Centre for Inflammation Biology and Cancer Immunology (CIBCI) & Peter Gorer Department of Immunobiology, King's College London, London, United Kingdom; Francis Crick Institute, London, United Kingdom.
Mol Cell Proteomics. 2021;20:100158. doi: 10.1016/j.mcpro.2021.100158. Epub 2021 Oct 2.
Proteasome-generated spliced epitopes presented by HLA class I complexes are emerging targets for T cell targeted immunotherapies. Their identification by mass spectrometry triggered heated debates, which find a representative opinion in one of the two fronts in the recent perspective article by Arie Admon. Briefly, he suggests that proteasomes cannot efficiently catalyze such a reaction, and, thus, that all spliced peptides identified in HLA class I immunopeptidomes and other specimens are artifacts. This hypothesis is in contrast with in vitro, in cellula, and in vivo results published since the discovery of proteasome-catalyzed peptide splicing in 2004.
蛋白酶体生成的由 HLA Ⅰ类复合物呈递的剪接表位是 T 细胞靶向免疫疗法的新兴靶点。通过质谱鉴定这些表位引发了激烈的争论,在 Arie Admon 最近的观点文章中,其中一个前沿观点可以代表这一争论。简而言之,他认为蛋白酶体不能有效地催化这种反应,因此,在 HLA Ⅰ类免疫肽组和其他样本中鉴定的所有剪接肽都是人为产物。这一假说与自 2004 年发现蛋白酶体催化肽剪接以来发表的体外、细胞内和体内结果相悖。