eLife · 2018 · 87 citations · 37 references
Life SciencesImmunologyOncologyCancer GeneticsImmunogeneticsMolecular OncologyCancer ImmunosurveillanceHuman Leukocyte Antigen SystemMajor Histocompatibility ComplexMalignant NeoplasmsTumor AntigensTumor-associated AntigensClass I Histocompatibility AntigensMajor Histocompatibility Complex (Mhc) PresentationMajor Histocompatibility Complex Class I LossMhc Class I DeficiencyMhc Class I MoleculesTumor Antigen ImmunogenicityTumor ImmunogenicityTumor-host Immune Interactions
), a species which already harbours a more widespread contagious cancer, Devil Facial Tumour 1 (DFT1). Here we show that in contrast to DFT1, DFT2 cells express major histocompatibility complex (MHC) class I molecules, demonstrating that loss of MHC is not necessary for the emergence of a contagious cancer. However, the most highly expressed MHC class I alleles in DFT2 cells are common among host devils or non-polymorphic, reducing immunogenicity in a population sharing these alleles. In parallel, MHC class I loss is emerging in vivo, thus DFT2 may be mimicking the evolutionary trajectory of DFT1. Based on these results we propose that contagious cancers may exploit partial histocompatibility between the tumour and host, but that loss of allogeneic antigens could facilitate widespread transmission of DFT2.
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