Inhibiting the protein PD-1 can activate T cells that trigger immune responses against tumour cells. But it emerges that, in mice, this immunotherapy exacerbates a cancer that involves the T cells themselves. See Letter p.121
Notes
References
Wartewig, T. et al. Nature 552, 121–125 (2017).
Sharpe, A. H. & Pauken, K. E. Nature Rev. Immunol. http://doi.org/gb2z5d (2017).
Navarro, M. N. & Cantrell, D. A. Nature Immunol. 15, 808–814 (2014).
Wolchok, J. D. et al. N. Engl. J. Med. 377, 1345–1356 (2017).
Borghaei, H. et al. N. Engl. J. Med. 373, 1627–1639 (2017).
Hude, I., Sasse, S., Engert, A. & Bröckelmann, P. J. Haematologica 102, 30–42 (2017).
Wei, S. C. et al. Cell 170, 1120–1133 (2017).
Gordon, S. R. et al. Nature 545, 495–499 (2017).
Lesokhin, A. M. et al. J. Clin. Oncol. 34, 2698–2704 (2016).
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Ludin, A., Zon, L. The dark side of PD-1 receptor inhibition. Nature 552, 41–42 (2017). https://doi.org/10.1038/nature24759
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DOI: https://doi.org/10.1038/nature24759
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