Harding C V, Unanue E R
Department of Pathology, Washington University School of Medicine, St Louis, Missouri 63110.
Nature. 1990 Aug 9;346(6284):574-6. doi: 10.1038/346574a0.
The number of specific complexes formed between peptide and the class II major histocompatibility complex (MHC) molecules expressed by an antigen-presenting cell (APC) after exposure to protein antigens is unknown, as is the number that activates T cells. Presentation of foreign peptides by APC takes place when many class II molecules may be occupied by autologous peptides. We have now estimated the number of specific peptide/class II complexes per APC by quantitative immunoprecipitation of I-Ak after pulsing the APC with stimulatory levels of a radioactive immunogenic peptide derived from hen egg-white lysozyme protein. T cells were activated by APC that expressed as few as 210-340 specific peptide/class II complexes (0.1% of the I-Ak molecules). These figures were confirmed using anti-CD3 antibody bound to latex beads as an alternative activating ligand. This low number explains the simultaneous presentation of multiple foreign antigens, even in the face of peptide competition.
抗原呈递细胞(APC)在接触蛋白质抗原后,肽与II类主要组织相容性复合体(MHC)分子形成的特异性复合物数量尚不清楚,激活T细胞的复合物数量也不清楚。当许多II类分子可能被自身肽占据时,APC会呈递外来肽。我们现在通过用源自鸡蛋清溶菌酶蛋白的放射性免疫原性肽的刺激水平脉冲APC后,对I-Ak进行定量免疫沉淀,估计了每个APC上特异性肽/II类复合物的数量。表达低至210 - 340个特异性肽/II类复合物(占I-Ak分子的0.1%)的APC就能激活T细胞。使用结合到乳胶珠上的抗CD3抗体作为替代激活配体,证实了这些数据。这个低数量解释了即使面对肽竞争,多种外来抗原仍能同时呈递的现象。