Bennink J, Effros R B, Doherty P C
Immunology. 1978 Sep;35(3):503-9.
Mice were first primed with a type A or a type B influenza virus and then challenged intranasally at least 1 month later with another type A virus. Potent cytotoxic T cell populations were found in lung, and effector T cell function was also demonstrated in blood, spleen and mediastinal lymph nodes. Lymphocytes isolated from all of these anatomical sites were active against target cells infected with the same, or with serologically different, type A influenza viruses. Also, prior exposure to another type A virus resulted in more rapid development of effector function than was seen in mice that had first been infected with B/Lee. Cytotoxic T cell populations generated in mice with influenza thus tend overall to be type-specific, and there is substantial localization of these effector lymphocytes in the pneumonic lung.
首先用甲型或乙型流感病毒对小鼠进行致敏,然后至少1个月后经鼻内接种另一种甲型病毒进行攻击。在肺中发现了强效细胞毒性T细胞群体,并且在血液、脾脏和纵隔淋巴结中也证明了效应T细胞功能。从所有这些解剖部位分离出的淋巴细胞对感染相同或血清学不同的甲型流感病毒的靶细胞具有活性。此外,与首次感染B/Lee株的小鼠相比,预先接触另一种甲型病毒导致效应功能的发展更快。因此,感染流感的小鼠中产生的细胞毒性T细胞群体总体上倾向于具有型特异性,并且这些效应淋巴细胞大量定位于肺炎肺中。