1) and cytotoxic T-cell lymphocyte antigen-4 (CTLA-4). Indeed, it is the third inhibitory receptor to be exploited in human anticancer immunotherapies. Several LAG-3-antagonistic immunotherapies are being evaluated at various stages of preclinical and clinical development. In addition, combination therapies blocking LAG-3 together with other immune checkpoints are also being evaluated at preclinical and clinical levels. Indeed, the co-blockade of LAG-3 with PD-1 is demonstrating encouraging results. A new generation of bispecific PD-1/LAG-3-blocking agents have also shown strong capacities to specifically target PD-1+ LAG-3+ highly dysfunctional T cells and enhance their proliferation and effector activities. Here we identify and classify preclinical and clinical trials conducted involving LAG-3 as a target through an extensive bibliographic research. The current understanding of LAG-3 clinical applications is summarized, and most of the publically available data up to date regarding LAG-3-targeted therapy preclinical and clinical research and development are reviewed and discussed.