Duprez V, Hénin Y, Lévy J P
J Immunol Methods. 1980;37(3-4):249-60. doi: 10.1016/0022-1759(80)90311-7.
Lymphoma cells induced in vivo by exogenous C type viruses are usually used as target cells to test the activity of cytolytic T lymphocytes (CTL) directed against the virus-induced cell surface FMR antigen. Such lymphomas are available only in a small number of inbred strains of mice, thus setting limits to the study of H-2 antigens in the interaction between CTL and tumor target cells. A method is proposed to overcome this, using mitogen-induced blast cells from adult mice neonatally infected with C type viruses. Such blast cells bear serologically detectable viral antigens and function as convenient targets in the chromium release test, as well as competitor cells or stimulator cells in vitro. With this method it has been possible to study T cell-mediated anti-FMR reactions in 12 different inbred strains of mice bearing 10 different H-2 haplotypes. The same method could probably be used in any inbred strain, greatly improving the possibility of immunogenetic studies in C type virus systems.
由外源性C型病毒在体内诱导产生的淋巴瘤细胞通常用作靶细胞,以检测针对病毒诱导的细胞表面FMR抗原的细胞溶解T淋巴细胞(CTL)的活性。此类淋巴瘤仅在少数近交系小鼠中存在,因此限制了在CTL与肿瘤靶细胞相互作用中对H-2抗原的研究。本文提出了一种克服这一问题的方法,即使用新生期感染C型病毒的成年小鼠经丝裂原诱导产生的母细胞。此类母细胞带有血清学上可检测到的病毒抗原,在铬释放试验中作为方便的靶细胞,以及在体外作为竞争细胞或刺激细胞。通过这种方法,已经能够在携带10种不同H-2单倍型的12种不同近交系小鼠中研究T细胞介导的抗FMR反应。同样的方法可能适用于任何近交系,极大地提高了在C型病毒系统中进行免疫遗传学研究的可能性。