scispace - formally typeset
J

Jedd D. Wolchok

Researcher at Memorial Sloan Kettering Cancer Center

Publications -  795
Citations -  154490

Jedd D. Wolchok is an academic researcher from Memorial Sloan Kettering Cancer Center. The author has contributed to research in topics: Ipilimumab & Immune system. The author has an hindex of 140, co-authored 713 publications receiving 123336 citations. Previous affiliations of Jedd D. Wolchok include Ludwig Institute for Cancer Research & University of York.

Papers
More filters
Journal ArticleDOI

Targeting AMP kinase in melanoma: A phase I trial of phenformin with dabrafenib/trametinib.

TL;DR: A phase I trial combining phenformin (phen) and dabrafenib/trametinib (dab/Tram) was conducted in patients with metastatic BRAF V600-mutated melanoma (mel) cell lines as mentioned in this paper .
Journal ArticleDOI

Abstract 6150: Potential role of CD47 in T cell exhaustion program

TL;DR: It is confirmed that thrombospondin-1 (TSP-1), as an extracellular matrix protein and a ligand of CD47, contributes to driving the differentiation of CD8 T cells toward exhaustion, and shows that CD47 functions as a negative regulator for T cell proliferation and function during T cell priming.
Posted ContentDOI

Data from Eganelisib, a First-in-Class PI3Kγ Inhibitor, in Patients with Advanced Solid Tumors: Results of the Phase 1/1b MARIO-1 Trial

TL;DR: Eganelisib (IPI-549) is a first-in-class, orally administered, highly selective PI3Kγ inhibitor with antitumor activity alone and in combination with programmed cell death protein 1/ligand 1 (PD-1/PD-L1) inhibitors in preclinical studies as mentioned in this paper .
Journal ArticleDOI

549 Characterizing double positive T cells in the tumor microenvironment: a tale of promiscuous cell fates

TL;DR: The re-expression of the opposite co-receptor following adoptive T cell transfer in B16 melanoma tumor bearing mice is demonstrated and highlighted the capability of single positive T cells to differentiate in response to antigen and local stimuli into novel T cell subsets with polyfunctional characteristics.