Molecular Pathways: Next-Generation Immunotherapy—Inhibiting Programmed Death-Ligand 1 and Programmed Death-1
By Daniel S. Chen, Bryan A. Irving, Stephen F. Hodi. Clinical Cancer Research, 2012
612 citations recorded by the source corpus.
Subfields: Immunology, Oncology
View Paper: https://www.semanticscholar.org/paper/fd8df0f2d4509b39f079c5279180c0781f5d19fc
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In Immunology
In Oncology
Citations in the corpus
- Immune Checkpoint Inhibitors in Cancer Therapy (2022, background): “The expression of PD-L1 was also found to impair cytotoxic T lymphocyte (CTL) protection and reduce chronic viral infections [100].”
- The Where, the When, and the How of Immune Monitoring for Cancer Immunotherapies in the Era of Checkpoint Inhibition (2016, background): “PD-L1 is strongly induced by IFNg , resulting in adaptive expression on tumor cells and tumor-infiltrating immune cells as a negative feedback mechanism (23, 24).”
- Oncology meets immunology: the cancer-immunity cycle. (2013, background): “This class of molecules, including PD-L1:PD-1 (reviewed in Chen et al., 2012; Topalian et al., 2012a), emphasizes that the immune response in cancer reflects a series of carefully regulated events that may be optimally addressed not singly but as a group.”
- Classifying cancers based on T cell infiltration and PD-L1 (2015, positive): “219 This suggests that the degree of mutagenesis may directly or 220 indirectly correlate with the degree of immunogenicity of any 221 given tumor (37).”
- Predictive correlates of response to the anti-PD-L1 antibody MPDL3280A in cancer patients (2014, background): “1) by physical examination and radiographic assessment, primarily computed tomography scan30 and immune-related response criteria17; and/or (2) loss of clinical benefit as assessed by the investigator; and/or (3) unacceptable toxicity as assessed by the investigator.”