Chang Jun, Braciale Thomas J
Beirne B. Carter Center for Immunology Research, University of Virginia Health Sciences Center, Charlottesville, Virginia, USA.
Nat Med. 2002 Jan;8(1):54-60. doi: 10.1038/nm0102-54.
Respiratory syncytial virus (RSV) is a major cause of morbidity from respiratory infection in infants, young children and the elderly. No effective vaccine against RSV is currently available and studies of the natural history of RSV infection suggest repeated infections with antigenically related virus strains are common throughout an individual's lifetime. We have studied the CD8+ T-cell response during experimental murine RSV infection and found that RSV inhibits the expression of effector activity by activated RSV-specific CD8+ T cells infiltrating the lung parenchyma and the development of pulmonary CD8+ T-cell memory by interfering with TCR-mediated signaling. These data suggest a possible mechanism to explain the limited duration of protective immunity in RSV infection.
呼吸道合胞病毒(RSV)是导致婴儿、幼儿和老年人发生呼吸道感染而发病的主要原因。目前尚无针对RSV的有效疫苗,对RSV感染自然史的研究表明,在个体一生中,反复感染抗原相关病毒株的情况很常见。我们研究了实验性小鼠RSV感染期间的CD8 + T细胞反应,发现RSV通过干扰TCR介导的信号传导,抑制浸润肺实质的活化RSV特异性CD8 + T细胞的效应活性表达以及肺CD8 + T细胞记忆的形成。这些数据提示了一种可能的机制,用以解释RSV感染中保护性免疫持续时间有限的现象。