Department of Hematology and Oncology, Nagoya University Graduate School of Medicine, Japan.
Department of Hematology and Oncology, Nagoya University Graduate School of Medicine, Japan.
Cell Immunol. 2014 Mar-Apr;288(1-2):53-9. doi: 10.1016/j.cellimm.2014.02.007. Epub 2014 Mar 11.
The effect of programmed death 1 (PD-1) on cytomegalovirus (CMV)-specific T cells has not been thoroughly examined. We evaluated the involvement of exhausted CMV-specific T cells in persistent CMV infection after allogeneic hematopoietic stem cell transplantation (HSCT). CMV-specific CD8+ T cells obtained from an HLA-A∗24:02-positive patient, who failed to eliminate CMV for more than 1 year after HSCT, responded poorly to CMV pp65 peptide and showed high PD-1 expression. Sera from patients with persistent CMV infection showed a significantly higher IL-6 level than those from patients with temporary CMV infection after allogeneic HSCT and healthy donors. CD33+ adherent cells produced IL-6, and regulated PD-1 expression and growth of CMV-specific CD8+ T cells through cell-to-cell contact. Although further investigation is required to clarify the association between IL-6 level and CMV infection in more patients, IL-6 might be a useful biomarker of persistent CMV infection after allogeneic HSCT.
PD-1 对巨细胞病毒 (CMV)-特异性 T 细胞的影响尚未得到彻底研究。我们评估了耗竭的 CMV 特异性 T 细胞在异基因造血干细胞移植 (HSCT) 后持续性 CMV 感染中的作用。从一名 HLA-A∗24:02 阳性患者中获得的 CMV 特异性 CD8+T 细胞在 HSCT 后 1 年以上未能消除 CMV,对 CMV pp65 肽的反应较差,并且表现出高水平的 PD-1 表达。与异基因 HSCT 后出现暂时性 CMV 感染的患者和健康供体相比,持续性 CMV 感染患者的血清中 IL-6 水平明显更高。CD33+黏附细胞产生 IL-6,并通过细胞间接触调节 PD-1 表达和 CMV 特异性 CD8+T 细胞的生长。虽然需要进一步研究以在更多患者中阐明 IL-6 水平与 CMV 感染之间的关联,但 IL-6 可能是异基因 HSCT 后持续性 CMV 感染的有用生物标志物。