Institute for Transfusion Medicine, Hannover Medical School, Hannover, Germany.
Department of Cellular Logistics, Max Planck Institute for Biophysical Chemistry, Göttingen, Germany.
HLA. 2019 Jul;94(1):25-38. doi: 10.1111/tan.13537. Epub 2019 Apr 14.
T-cell receptors possess the unique ability to survey and respond to their permanently modified ligands, self HLA-I molecules bound to non-self peptides of various origin. This highly specific immune function is impaired following hematopoietic stem cell transplantation (HSCT) for a timespan of several months needed for the maturation of T-cells. Especially, the progression of HCMV disease in immunocompromised patients induces life-threatening situations. Therefore, the need for a new immune system that delivers vital and potent CD8+ T-cells carrying TCRs that recognize even one human cytomegalovirus (HCMV) peptide/HLA molecule and clear the viral infection long term becomes obvious. The transcription and translation of HCMV proteins in the lytic cycle is a precisely regulated cascade of processes, therefore, it is a highly sensitive challenge to adjust the exact time point of HCMV-peptide recruitment over self-peptides. We utilized soluble HLA technology in HCMV-infected fibroblasts and sequenced naturally sHLA-A*24:02 presented HCMV-derived peptides. One peptide of 14 AAs length derived from the IE2 antigen induced the strongest T-cell responses; this peptide can be detected with a low ranking score in general peptide prediction databanks. These results highlight the need for elaborate and HLA-allele specific peptide selection.
T 细胞受体具有独特的能力,可以对其永久修饰的配体(与各种来源的非自身肽结合的自身 HLA-I 分子)进行检测和响应。这种高度特异性的免疫功能在接受造血干细胞移植(HSCT)后会受到损害,因为 T 细胞需要几个月的时间才能成熟。特别是,免疫功能低下患者的 HCMV 疾病进展会导致危及生命的情况。因此,需要一种新的免疫系统,能够提供携带 TCR 的重要和有效的 CD8+ T 细胞,这些 TCR 能够识别甚至一种人类巨细胞病毒(HCMV)肽/HLA 分子,并长期清除病毒感染,这一点变得显而易见。在裂解周期中,HCMV 蛋白的转录和翻译是一个精确调节的级联过程,因此,精确调整 HCMV 肽招募相对于自身肽的时间点是一个高度敏感的挑战。我们在 HCMV 感染的成纤维细胞中利用可溶性 HLA 技术,并对天然存在的 sHLA-A*24:02 呈递的 HCMV 衍生肽进行测序。一个 14 个氨基酸长度的来自 IE2 抗原的肽诱导了最强的 T 细胞反应;该肽在一般肽预测数据库中可以用低排名分数检测到。这些结果强调了需要进行精心设计和 HLA 等位基因特异性肽选择。