Targeting of cancer neoantigens with donor-derived T cell receptor repertoires

Author:

Strønen Erlend12,Toebes Mireille3,Kelderman Sander3,van Buuren Marit M.3,Yang Weiwen12,van Rooij Nienke3,Donia Marco4,Böschen Maxi-Lu12,Lund-Johansen Fridtjof25,Olweus Johanna12,Schumacher Ton N.3

Affiliation:

1. Department of Cancer Immunology, Oslo University Hospital Radiumhospitalet, Oslo, Norway.

2. K. G. Jebsen Centers for Cancer Immunotherapy and for Inflammation Research, Institute for Clinical Medicine, University of Oslo, Oslo, Norway.

3. Division of Immunology, Netherlands Cancer Institute, Amsterdam, Netherlands.

4. Center for Cancer Immune Therapy, Department of Hematology, Herlev Hospital, University of Copenhagen, Herlev, Denmark.

5. Department of Immunology and Transfusion Medicine, Oslo University Hospital Rikshospitalet, Oslo, Norway.

Abstract

Outsourcing cancer immunotherapy Successful cancer immunotherapy depends on a patient's T cells recognizing tumor-specific mutations and then waging a lethal attack. Despite tumors harboring many mutations, most individuals have very few T cells that respond to these so-called “neo-antigens.” Strønen et al. isolated T cells from healthy donors that responded to predicted neo-antigens expressed by melanomas taken from three patients, sometimes including neo-antigens that the patient's own T cells ignored (see the Perspective by Yadav and Delamarre). Testing whether such an outsourcing strategy could improve clinical outcomes will be an important next step. Science , this issue p. 1337 ; see also p. 1275

Funder

Dutch Cancer Society Queen Wilhelmina

K. G. Jebsen Foundation

Research Council of Norway

Regional Authorities South-Eastern Norway

University of Oslo

Oslo University Hospital

Norwegian Cancer Society

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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