Hussey Kathryn, Caldwell Alison, Kreiss Alexandre, Skjødt Karsten, Gastaldello Annalisa, Pye Ruth, Hamede Rodrigo, Woods Gregory M, Siddle Hannah V
School of Biological Sciences, University of Southampton, Southampton SO17 1BJ, UK.
Menzies Institute for Medical Research, University of Tasmania, Hobart, TAS 7000, Australia.
Pathogens. 2022 Mar 14;11(3):351. doi: 10.3390/pathogens11030351.
Devil facial tumour disease (DFTD) is a transmissible cancer that has circulated in the Tasmanian devil population for >25 years. Like other contagious cancers in dogs and devils, the way DFTD escapes the immune response of its host is a central question to understanding this disease. DFTD has a low major histocompatibility complex class I (MHC-I) expression due to epigenetic modifications, preventing host immune recognition of mismatched MHC-I molecules by T cells. However, the total MHC-I loss should result in natural killer (NK) cell activation due to the ‘missing self’. Here, we have investigated the expression of the nonclassical MHC-I, Saha-UD as a potential regulatory or suppressive mechanism for DFTD. A monoclonal antibody was generated against the devil Saha-UD that binds recombinant Saha-UD by Western blot, with limited crossreactivity to the classical MHC-I, Saha-UC and nonclassical Saha-UK. Using this antibody, we confirmed the expression of Saha-UD in 13 DFTD tumours by immunohistochemistry (n = 15) and demonstrated that Saha-UD expression is heterogeneous, with 12 tumours showing intratumour heterogeneity. Immunohistochemical staining for the Saha-UD showed distinct patterns of expression when compared with classical MHC-I molecules. The nonclassical Saha-UD expression by DFTD tumours in vivo may be a mechanism for immunosuppression, and further work is ongoing to characterise its ligand on immune cells.
袋獾面部肿瘤病(DFTD)是一种可传播的癌症,已在袋獾种群中传播了超过25年。与犬类和袋獾中的其他传染性癌症一样,DFTD逃避宿主免疫反应的方式是理解这种疾病的核心问题。由于表观遗传修饰,DFTD的主要组织相容性复合体I类(MHC-I)表达较低,从而阻止宿主T细胞对不匹配的MHC-I分子进行免疫识别。然而,MHC-I的完全缺失应会因“自我缺失”而导致自然杀伤(NK)细胞激活。在此,我们研究了非经典MHC-I Saha-UD的表达,将其作为DFTD的一种潜在调节或抑制机制。制备了一种针对袋獾Saha-UD的单克隆抗体,该抗体通过蛋白质印迹法与重组Saha-UD结合,与经典MHC-I Saha-UC和非经典Saha-UK的交叉反应有限。使用该抗体,我们通过免疫组织化学在13个DFTD肿瘤中证实了Saha-UD的表达(n = 15),并证明Saha-UD表达具有异质性,12个肿瘤显示肿瘤内异质性。与经典MHC-I分子相比,Saha-UD的免疫组织化学染色显示出不同的表达模式。DFTD肿瘤在体内的非经典Saha-UD表达可能是一种免疫抑制机制,目前正在进一步开展工作以鉴定其在免疫细胞上的配体。