Recognition of a Ubiquitous Self Antigen by Prostate Cancer-Infiltrating CD8 + T Lymphocytes

Author:

Savage Peter A.12345,Vosseller Keith12345,Kang Chulho12345,Larimore Kevin12345,Riedel Elyn12345,Wojnoonski Kathleen12345,Jungbluth Achim A.12345,Allison James P.12345

Affiliation:

1. Department of Immunology, Howard Hughes Medical Institute, and Ludwig Center for Cancer Immunotherapy, Memorial Sloan-Kettering Cancer Center (MSKCC), New York, NY 10021, USA.

2. Department of Biochemistry and Molecular Biology, Drexel University College of Medicine, Philadelphia, PA 19102, USA.

3. Cancer Research Laboratory, University of California, Berkeley, CA 94720, USA.

4. Department of Molecular and Cell Biology, University of California, Berkeley, CA 94720, USA.

5. Department of Epidemiology and Biostatistics, MSKCC, New York, NY 10065, USA.

Abstract

Substantial evidence exists that many tumors can be specifically recognized by CD8 + T lymphocytes. The definition of antigens targeted by these cells is paramount for the development of effective immunotherapeutic strategies for treating human cancers. In a screen for endogenous tumor-associated T cell responses in a primary mouse model of prostatic adenocarcinoma, we identified a naturally arising CD8 + T cell response that is reactive to a peptide derived from histone H4. Despite the ubiquitous nature of histones, T cell recognition of histone H4 peptide was specifically associated with the presence of prostate cancer in these mice. Thus, the repertoire of antigens recognized by tumor-infiltrating T cells is broader than previously thought and includes peptides derived from ubiquitous self antigens that are normally sequestered from immune detection.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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