Proliferation of PD-1+ CD8 T cells in peripheral blood after PD-1–targeted therapy in lung cancer patients

Alice O. Kamphorst(Emory University), Rathi N. Pillai(Emory University), Shu Yang(Emory University), Tahseen H. Nasti(Emory University), Rama Akondy(Emory University), Andreas Wieland(Emory University), Gabriel Sica(Emory University), Ke Yu(Emory University), Lydia Koenig(Emory University), Nikita Patel(Emory University), Madhusmita Behera(Emory University), Hong Wu(Emory University), Megan McCausland(Emory University), Zhengjia Chen(Piedmont Cancer Institute), Chao Zhang(Piedmont Cancer Institute), Fadlo R. Khuri(Emory University), Taofeek K. Owonikoko(Emory University), Rafi Ahmed(Emory University), Suresh S. Ramalingam(Emory University)
Proceedings of the National Academy of Sciences
April 26, 2017
Cited by 875Open Access
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Abstract

Significance Therapies that harness the immune system have recently been approved for cancer treatment. Identification of biomarkers to monitor or predict patients’ responses to immunotherapies would help guide treatment decisions. Herein we analyzed changes in peripheral blood T cells from lung cancer patients receiving immunotherapy blocking the PD-1 inhibitory pathway. We detected CD8 T-cell responses following treatment in most patients. In addition, our data suggest that an increase in proliferation of PD-1+ CD8 T cells in the blood within 4 wk of treatment initiation may be associated with positive clinical outcome. Our analysis provides valuable insights into cancer patients’ responses to PD-1–targeted therapies and warrant further studies on peripheral blood biomarkers.


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