PD-1 and its ligands in tolerance and immunity.
By M. Keir, M. Butte, G. Freeman, Arlene H. Sharpe. Annual Review of Immunology, 2008
5,308 citations recorded by the source corpus.
Subfields: Immunology, Oncology
View Paper: https://www.semanticscholar.org/paper/81cd0d4f30bf150b3f46b0aa32a761c3e11e2812
How researchers see this paper
The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.
In Immunology
- E. Wherry
- D. Pardoll
- G. Freeman
- Arlene H. Sharpe
- A. Schietinger
- P. Greenberg
- Rafi Ahmed
- Kristen E. Pauken
In Oncology
- D. Pardoll
- E. Wherry
- James P. Allison
- G. Freeman
- Kristen E. Pauken
- Arlene H. Sharpe
- M. Smyth
- A. Schietinger
Citations in the corpus
- Challenges in liver cancer and possible treatment approaches (2019, background): “Designing mAbs against the immune checkpoint regulator, PD-1, reduces T-cell apoptosis, potentiates antitumor immunity, and inhibits cell proliferation [74, 75].”
- Overcoming T cell exhaustion in infection and cancer (2015, background): “Studies in preclinical models have greatly contributed to our understanding of the PD-1 pathway in the regulation of T cell immunity [3, 37, 96].”
- T cell costimulatory receptor CD28 is a primary target for PD-1–mediated inhibition (2016, background): “In addition, T cell activation increases the expression of PD-1 on the T cell itself (3).”
- The Pathogenesis of Sepsis (2011, background): “PD-L2 is more restricted and is inducible only on dendritic cells, macrophages, bone marrow–derived mast cells, and specific peritoneal B cells (31, 32).”