Berkhoff Eufemia G M, Geelhoed-Mieras Martina M, Jonges Marcel, Smith Derek J, Fouchier Ron A M, Osterhaus Albert D M E, Rimmelzwaan Guus F
Department of Virology and Postgraduate School Molecular Medicine, Erasmus Medical Center, Rotterdam, The Netherlands.
Virus Res. 2007 Jun;126(1-2):282-7. doi: 10.1016/j.virusres.2007.02.018. Epub 2007 Apr 8.
Influenza virus-specific CD4+ T-helper cells were cloned that recognized a virus strain isolated in 1981, but that failed to recognize more recent strains. The HLA-DR*1601-restricted epitope recognized was located in the hemagglutinin (HA(99-113)) and the naturally occurring A-->V substitution at position 106 was responsible for abrogating the recognition by HA(99-113)-specific CD4+ T-cells. This amino acid substitution was found in influenza A/H3N2 viruses that circulated between 1999 and 2005 and did not affect recognition by virus-specific antibodies. It was speculated that influenza viruses could evade recognition by virus-specific CD4+ T-cells, at least temporarily.
克隆出了流感病毒特异性CD4 +辅助性T细胞,这些细胞能识别1998年分离出的一种病毒株,但无法识别更新的病毒株。所识别的HLA - DR*1601限制性表位位于血凝素(HA(99 - 113))中,第106位天然发生的A→V取代导致HA(99 - 113)特异性CD4 + T细胞无法识别。在1999年至2005年间传播的甲型H3N2流感病毒中发现了这种氨基酸取代,且它不影响病毒特异性抗体的识别。据推测,流感病毒至少能暂时逃避病毒特异性CD4 + T细胞的识别。