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         headline:RNA editing derived epitopes function as cancer antigens to elicit immune responses
         description:In addition to genomic mutations, RNA editing is another major mechanism creating sequence variations in proteins by introducing nucleotide changes in mRNA sequences. Deregulated RNA editing contributes to different types of human diseases, including cancers. Here we report that peptides generated as a consequence of RNA editing are indeed naturally presented by human leukocyte antigen (HLA) molecules. We provide evidence that effector CD8+ T cells specific for edited peptides derived from cyclin I are present in human tumours and attack tumour cells that are presenting these epitopes. We show that subpopulations of cancer patients have increased peptide levels and that levels of edited RNA correlate with peptide copy numbers. These findings demonstrate that RNA editing extends the classes of HLA presented self-antigens and that these antigens can be recognised by the immune system. RNA editing is a biological process that creates sequence variation. Here the authors show that peptides generated as a consequence of RNA editing are naturally presented by human leukocyte antigen (HLA) and serve as antigens to elicit anti-tumour immune responses.
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      headline:RNA editing derived epitopes function as cancer antigens to elicit immune responses
      description:In addition to genomic mutations, RNA editing is another major mechanism creating sequence variations in proteins by introducing nucleotide changes in mRNA sequences. Deregulated RNA editing contributes to different types of human diseases, including cancers. Here we report that peptides generated as a consequence of RNA editing are indeed naturally presented by human leukocyte antigen (HLA) molecules. We provide evidence that effector CD8+ T cells specific for edited peptides derived from cyclin I are present in human tumours and attack tumour cells that are presenting these epitopes. We show that subpopulations of cancer patients have increased peptide levels and that levels of edited RNA correlate with peptide copy numbers. These findings demonstrate that RNA editing extends the classes of HLA presented self-antigens and that these antigens can be recognised by the immune system. RNA editing is a biological process that creates sequence variation. Here the authors show that peptides generated as a consequence of RNA editing are naturally presented by human leukocyte antigen (HLA) and serve as antigens to elicit anti-tumour immune responses.
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            address:
               name:Department of Systems Biology, The University of Texas MD Anderson Cancer Center, Houston, USA
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            address:
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            address:
               name:Department of Systems Biology, The University of Texas MD Anderson Cancer Center, Houston, USA
               type:PostalAddress
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            address:
               name:Department of Melanoma Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, USA
               type:PostalAddress
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      email:[email protected]
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      name:Department of Melanoma Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, USA
      name:Immatics Biotechnologies, Tübingen, Germany
      name:Department of Melanoma Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, USA
      name:Department of Melanoma Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, USA
      name:Department of Bioinformatics and Computation Biology, The University of Texas MD Anderson Cancer Center, Houston, USA
      name:Department of Bioinformatics and Computation Biology, The University of Texas MD Anderson Cancer Center, Houston, USA
      name:Immatics US, Houston, USA
      name:Immatics Biotechnologies, Tübingen, Germany
      name:Immatics Biotechnologies, Tübingen, Germany
      name:Immatics Biotechnologies, Tübingen, Germany
      name:Department of Melanoma Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, USA
      name:Department of Melanoma Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, USA
      name:Department of Melanoma Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, USA
      name:Department of Melanoma Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, USA
      name:Department of Biochemistry and Molecular Biology, The University of Texas Health Science Center at Houston McGovern Medical School, Houston, USA
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      name:Department of Systems Biology, The University of Texas MD Anderson Cancer Center, Houston, USA
      name:Department of Melanoma Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, USA

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