iPSC-derived NK cells maintain high cytotoxicity and enhance in vivo tumor control in concert with T cells and anti–PD-1 therapy

Author:

Cichocki Frank1ORCID,Bjordahl Ryan2,Gaidarova Svetlana2,Mahmood Sajid2,Abujarour Ramzey2,Wang Hongbo1ORCID,Tuininga Katie1,Felices Martin1,Davis Zachary B.1,Bendzick Laura1,Clarke Raedun2ORCID,Stokely Laurel2ORCID,Rogers Paul2,Ge Moyar2,Robinson Megan2ORCID,Rezner Betsy2,Robbins David L.2ORCID,Lee Tom T.2ORCID,Kaufman Dan S.3ORCID,Blazar Bruce R.4ORCID,Valamehr Bahram2ORCID,Miller Jeffrey S.1ORCID

Affiliation:

1. Department of Medicine, University of Minnesota, Minneapolis, MN 55455, USA.

2. Fate Therapeutics, San Diego, CA 92121, USA.

3. Department of Medicine, Division of Regenerative Medicine, Moores Cancer Center, and Sanford Consortium for Regenerative Medicine, University of California, San Diego, La Jolla, CA 92093, USA.

4. Department of Pediatrics, University of Minnesota, Minneapolis, MN 55455, USA.

Abstract

Natural killer cells derived from iPSCs prime T cells for anti–PD-1 immune checkpoint therapy.

Funder

National Heart, Lung, and Blood Institute

National Cancer Institute

Publisher

American Association for the Advancement of Science (AAAS)

Subject

General Medicine

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