Clinical blockade of PD1 and LAG3 — potential mechanisms of action
By L. Nguyen, P. Ohashi. Nature reviews. Immunology, 2014
602 citations recorded by the source corpus.
Subfields: Immunology, Oncology
View Paper: https://www.semanticscholar.org/paper/73e49cd55a5077fa5c48ae928426cea22c571b18
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In Immunology
Citations in the corpus
- Autophagy, ferroptosis, pyroptosis, and necroptosis in tumor immunotherapy (2022, background): “Traditionally, it was believed that immunotherapyactivated CD8+ T cells induce tumor cell death mainly through the perforin-granzyme pathway and the Fas-Fas ligand (FASL) pathway.(26,27) However, many studies have surprisingly revealed that CD8+ T cells can suppress tumors by inducing ferroptosis an”
- Single-cell RNA-seq enables comprehensive tumour and immune cell profiling in primary breast cancer (2017, unknown): “47) have begun.”
- Next generation of immune checkpoint therapy in cancer: new developments and challenges (2018, background): “Targeting LAG-3 with antagonistic mAbs interferes with the LAG-3 interaction between MCH II molecules expressed by tumor and/or immune cells, promoting tumor cell apoptosis [19].”