Our results indicate that anti-CTLA-4 and anti-PD-1 have distinct predictive biomarker candidates. CD4⁺ and CD8⁺ memory T cell subsets play an important role in response to anti-CTLA-4, and are potential biomarker candidates. For anti-PD-1 therapy, NK cell subsets (but not memory T cell subsets) correlated with clinical response to therapy. These functionally active NK cell subsets likely play a critical role in the anti-tumor response triggered by anti-PD-1.
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Subrahmanyam et al. (2018) studied this question.
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