Wang Xuelian, Moscicki Anna-Barbara, Tsang Laura, Brockman Andrea, Nakagawa Mayumi
Department of Pathology, College of Medicine, University of Arkansas for Medical Sciences, Little Rock, Arkansas 72205, USA.
Clin Vaccine Immunol. 2008 Jun;15(6):937-45. doi: 10.1128/CVI.00404-07. Epub 2008 Apr 30.
Human papillomavirus (HPV)-specific T-cell response to the HPV type 16 (HPV16) E6 protein has been shown to be associated with successful viral clearance. The patterns of CD8 T-cell epitopes within HPV16 E6 protein were previously studied in two women with HPV16 clearance. The goal of this study was to characterize these epitopes in terms of their minimal and optimal amino acid sequences and the human leukocyte antigen (HLA) restriction molecules. The presence of the epitope-specific memory T cells after viral clearance was also examined. In subject A, the dominant epitope was characterized to be E6 75-83 (KFYSKISEY), restricted by the HLA-B62 molecule, while that of subject B was E6 133-142 (HNIRGRWTGR), restricted by the HLA-A6801 molecule. Homologous epitopes were identified in five other high-risk HPV types for both of these epitopes, but they were not recognized by respective T-cell clone cells. An enzyme-linked immunospot assay or tetramer analysis was performed on peripheral blood mononuclear cells from blood samples collected after viral clearance but prior to isolation of the T-cell clones. The presence of epitope-specific memory T cells was demonstrated. These data suggest that HPV-specific memory T cells were generated in vivo and that they may remain in circulation many months, if not years, after viral clearance. Our findings broaden the spectrum of the CD8 T-cell epitopes of the HPV16 E6 protein. The characterization of novel T-cell epitopes and long-lasting epitope-specific memory T cells may be useful for the development of a potential epitope-based vaccine.
人乳头瘤病毒(HPV)对16型人乳头瘤病毒(HPV16)E6蛋白的特异性T细胞反应已被证明与病毒的成功清除有关。先前在两名HPV16清除者中研究了HPV16 E6蛋白内CD8 T细胞表位的模式。本研究的目的是根据其最小和最佳氨基酸序列以及人类白细胞抗原(HLA)限制性分子来表征这些表位。还检测了病毒清除后表位特异性记忆T细胞的存在。在受试者A中,主要表位被表征为E6 75 - 83(KFYSKISEY),受HLA - B62分子限制,而受试者B的主要表位为E6 133 - 142(HNIRGRWTGR),受HLA - A6801分子限制。在其他五种高危HPV类型中鉴定出了这两种表位的同源表位,但它们未被各自的T细胞克隆细胞识别。对病毒清除后但在分离T细胞克隆之前采集的血样中的外周血单核细胞进行了酶联免疫斑点测定或四聚体分析。证实了表位特异性记忆T细胞的存在。这些数据表明,HPV特异性记忆T细胞在体内产生,并且在病毒清除后可能会在循环中存留数月甚至数年。我们的发现拓宽了HPV16 E6蛋白CD8 T细胞表位的范围。新型T细胞表位和持久的表位特异性记忆T细胞的表征可能有助于开发潜在的基于表位的疫苗。