Sester Martina, Sester Urban, Gärtner Barbara, Kubuschok Boris, Girndt Matthias, Meyerhans Andreas, Köhler Hans
Medical Department IV, Institute of Medical Microbiology and Hygiene, University of the Saarland, D-66421 Homburg, Germany.
J Virol. 2002 Apr;76(8):3748-55. doi: 10.1128/jvi.76.8.3748-3755.2002.
Replication of cytomegalovirus (CMV) is largely controlled by the cellular arm of the immune response. In this study the CMV-specific CD4 T-cell response was characterized in a cohort of apparently healthy individuals. In 11% of all individuals, extremely high frequencies, between 10 and 40%, were found. High-level frequencies of CMV-specific CD4 T cells persisted over several months and were not the result of an acute infection. Specific T cells were oligoclonal and were phenotypically and functionally characterized as mature effector cells, with both cytokine-secreting and proliferative potential. These high-level frequencies do not seem to compromise the immune response towards heterologous infections, and no signs of immunopathology were observed. Whereas a large temporary expansion of virus-specific T cells is well known to occur during acute infection, we now show that extremely high frequencies of virus-specific T cells may continuously exist in chronic CMV infection without overtly compromising the remaining protective immunity.
巨细胞病毒(CMV)的复制在很大程度上受免疫反应的细胞分支控制。在本研究中,对一组看似健康的个体的CMV特异性CD4 T细胞反应进行了表征。在所有个体的11%中,发现频率极高,在10%至40%之间。CMV特异性CD4 T细胞的高频率持续数月,并非急性感染的结果。特异性T细胞是寡克隆的,在表型和功能上被表征为成熟效应细胞,具有分泌细胞因子和增殖的潜力。这些高频率似乎不会损害对异源感染的免疫反应,也未观察到免疫病理学迹象。虽然众所周知,在急性感染期间会发生病毒特异性T细胞的大量暂时扩增,但我们现在表明,在慢性CMV感染中可能持续存在极高频率的病毒特异性T细胞,而不会明显损害其余的保护性免疫。