Kees U, Krammer P H
J Exp Med. 1984 Feb 1;159(2):365-77. doi: 10.1084/jem.159.2.365.
This paper shows that most murine (C57BL/6) influenza A virus-specific memory cytotoxic T lymphocyte (CTL) clones tested in limiting dilution did not react with the influenza A virus surface glycoproteins, hemagglutinin (HA) and neuraminidase (NA). This lysis of syngeneic target cells infected with the influenza A virus strains, Aichi (H3N2), PR8 (H1N1), or recombinant strain X31 (H3N2) indicates that most antigenic epitopes recognized are associated with internal virus determinants. X31 and PR8 share the internal, and X31 and Aichi the external, viral determinants. Extensive CTL cross-reactivity was observed in experiments with target cells infected with virus carrying internal determinants homologous with the priming virus. In contrast, when the internal viral determinants differed between the priming virus and the virus used to infect the target cells, and although HA and NA were homologous, we found almost complete CTL-specificity for the priming virus. Thus, the predominant reactivity of influenza A virus-specific CTL differs from that of anti-influenza A antibodies, which are primarily directed towards epitopes on the virus surface glycoproteins. This finding may be relevant for the role of influenza A virus-specific CTL in recurrent infections with different influenza A viruses.
本文表明,在有限稀释实验中测试的大多数鼠源(C57BL/6)甲型流感病毒特异性记忆细胞毒性T淋巴细胞(CTL)克隆不与甲型流感病毒表面糖蛋白血凝素(HA)和神经氨酸酶(NA)发生反应。对感染甲型流感病毒株(如爱知株(H3N2)、PR8株(H1N1)或重组株X31(H3N2))的同基因靶细胞的这种裂解表明,所识别的大多数抗原表位与病毒内部决定簇相关。X31和PR8共享内部病毒决定簇,X31和爱知株共享外部病毒决定簇。在用携带与引发病毒同源的内部决定簇的病毒感染的靶细胞进行的实验中观察到广泛的CTL交叉反应性。相反,当引发病毒和用于感染靶细胞的病毒之间的内部病毒决定簇不同,并且尽管HA和NA是同源的时,我们发现对引发病毒几乎完全具有CTL特异性。因此,甲型流感病毒特异性CTL的主要反应性不同于抗甲型流感抗体,后者主要针对病毒表面糖蛋白上的表位。这一发现可能与甲型流感病毒特异性CTL在不同甲型流感病毒反复感染中的作用有关。