Department of Immunology, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA.
Center for Systems Immunology, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA.
Nat Methods. 2021 Aug;18(8):873-880. doi: 10.1038/s41592-020-0867-z. Epub 2020 Jul 6.
T cells respond to threats in an antigen-specific manner using T cell receptors (TCRs) that recognize short peptide antigens presented on major histocompatibility complex (MHC) proteins. The TCR-peptide-MHC interaction mediated between a T cell and its target cell dictates its function and thereby influences its role in disease. A lack of approaches for antigen discovery has limited the fundamental understanding of the antigenic landscape of the overall T cell response. Recent advances in high-throughput sequencing, mass cytometry, microfluidics and computational biology have led to a surge in approaches to address the challenge of T cell antigen discovery. Here, we summarize the scope of this challenge, discuss in depth the recent exciting work and highlight the outstanding questions and remaining technical hurdles in this field.
T 细胞通过 T 细胞受体(TCR)以抗原特异性的方式对威胁作出反应,TCR 识别主要组织相容性复合体(MHC)蛋白上呈现的短肽抗原。T 细胞与其靶细胞之间的 TCR-肽-MHC 相互作用决定了其功能,从而影响其在疾病中的作用。由于缺乏抗原发现方法,限制了对整个 T 细胞反应的抗原景观的基本理解。高通量测序、质谱细胞术、微流控和计算生物学的最新进展,为解决 T 细胞抗原发现的挑战提供了大量的方法。在这里,我们总结了这一挑战的范围,深入讨论了最近令人兴奋的工作,并强调了该领域的突出问题和遗留的技术障碍。