CTLA-4 and PD-1/PD-L1 Blockade: New Immunotherapeutic Modalities with Durable Clinical Benefit in Melanoma Patients
By P. Ott, F. Hodi, C. Robert. Clinical Cancer Research, 2013
646 citations recorded by the source corpus.
Subfields: Molecular Biology, Oncology
View Paper: https://www.semanticscholar.org/paper/45de0572cb632d4785cb15b0b0ba39c073d2dba7
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Citations in the corpus
- PD-1 and PD-L1 Checkpoint Signaling Inhibition for Cancer Immunotherapy: Mechanism, Combinations, and Clinical Outcome (2017, background): “Efforts to use monoclonal antibodies (mAbs) to target and block these immunoinhibitory interactions have led to a new era of immunotherapy based agents for cancer therapy (Freeman et al., 2000; Topalian et al., 2012; Ott et al., 2013).”
- OMIP‐050: A 28‐color/30‐parameter Fluorescence Flow Cytometry Panel to Enumerate and Characterize Cells Expressing a Wide Array of Immune Checkpoint Molecules (2018, background): “Immunotherapy has shown clinical benefit in certain solid tumors, although the markers predicting a successful response remain poorly defined (1).”
- CTLA-4 and PD-1 Pathways (2016, background): “This has the potential to provide a more targeted signal with less unwanted toxicity, as selftolerance mediated through PD-1:PD-L2 interactions should be preserved.(37,49) Furthermore, as PD-L1 is known to bind CD80 as well as PD-1 to deliver inhibitory signals to T cells,(33) PDL1 inhibition with a”