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释放病毒感染中 HLA 等位基因特异性肽锚的概念:一种非经典的天然人巨细胞病毒衍生的 HLA-A*24:02 限制性肽引发高度免疫原性。

Releasing the concept of HLA-allele specific peptide anchors in viral infections: A non-canonical naturally presented human cytomegalovirus-derived HLA-A*24:02 restricted peptide drives exquisite immunogenicity.

机构信息

Institute for Transfusion Medicine, Hannover Medical School, Hannover, Germany.

Department of Cellular Logistics, Max Planck Institute for Biophysical Chemistry, Göttingen, Germany.

出版信息

HLA. 2019 Jul;94(1):25-38. doi: 10.1111/tan.13537. Epub 2019 Apr 14.

Abstract

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.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5170/6593758/6070c13f7add/TAN-94-25-g001.jpg

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