Landscape of immunogenic tumor antigens in successful immunotherapy of virally induced epithelial cancer

Author:

Stevanović Sanja1ORCID,Pasetto Anna2,Helman Sarah R.1ORCID,Gartner Jared J.2,Prickett Todd D.2,Howie Bryan3,Robins Harlan S.34ORCID,Robbins Paul F.2,Klebanoff Christopher A.56,Rosenberg Steven A.2,Hinrichs Christian S.1ORCID

Affiliation:

1. Experimental Transplantation and Immunology Branch, National Cancer Institute, Bethesda, MD 20892, USA.

2. Surgery Branch, National Cancer Institute, Bethesda, MD 20892, USA.

3. Adaptive Biotechnologies, Seattle, WA 98102, USA.

4. Fred Hutchinson Cancer Research Center, Seattle, WA 98109, USA.

5. Center for Cell Engineering and Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA.

6. Parker Institute for Cancer Immunotherapy, New York, NY 10065, USA.

Abstract

Targeting nonviral antigens in viral-driven cancer Adoptive cell transfer harnesses a patient's own T cells to destroy cancer. The strategy can successfully treat epithelial tumors driven by human papillomavirus (HPV), but it remains unclear why only some patients respond. Stevanović et al. examined the antitumor T cell response associated with HPV + cervical cancers that underwent complete regression. Unexpectedly, reactive T cells were not directed against virally associated antigens, but rather against cancer germline antigens or neoantigens not previously recognized by the immune system. These findings counter the widely held belief that T cell responses against viral antigens are responsible for therapeutic effects in HPV-driven cancers. Science , this issue p. 200

Funder

NCI

Milstein Family Foundation

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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