Cancer immunotherapy using checkpoint blockade
By Antoni Ribas, J. Wolchok. Science, 2018
5,755 citations recorded by the source corpus.
Subfields: Immunology, Oncology
View Paper: https://www.semanticscholar.org/paper/33d59f45d38e4e9e8e8678f33d679dacc08a1b28
How researchers see this paper
The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.
In Immunology
- Ton N. Schumacher
- J. Wolchok
- Laura M. McLane
- Mohamed S. Abdel-Hakeem
- E. Wherry
- Sandra Hervás-Stubbs
- A. Labani-Motlagh
- K. Polyak
In Oncology
- Ton N. Schumacher
- Laura M. McLane
- Mohamed S. Abdel-Hakeem
- A. Marusyk
- J. Wolchok
- K. Polyak
- E. Wherry
- I. Melero
Citations in the corpus
- Cholesterol induces CD8+ T-cell exhaustion in the tumor microenvironment (2019, positive): “Unprecedented clinical success in a variety of cancers has been achieved by using antibodies to target immune checkpoints on CD8+ T cells, particularly PD-1 antibodies (Callahan et al., 2016; Ribas and Wolchok, 2018).”
- Dysfunctional CD8+ T cells form a proliferative, dynamically regulated compartment within human melanoma (2018, positive): “INTRODUCTION T cell checkpoint blockade therapies that aim to reactivate tumor-specific T cell responses have revolutionized cancer treatment, resulting in durable responses in patients with advanced disease (Ribas and Wolchok, 2018; Sharma and Allison, 2015).”
- Pathophysiology of diabetes: An overview (2020, background): “[118,119] Furthermore, immune checkpoint inhibitors, such as ipilimumab, nivolumab, and pembrolizumab, used in cancer immunotherapy for treatment of advanced-stage cancers, including head and neck cancer, renal cancer, urothelial cancers, non-small-cell lung carcinoma, and melanoma besides other can”
- Targeting DNA damage response promotes anti-tumor immunity through STING-mediated T-cell activation in small cell lung cancer (2019, methodology): “For the PARP inhibitor experiments, mice received one of the following treatments: (1) vehicle; (2) olaparib (50 mg/kg daily) 4 times per week; (3) anti–PD-L1 (300 μg) once per week; or (4) combination of olaparib and anti–PD-L1.”