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Agonist immunotherapy restores T cell function following MEK inhibition improving efficacy in breast cancer.

Nat Commun. 2017; 
Dushyanthen Sathana,Teo Zhi Ling,Caramia Franco,Savas Peter,Mintoff Christopher P,Virassamy Balaji,Henderson Melissa A,Luen Stephen J,Mansour Mariam,Kershaw Michael H,Trapani Joseph A,Neeson Paul J,Salgado Roberto,McArthur Grant A,Balko Justin M,Beavis Paul A,Darcy Phillip K,Loi She
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Peptide Synthesis (OT-II) peptide (GenScript; 300 nM) for 3–4 days and supplemented with daily IL-2 (100 units/ml Get A Quote

摘要

The presence of tumor-infiltrating lymphocytes in triple-negative breast cancers is correlated with improved outcomes. Ras/MAPK pathway activation is associated with significantly lower levels of tumor-infiltrating lymphocytes in triple-negative breast cancers and while MEK inhibition can promote recruitment of tumor-infiltrating lymphocytes to the tumor, here we show that MEK inhibition adversely affects early onset T-cell effector function. We show that α-4-1BB and α-OX-40 T-cell agonist antibodies can rescue the adverse effects of MEK inhibition on T cells in both mouse and human T cells, which results in augmented anti-tumor effects in vivo. This effect is dependent upon increased downstream p38/JNK p... More

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