Cellular Biology Section, Laboratory of Viral Diseases, NIAID, Bethesda, MD, United States.
Cellular Biology Section, Laboratory of Viral Diseases, NIAID, Bethesda, MD, United States.
Mol Immunol. 2019 Sep;113:38-42. doi: 10.1016/j.molimm.2017.12.026. Epub 2018 Jan 17.
The MHC class I antigen presentation pathway enables T cell immunosurveillance of cancer cells, viruses and other intracellular pathogens. Rapidly degraded newly synthesized proteins (DRiPs) are a major source of self-, and particularly, viral antigenic peptides. A number of findings support the idea that a substantial fraction of antigenic peptides are synthesized by "immunoribosomes", a subset of translating ribosomes that generate class I peptides with enhanced efficiency. Here, we review the evidence for the immunoribosome hypothesis.
MHC I 类抗原呈递途径使 T 细胞能够对癌细胞、病毒和其他细胞内病原体进行免疫监视。快速降解的新合成蛋白 (DRiPs) 是自身抗原肽,尤其是病毒抗原肽的主要来源。许多研究结果支持这样一种观点,即大量抗原肽是由“免疫核糖体”合成的,免疫核糖体是翻译核糖体的一个子集,能够以更高的效率生成 I 类肽。本文综述了免疫核糖体假说的证据。