Süss J
Allerg Immunol (Leipz). 1979;25(3):187-96.
Destruction of influenza virus-infected target cells by cytotoxic, thymus-derived lymphocytes (CTL) and the measurement of this reaction with an 51Cr-release assay is a practicable model for studying the complicated interactions between influenza viruses and T-lymphocytes. There is abundant evidence that T-cell-mediated lysis of influenza virus-infected target cells generally requires the H-2K or H2D region histocompatibility between CTL and target cells. Two general explanation have been proposed to account the requirement of the H-2 compatibility between lymphocytes and virus-infected target cells, the "altered self" concept and the "dual recognition" hypothesis. The specificity of the cytotoxic response against influenza viruses is dependent on the viral haemaglutinin. A second, cross-reactive subpopulation of CTL recognized furthermore the M protein as the traget antigen. The role of the target cells in determining the specificity of the CTL response is therefore of special importance for the infectivity of the influenza viruses.
细胞毒性胸腺来源淋巴细胞(CTL)对流感病毒感染的靶细胞的破坏作用,以及用51Cr释放试验来测定这种反应,是研究流感病毒与T淋巴细胞之间复杂相互作用的一种可行模型。有充分证据表明,T细胞介导的对流感病毒感染靶细胞的裂解作用通常需要CTL与靶细胞之间的H-2K或H2D区域组织相容性。针对淋巴细胞与病毒感染靶细胞之间H-2相容性的需求,已提出两种普遍解释,即“改变的自身”概念和“双重识别”假说。针对流感病毒的细胞毒性反应的特异性取决于病毒血凝素。此外,CTL的第二个交叉反应亚群将M蛋白识别为靶抗原。因此,靶细胞在决定CTL反应特异性方面的作用对于流感病毒的感染性尤为重要。