Autoreactive CD8+ T cells are restrained by an exhaustion-like program that is maintained by LAG3
Year: 2022
Type: article
Source: Nature Immunology
Language: English
Topic: T-cell and B-cell Immunology
Subfield: Immunology
Field: Immunology and Microbiology
Domain: Life Sciences
Open Access status: green
Funders: U.S. Department of Health and Human Services, LEO Fondet, National Institutes of Health, National Human Genome Research Institute, National Cancer Institute, National Institute of Allergy and Infectious Diseases, National Institute of Diabetes and Digestive and Kidney Diseases, Division of Cancer Epidemiology and Genetics, National Cancer Institute
Awards: Testing the role of BATF as a pioneer transcription factor in effector T cells, Special BD LSRFortessaTM, G1644865181, G1796164619, Cellular and transcriptional control of exhausted CD8 T cells lineage dynamics, G2350643484, G2513989095, Investigating a disintegrin and metalloproteinase-mediated Neuropilin 1 cleavage in autoimmune diabetes, G3176075876, Parameters that Underlie Treg Insufficiency in Autoimmune Diabetes, G3892873189, G4553951973, G4834714497, G4848079573, G6558287505, Engineering T cells to Provide Durable Control of HIV-1 Replication, G7381222316, Mechanisms and Immunological Consequences of Host-Virus Interactions, G7742850247, Autoimmunity and Immunopathology Training Program, G8463110223, Linking genome variation to transcriptional network dynamics in human B cells, Durable Alteration of the Human Immune system after Infection or Immunotherapy, Cancer Center Support Grant, Synergies among inhibitory receptors in tolerance and disease, Structure, Function and Mechanistic Analysis of LAG3, Using three-dimensional protein networks to uncover immuno-modulatory molecular phenotypes in infectious disease, Radiation and checkpoint blockade for cancer immune therapy
OpenAlex ID: W4281565387
