作者
Asolina Braun,Louise C. Rowntree,Ziyi Huang,Kirti Pandey,Nikolas Thuesen,Chen Li,Jan Petersen,Dene R. Littler,Shabana Raji,Thi H. O. Nguyen,Emma Jappe Lange Jappe Lange,Gry Persson,Michael Schantz Klausen,Jens Vindahl Kringelum,Shanzou Chung,Nathan P. Croft,Pouya Faridi,Rochelle Ayala,Jamie Rossjohn,Patricia T. Illing,Katherine E. Scull,Sri H. Ramarathinam,Nicole A. Mifsud,Katherine Kedzierska,Anders Bundgård Sørensen,Anthony W. Purcell
摘要
Most COVID-19 vaccines elicit immunity against the SARS-CoV-2 Spike protein. However, Spike protein mutations in emerging strains and immune evasion by the SARS-CoV-2 virus demonstrates the need to develop more broadly targeting vaccines. To facilitate this, we use mass spectrometry to identify immunopeptides derived from seven relatively conserved structural and non-structural SARS-CoV-2 proteins (N, E, Nsp1/4/5/8/9). We use two different B-lymphoblastoid cell lines to map Human Leukocyte Antigen (HLA) class I and class II immunopeptidomes covering some of the prevalent HLA types across the global human population. We employ DNA plasmid transfection and direct antigen delivery approaches to sample different antigens and find 248 unique HLA class I and HLA class II bound peptides with 71 derived from N, 12 from E, 28 from Nsp1, 19 from Nsp4, 73 from Nsp8 and 45 peptides derived from Nsp9. Over half of the viral peptides are unpublished. T cell reactivity tested against 56 of the detected peptides shows CD8