Zinkernagel R M, Oldstone M B
Proc Natl Acad Sci U S A. 1976 Oct;73(10):3666-70. doi: 10.1073/pnas.73.10.3666.
Murine F9 teratoma cells do not express major transplantation antigens detectable by either serologic or alloreactive assays of thymus-dependent lymphocytes (T cells). Such cells can be infected with lymphocytic choriomeningitis virus or vaccinia virus, do express viral antigens on the cell surface, and can release infectious virus in amounts equivalent to those of other H-2 bearing murine cell lines. Immunologic injury of virus-infected F9 cells occurs after the addition of specific antiviral antibody and complement or of specific antiviral antibody and unsensitized lymphoid cells (antibody-mediated cell-dependent killing). In contrast, injury does not follow the addition of immune cytotoxic T cells. These results indicate that possession of H-2 antigens is not a requirement for a cell's infection by or production of virus. Further, expression of viral antigens on the cell's surface, although adequate for antibody-mediated immune injury, is by itself insufficient for direct T cell-mediated lysis. The major transplantation antigens thus probably represent the cell surface structures that are crucial for T-mediated cell wall damage that results in chromium release.
小鼠F9畸胎瘤细胞不表达可通过胸腺依赖性淋巴细胞(T细胞)的血清学或同种异体反应性检测法检测到的主要移植抗原。此类细胞可被淋巴细胞性脉络丛脑膜炎病毒或痘苗病毒感染,确实在细胞表面表达病毒抗原,并且能释放与其他带有H-2的小鼠细胞系数量相当的传染性病毒。在加入特异性抗病毒抗体和补体或特异性抗病毒抗体和未致敏的淋巴细胞后(抗体介导的细胞依赖性杀伤),病毒感染的F9细胞会发生免疫损伤。相比之下,加入免疫细胞毒性T细胞后不会出现损伤。这些结果表明,拥有H-2抗原并非细胞被病毒感染或产生病毒的必要条件。此外,病毒抗原在细胞表面的表达,虽然足以介导抗体介导的免疫损伤,但自身不足以介导直接的T细胞介导的裂解。因此,主要移植抗原可能代表了对T介导的导致铬释放的细胞壁损伤至关重要的细胞表面结构。