The nuclear export protein XPO1 provides a peptide ligand for natural killer cells

Author:

Blunt Matthew D.1ORCID,Fisher Hayden234ORCID,Schittenhelm Ralf B.5ORCID,Mbiribindi Berenice1,Fulton Rebecca1ORCID,Khan Sajida1ORCID,Espana-Serrano Laura1ORCID,Graham Lara V.1ORCID,Bastidas-Legarda LeidyORCID,Burns Daniel1,Khakoo Sophie M.S.1,Mansour Salah1ORCID,Essex Jonathan W.3ORCID,Ayala Rochelle6ORCID,Das Jayajit7ORCID,Purcell Anthony W.6ORCID,Khakoo Salim I.1ORCID

Affiliation:

1. School of Clinical and Experimental Sciences, Faculty of Medicine, University of Southampton, Southampton, UK.

2. School of Cancer Sciences, Faculty of Medicine, University of Southampton, Southampton, UK.

3. School of Chemistry, Faculty of Engineering and Physical Sciences, University of Southampton, Southampton, UK.

4. School of Biological Sciences, Faculty of Environmental and Life Sciences, University of Southampton, Southampton, UK.

5. Monash Proteomics & Metabolomics Platform, Biomedicine Discovery Institute and Department of Biochemistry and Molecular Biology, Monash University, Clayton, Victoria, Australia.

6. Biomedicine Discovery Institute and Department of Biochemistry and Molecular Biology, Monash University, Clayton, Victoria, Australia.

7. Steve and Cindy Rasmussen Institute for Genomic Medicine, Abigail Wexner Research Institute, and The Department of Pediatrics, Pelotonia Institute for Immuno-Oncology, Ohio State University, Columbus, OH, USA.

Abstract

XPO1 (Exportin-1/CRM1) is a nuclear export protein that is frequently overexpressed in cancer and functions as a driver of oncogenesis. Currently small molecules that target XPO1 are being used in the clinic as anticancer agents. We identify XPO1 as a target for natural killer (NK) cells. Using immunopeptidomics, we have identified a peptide derived from XPO1 that can be recognized by the activating NK cell receptor KIR2DS2 in the context of human leukocyte antigen–C. The peptide can be endogenously processed and presented to activate NK cells specifically through this receptor. Although high XPO1 expression in cancer is commonly associated with a poor prognosis, we show that the outcome of specific cancers, such as hepatocellular carcinoma, can be substantially improved if there is concomitant evidence of NK cell infiltration. We thus identify XPO1 as a bona fide tumor antigen recognized by NK cells that offers an opportunity for a personalized approach to NK cell therapy for solid tumors.

Publisher

American Association for the Advancement of Science (AAAS)

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